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      • Princeton, New Jersey
      • Temp to Perm
      • $40.00 per hour
      • 9:00 AM - 6:00 PM
      Summary:- Technical Analyst I, Xcellerate Customer Success - Medical Review (XMR)- The Analyst I is a member of Xcellerate Monitoring Integration and Configuration Services (XMICS), part of Monitoring and Data Flow Optimization Team and global risk based monitoring team and supports execution of several key Risk Based Monitoring (RBM) data integration, standard mapping and tool configuration and customization activities and operates as a supporting XMICS Analyst for assigned studies.- The Analyst I collaborates with the study team to define configuration plans, map operational and clinical data, set up central monitoring tools and dashboards to comply with the central monitoring configuration plans.- The Analyst I requires working knowledge of two or more areas of programming - Must have Python knowledge - (e.g. clinical data structures and mapping, tool configuration and JSON, JavaScript or HTML5 programming) as well as a working knowledge of broader drug development and clinical trials. He/she is responsible for accurate and timely uploading of operational and clinical trial data and refresh of central monitoring dashboards and tools.- The Analyst I may provide RBM tool expertise to the study team.- The Analyst I will support Xcellerate Monitoring, RBM and central monitoring integration and configuration services for at least 2 clinical studies.Responsibilities:Job Responsibilities:Work with senior management, technical and client teams in order to determine data requirements, business data implementation approaches, best practices for advanced data manipulation, storage and analysis strategies Write and code logical and physical database descriptions and specify identifiers of database to management system or direct others in coding descriptions Design, implement, automate and maintain large scale enterprise data ETL processes Modify existing databases and database management systems and/or direct programmers and analysts to make changes Test programs or databases, correct errors and make necessary modifications.Working hours: 9:00 AM - 6:00 PMSkills:The main function of a data analyst is to coordinate changes to computer databases, test, and implement the database applying knowledge of database management systems.Education:BachelorsExperience:1-4 yearsQualifications:- Bachelor's degree in a technical field such as computer science, computer engineering or related field required- 2-4 years applicable experience required- Experience with database technologies Knowledge of the ETL process- Knowledge of at least one scripting language- Strong written and oral communication skills- Strong troubleshooting and problem solving skills- Demonstrated history of success Desire to be working with data and helping businesses make better data driven decisions Benefits and Compensation:Temp - PermIn-office: Princeton, NJMonday - Friday 8-5/9-6$40/hr.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Summary:- Technical Analyst I, Xcellerate Customer Success - Medical Review (XMR)- The Analyst I is a member of Xcellerate Monitoring Integration and Configuration Services (XMICS), part of Monitoring and Data Flow Optimization Team and global risk based monitoring team and supports execution of several key Risk Based Monitoring (RBM) data integration, standard mapping and tool configuration and customization activities and operates as a supporting XMICS Analyst for assigned studies.- The Analyst I collaborates with the study team to define configuration plans, map operational and clinical data, set up central monitoring tools and dashboards to comply with the central monitoring configuration plans.- The Analyst I requires working knowledge of two or more areas of programming - Must have Python knowledge - (e.g. clinical data structures and mapping, tool configuration and JSON, JavaScript or HTML5 programming) as well as a working knowledge of broader drug development and clinical trials. He/she is responsible for accurate and timely uploading of operational and clinical trial data and refresh of central monitoring dashboards and tools.- The Analyst I may provide RBM tool expertise to the study team.- The Analyst I will support Xcellerate Monitoring, RBM and central monitoring integration and configuration services for at least 2 clinical studies.Responsibilities:Job Responsibilities:Work with senior management, technical and client teams in order to determine data requirements, business data implementation approaches, best practices for advanced data manipulation, storage and analysis strategies Write and code logical and physical database descriptions and specify identifiers of database to management system or direct others in coding descriptions Design, implement, automate and maintain large scale enterprise data ETL processes Modify existing databases and database management systems and/or direct programmers and analysts to make changes Test programs or databases, correct errors and make necessary modifications.Working hours: 9:00 AM - 6:00 PMSkills:The main function of a data analyst is to coordinate changes to computer databases, test, and implement the database applying knowledge of database management systems.Education:BachelorsExperience:1-4 yearsQualifications:- Bachelor's degree in a technical field such as computer science, computer engineering or related field required- 2-4 years applicable experience required- Experience with database technologies Knowledge of the ETL process- Knowledge of at least one scripting language- Strong written and oral communication skills- Strong troubleshooting and problem solving skills- Demonstrated history of success Desire to be working with data and helping businesses make better data driven decisions Benefits and Compensation:Temp - PermIn-office: Princeton, NJMonday - Friday 8-5/9-6$40/hr.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Raleigh, North Carolina
      • Temp to Perm
      • $16.00 per hour
      • Various Shifts Available
      Join the Biotech movement in North Carolina!As one of the key people in the manufacturing and packaging process you will be involved in various steps.Responsibilities:- The operator???s responsibilities include inspecting and packaging of terminally sterilized and aseptically produced pharmaceutical drugs in accordance with current Good Manufacturing Practices- Operate packaging equipment to package production within all applicable SOPS, cGMPs, etc- Operate equipment within the validated parameters- Perform 100% final inspection of units- Label and package acceptable units- Follow and maintain documentation records, accountability of solution and units throughout the production process- Check and verify components- Perform quality control duties, i.e. sampling of product and environment- Clean/sanitize production and warehouse areas and equipment- Work safely in accordance with regulations, standards, and procedures and in a manner that eliminates unreasonable risk to health and the environment- Notify management of unsafe conditions or practices, unlawful activities and activities which present unreasonable health and/or environmental risk- Report all safety and/or environmental incidents to management immediately- Special projects: training required for returned goods, reclaim and off-line projects- Other duties as assigned with or without accommodation- Responsible for quality of product- Responsible for monitoring the process and documenting measurements per SOPWorking hours: Various Shifts AvailableSkills:- Operator must understand and adhere to standard operating procedures (SOP's) in a pharmaceutical manufacturing environment and be able to apply Good Manufacturing Practices- This position also requires successful completion of the training/certification program- Responsible for reducing product losses and improving yields- Responsible for participation in all Safety aspects of the plant- Responsible for demonstrating initiative, self-direction and ability to make decisions- Responsible for demonstrating and support of company policies- Able to work flexible hours- Requires high degree on manual dexterity, which could be performed under restrictive conditions- Mental and visual accuracy is a demand to produce quality product- Responsible for good verbal and interpersonal skills in communication- Make sound decisions and have good math and reading skillsEducation:High SchoolExperience:1-4 yearsQualifications:- 1-3 years pharmaceutical manufacturing experience within a sterile environment (i.e. ISO 5E or similar)- Ability to work both on a team and individually Great opportunity to get started in biotech! Apply today for more informationSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Join the Biotech movement in North Carolina!As one of the key people in the manufacturing and packaging process you will be involved in various steps.Responsibilities:- The operator???s responsibilities include inspecting and packaging of terminally sterilized and aseptically produced pharmaceutical drugs in accordance with current Good Manufacturing Practices- Operate packaging equipment to package production within all applicable SOPS, cGMPs, etc- Operate equipment within the validated parameters- Perform 100% final inspection of units- Label and package acceptable units- Follow and maintain documentation records, accountability of solution and units throughout the production process- Check and verify components- Perform quality control duties, i.e. sampling of product and environment- Clean/sanitize production and warehouse areas and equipment- Work safely in accordance with regulations, standards, and procedures and in a manner that eliminates unreasonable risk to health and the environment- Notify management of unsafe conditions or practices, unlawful activities and activities which present unreasonable health and/or environmental risk- Report all safety and/or environmental incidents to management immediately- Special projects: training required for returned goods, reclaim and off-line projects- Other duties as assigned with or without accommodation- Responsible for quality of product- Responsible for monitoring the process and documenting measurements per SOPWorking hours: Various Shifts AvailableSkills:- Operator must understand and adhere to standard operating procedures (SOP's) in a pharmaceutical manufacturing environment and be able to apply Good Manufacturing Practices- This position also requires successful completion of the training/certification program- Responsible for reducing product losses and improving yields- Responsible for participation in all Safety aspects of the plant- Responsible for demonstrating initiative, self-direction and ability to make decisions- Responsible for demonstrating and support of company policies- Able to work flexible hours- Requires high degree on manual dexterity, which could be performed under restrictive conditions- Mental and visual accuracy is a demand to produce quality product- Responsible for good verbal and interpersonal skills in communication- Make sound decisions and have good math and reading skillsEducation:High SchoolExperience:1-4 yearsQualifications:- 1-3 years pharmaceutical manufacturing experience within a sterile environment (i.e. ISO 5E or similar)- Ability to work both on a team and individually Great opportunity to get started in biotech! Apply today for more informationSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Madison, Wisconsin
      • Temporary
      • $20.00 - $22.00 per hour
      • 8:00 AM - 5:00 PM
      This position can be REMOTE!Spherion is recruiting a Quality Systems Project Associate! In this position, you will be an integral member of the team dedicated to assisting our client in maintaining compliance with key quality system processes.Responsibilities:- Support key day-to-day tasks within the supplier quality team, including supplier change notifications, supplier approvals, and direct material approvals- Perform project assignments to support the supplier quality organization- Modify and create procedures, forms, and records necessary for the quality system- Complete actions assigned from audits, deviations, changes, nonconformances, etc.- Assist in the creation of metrics applicable to review processes and report results and suggestions to management or other stakeholders- Represent the Quality System team in projects, as assigned- Work with QS and/or other process or business leaders on urgent/critical activities or corrective actions needed for the businessWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent organizational skills- Advanced PC skills to include proficiency in Word, Excel, SharePoint, Outlook, and PowerPoint- Good oral and written communication skills- Independent, self-starter with the desire to learn new skills and participate in continuous improvement projectsEducation:AssociateExperience:1-4 yearsQualifications:- Associate degree, Bachelors degree, or relevant experience- Minimum one year of similar or related experience in document control coordination, processing, or record retention role- Experience in quality assurance, with an understanding of quality system processes, preferred- Experience with ERP and electronic quality management system software such as SAP and EtQ software, preferred- High attention to detail Apply via the apply button in the top right hand corner today!Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      This position can be REMOTE!Spherion is recruiting a Quality Systems Project Associate! In this position, you will be an integral member of the team dedicated to assisting our client in maintaining compliance with key quality system processes.Responsibilities:- Support key day-to-day tasks within the supplier quality team, including supplier change notifications, supplier approvals, and direct material approvals- Perform project assignments to support the supplier quality organization- Modify and create procedures, forms, and records necessary for the quality system- Complete actions assigned from audits, deviations, changes, nonconformances, etc.- Assist in the creation of metrics applicable to review processes and report results and suggestions to management or other stakeholders- Represent the Quality System team in projects, as assigned- Work with QS and/or other process or business leaders on urgent/critical activities or corrective actions needed for the businessWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent organizational skills- Advanced PC skills to include proficiency in Word, Excel, SharePoint, Outlook, and PowerPoint- Good oral and written communication skills- Independent, self-starter with the desire to learn new skills and participate in continuous improvement projectsEducation:AssociateExperience:1-4 yearsQualifications:- Associate degree, Bachelors degree, or relevant experience- Minimum one year of similar or related experience in document control coordination, processing, or record retention role- Experience in quality assurance, with an understanding of quality system processes, preferred- Experience with ERP and electronic quality management system software such as SAP and EtQ software, preferred- High attention to detail Apply via the apply button in the top right hand corner today!Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Conroe, Texas
      • Temp to Perm
      • $17.00 - $18.00 per hour
      • 8:00 AM - 5:00 PM (Various Shifts Available)
      Spherion has partnered with a local Conroe company hiring for a Lab Technician position in the food industry. This position requires Lab experience in the food industry.Responsibilities:Perform microbiological, chemical, physical, and sensory analysis of product.Hold, release, and reject finished goods based on product analysis.Verify compliance and alert management of any deviations from specifications.Perform in-plant weight checks, temperature checks, ingredient usage and distribution, finished product appearance, code date verification, pH testing and metal detection verification.Perform calibration and scheduled preventative maintenance on lab equipment.Responsible for daily finished product evaluations.Perform environment testing.Maintain documentation on all tests performed in lab.Maintain a clean, sanitary, and safe work area.Working hours: 8:00 AM - 5:00 PM (Various Shifts Available)Skills:Capable of working in a fast-paced environmentCapable of performing repetitive tasksTeam-oriented and organizedComfortable working long shiftsEducation:High SchoolExperience:1-4 yearsQualifications:Must be able to frequently stand, walk, kneel, reach, climb, pull, and bend.Must be able to routinely lift and/or move up to 50 pounds; and occasionally 75 pounds.Must be able to work for extended periods in a cold, damp environment.Lab Technician position in the food industry. Must have Lab experience in the food industry. Call or Text "APPLY" to 936/207-1150Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion has partnered with a local Conroe company hiring for a Lab Technician position in the food industry. This position requires Lab experience in the food industry.Responsibilities:Perform microbiological, chemical, physical, and sensory analysis of product.Hold, release, and reject finished goods based on product analysis.Verify compliance and alert management of any deviations from specifications.Perform in-plant weight checks, temperature checks, ingredient usage and distribution, finished product appearance, code date verification, pH testing and metal detection verification.Perform calibration and scheduled preventative maintenance on lab equipment.Responsible for daily finished product evaluations.Perform environment testing.Maintain documentation on all tests performed in lab.Maintain a clean, sanitary, and safe work area.Working hours: 8:00 AM - 5:00 PM (Various Shifts Available)Skills:Capable of working in a fast-paced environmentCapable of performing repetitive tasksTeam-oriented and organizedComfortable working long shiftsEducation:High SchoolExperience:1-4 yearsQualifications:Must be able to frequently stand, walk, kneel, reach, climb, pull, and bend.Must be able to routinely lift and/or move up to 50 pounds; and occasionally 75 pounds.Must be able to work for extended periods in a cold, damp environment.Lab Technician position in the food industry. Must have Lab experience in the food industry. Call or Text "APPLY" to 936/207-1150Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • College Station, Texas
      • Permanent
      • $21.00 - $23.22 per hour
      • Various Shifts Available
      Spherion Staffing has partnered with FUJIFILM Diosynth Biotechnologies to recruit for this role. This is an exciting opportunity to be a part of the cutting-edge project of COVID-19 vaccine production. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department, working in various manufacturing operations such as vaccine and therapeutic production.Responsibilities:Opportunity to work with protein purification, various filtration systems, and cell cultivationOperation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records, training providedResponsible for learning and applying current Good Manufacturing PracticeWorking hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills.Ability to receive training in various filtration and analytical techniquesGood self-discipline and attention to detail.Must be able to work flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary.Must be able to work alternative shift hours and weekends as required.Possess effective time management and organizational skillsMust possess excellent math and computer skillsSafety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma/GED, with 1 year of relevant experience; ORAssociates degree in life sciences field with 0 ??? 1 years experience preferredExpress strong interest in a career preferably in Chemistry, Biology, Life Sciences or a related field.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:Experience prolonged standing, bending, stooping, twisting, and stretching.Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and glovesLift and/or move 25-50 pounds frequently.Attendance is mandatory.Additional working conditions & physical requirements for some positions:No makeup or jewelry can be worn when working in the clean room environment.Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply online today and a recruiter will reach out once your information has been reviewed, and schedule you for an interview.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with FUJIFILM Diosynth Biotechnologies to recruit for this role. This is an exciting opportunity to be a part of the cutting-edge project of COVID-19 vaccine production. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department, working in various manufacturing operations such as vaccine and therapeutic production.Responsibilities:Opportunity to work with protein purification, various filtration systems, and cell cultivationOperation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records, training providedResponsible for learning and applying current Good Manufacturing PracticeWorking hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills.Ability to receive training in various filtration and analytical techniquesGood self-discipline and attention to detail.Must be able to work flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary.Must be able to work alternative shift hours and weekends as required.Possess effective time management and organizational skillsMust possess excellent math and computer skillsSafety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma/GED, with 1 year of relevant experience; ORAssociates degree in life sciences field with 0 ??? 1 years experience preferredExpress strong interest in a career preferably in Chemistry, Biology, Life Sciences or a related field.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:Experience prolonged standing, bending, stooping, twisting, and stretching.Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and glovesLift and/or move 25-50 pounds frequently.Attendance is mandatory.Additional working conditions & physical requirements for some positions:No makeup or jewelry can be worn when working in the clean room environment.Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply online today and a recruiter will reach out once your information has been reviewed, and schedule you for an interview.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Madison, Wisconsin
      • Temp to Perm
      • $19.00 - $22.00 per hour
      • 6:00 AM - 4:30 PM
      Spherion is recruiting a Product Finishing Technician! This position is responsible for operating and maintaining our biotechnology clients dispensing, kitting, and labeling machinery. If you are detail-oriented and work well in a team-oriented environment, this position is for you!Responsibilities:- Setup, operate, and maintain manual and automated dispensing, capping, and labeling equipment- Pull products from inventory and assemble components into kits and kit sub-assemblies using quality system documents, including kit packaging diagrams (KPDs)- Accurately complete all required written documentation for batch records- Maintain and close shop orders in the clients ERP System- Address product non-conformity appropriately- Follow contamination prevention procedures- Understand and comply with ethical, legal, and regulatory requirements applicable to our clients business- Provide a high level of both intradepartmental and interdepartmental (Production, Marketing, Shipping, Materials Management) customer service as needed- Clean production areas and equipment as needed- Assist R&D in the dispensing of new products for validation prior to new product launch as neededWorking hours: 6:00 AM - 4:30 PMSkills:- Good organizational and prioritization skills- High level of attention to detailEducation:High SchoolExperience:1-4 yearsQualifications:- High school education or GED required- At least one year of science or laboratory background in a production environment with exposure to various production and packaging equipment preferred- Experience in a regulated production environment preferred- Disclosure of COVID-19 vaccination status- Ability to work quickly and accurately- Competency in general math- Computer experience in ERP Systems, word, excel, and outlookPhysical Requirements:- Ability to work in a cleanroom environment- Ability to use computer and telephone equipment- Manual dexterity to assemble kits and dispense product- Ability to stand and/or sit for several hours at a time- Ability to lift objects weighing up to 50-70 lbs. occasionally- Ability to move up to 300 lbs. on a dolly and 500 lbs. on a pallet jack occasionally- Ability to bend multiple times per day- Ability to use hands for repetitive motions throughout shift- Visual acuity for quality inspections- Ability to work in -20 degrees C temperature occasionally Apply via the apply button in the top right hand corner today!Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion is recruiting a Product Finishing Technician! This position is responsible for operating and maintaining our biotechnology clients dispensing, kitting, and labeling machinery. If you are detail-oriented and work well in a team-oriented environment, this position is for you!Responsibilities:- Setup, operate, and maintain manual and automated dispensing, capping, and labeling equipment- Pull products from inventory and assemble components into kits and kit sub-assemblies using quality system documents, including kit packaging diagrams (KPDs)- Accurately complete all required written documentation for batch records- Maintain and close shop orders in the clients ERP System- Address product non-conformity appropriately- Follow contamination prevention procedures- Understand and comply with ethical, legal, and regulatory requirements applicable to our clients business- Provide a high level of both intradepartmental and interdepartmental (Production, Marketing, Shipping, Materials Management) customer service as needed- Clean production areas and equipment as needed- Assist R&D in the dispensing of new products for validation prior to new product launch as neededWorking hours: 6:00 AM - 4:30 PMSkills:- Good organizational and prioritization skills- High level of attention to detailEducation:High SchoolExperience:1-4 yearsQualifications:- High school education or GED required- At least one year of science or laboratory background in a production environment with exposure to various production and packaging equipment preferred- Experience in a regulated production environment preferred- Disclosure of COVID-19 vaccination status- Ability to work quickly and accurately- Competency in general math- Computer experience in ERP Systems, word, excel, and outlookPhysical Requirements:- Ability to work in a cleanroom environment- Ability to use computer and telephone equipment- Manual dexterity to assemble kits and dispense product- Ability to stand and/or sit for several hours at a time- Ability to lift objects weighing up to 50-70 lbs. occasionally- Ability to move up to 300 lbs. on a dolly and 500 lbs. on a pallet jack occasionally- Ability to bend multiple times per day- Ability to use hands for repetitive motions throughout shift- Visual acuity for quality inspections- Ability to work in -20 degrees C temperature occasionally Apply via the apply button in the top right hand corner today!Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • College Station, Texas
      • Permanent
      • $19.00 - $23.00 per hour
      • Various Shifts Available
      Spherion Staffing has partnered with a growing dietary supplements manufacturing facility in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in the cGMP fermentation facility and work on the manufacture of proprietary microorganisms.Responsibilities:Responsibilities: Prepare production media and buffers, sterilize equipment, operate bioreactors, and perform seed scale-up from lab pilot to production scale.Assist with production equipment maintenance, including cleaning, preventative maintenance, and optimizationEnsure work is completed in compliance with all SOP???s, batch records, controlled documentation, and all applicable regulations, guidelines, safety policies and proceduresParticipate in cleaning and equipment validation efforts as well as validation documents within a cGMP facility.Author, review, and revise deviations/CAPA???s, manufacturing and process equipment documentation, and other technical documentation, as necessary.Operate and use all equipment and chemicals in a safe manner.Participate in cross-training initiatives and assist with training manufacturing associates when needed.Maintain accurate and timely record of equipment service records, and work collaboratively with various departments to compile, analyze, and interpret data.Manage the cycle count process, and ensure cycle counting of the warehouse inventory are accurate and on time.Ensure that the shipping schedule is correctly implemented and report any deviations to Customer Service.Operate in a sterile environment and ensure there is no cross contamination.Develop and maintain proper bacterial management practices to ensure consistent microbial cell culture that meet quality standards and keep pace with desired production goals.Working hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills. Good self-discipline and attention to detail.Must possess strong work ethic and prioritization skills. Must be able to work 12-hour shift and be willing to work outside of normal, scheduled hours; as necessary. Experience working in a cleanroom environment in full sterile room gowning and good aseptic technique. Possess effective time management and organizational skills Must possess excellent math and computer skills Safety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 0-1 years of relevant experience; OR High School Diploma or equivalency with 1-2 years of previous mechanical experience (vehicle shop, machine shop, fabrication shop)**Must possess a valid US Driver???s license Preferred:Previous fermentation experience (including centrifugation) strongly preferred.Previous experience maintaining large pieces of machinery Previous experience with liquid processing equipment (pumps, valves, mixers, heating, cooling, etc.)The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:?? Experience prolonged standing, bending, stooping, twisting, and stretching.?? Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.?? Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves?? Lift 60 lbs. Must be able to tolerate the noise and odor that results from microbial cell culture.?? Additional working conditions & physical requirements for some positions:?? No make-up or jewelry can be worn when working in the clean room environment.?? Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Work Hours:Must be able to work 12 hour shifts, 1st, 2nd, or 3rd shift Please apply online today! Once you have applied, you will receive a pre screen to complete, and then a recruiter will review your information and contact you to schedule an interview.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a growing dietary supplements manufacturing facility in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in the cGMP fermentation facility and work on the manufacture of proprietary microorganisms.Responsibilities:Responsibilities: Prepare production media and buffers, sterilize equipment, operate bioreactors, and perform seed scale-up from lab pilot to production scale.Assist with production equipment maintenance, including cleaning, preventative maintenance, and optimizationEnsure work is completed in compliance with all SOP???s, batch records, controlled documentation, and all applicable regulations, guidelines, safety policies and proceduresParticipate in cleaning and equipment validation efforts as well as validation documents within a cGMP facility.Author, review, and revise deviations/CAPA???s, manufacturing and process equipment documentation, and other technical documentation, as necessary.Operate and use all equipment and chemicals in a safe manner.Participate in cross-training initiatives and assist with training manufacturing associates when needed.Maintain accurate and timely record of equipment service records, and work collaboratively with various departments to compile, analyze, and interpret data.Manage the cycle count process, and ensure cycle counting of the warehouse inventory are accurate and on time.Ensure that the shipping schedule is correctly implemented and report any deviations to Customer Service.Operate in a sterile environment and ensure there is no cross contamination.Develop and maintain proper bacterial management practices to ensure consistent microbial cell culture that meet quality standards and keep pace with desired production goals.Working hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills. Good self-discipline and attention to detail.Must possess strong work ethic and prioritization skills. Must be able to work 12-hour shift and be willing to work outside of normal, scheduled hours; as necessary. Experience working in a cleanroom environment in full sterile room gowning and good aseptic technique. Possess effective time management and organizational skills Must possess excellent math and computer skills Safety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 0-1 years of relevant experience; OR High School Diploma or equivalency with 1-2 years of previous mechanical experience (vehicle shop, machine shop, fabrication shop)**Must possess a valid US Driver???s license Preferred:Previous fermentation experience (including centrifugation) strongly preferred.Previous experience maintaining large pieces of machinery Previous experience with liquid processing equipment (pumps, valves, mixers, heating, cooling, etc.)The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:?? Experience prolonged standing, bending, stooping, twisting, and stretching.?? Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.?? Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves?? Lift 60 lbs. Must be able to tolerate the noise and odor that results from microbial cell culture.?? Additional working conditions & physical requirements for some positions:?? No make-up or jewelry can be worn when working in the clean room environment.?? Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Work Hours:Must be able to work 12 hour shifts, 1st, 2nd, or 3rd shift Please apply online today! Once you have applied, you will receive a pre screen to complete, and then a recruiter will review your information and contact you to schedule an interview.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • College Station, Texas
      • Permanent
      • $25.00 - $37.00 per hour
      • Various Shifts Available
      Spherion Staffing has partnered with a leading biotechnology company in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department. This role will be responsible for working in various manufacturing operations such as vaccine and therapeutic production in accordance with GMP (good manufacturing practice) regulations.Responsibilities:Upstream manufacturing duties include: overseeing cell cultivation process, plate counting, microscopic examination, banking of cell lines and viruses, operating bacterial fermentation culture vessels, and operating bioreactors?? Downstream manufacturing duties include: overseeing filtration and purification processes by working with various filtration systems (e.g. Tangential Flow Filtration, nanofiltration and depth filtration), chromatographic systems, and aseptic process simulation and drug product filling?? Operation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.?? Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records according to cGMP regulations, and ensure other team members are trained.?? Perform lab maintenance duties by assisting with daily cleaning and sanitizing of sterile production areas.Working hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills.- Strong leadership skills and ability to provide training to others on cGMP regulations- Good self-discipline and attention to detail.- Must be able to work 12-hour shift and be willing to work outside of normal, scheduled hours; as necessary.- Experience working in a cleanroom environment in full sterile room gowning and good aseptic technique.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:AssociateExperience:1-4 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 2-4 years of relevant experience, with at least 1 year GMP experience;OR High School Diploma AND 3-6 years of relevant experience, with at least 2 years of GMP experience.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:?? Experience prolonged standing, bending, stooping, twisting, and stretching.?? Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.?? Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves?? Lift and/or move 25-50 pounds frequently.?? Attendance is mandatory.Additional working conditions & physical requirements for some positions:?? No make-up or jewelry can be worn when working in the clean room environment.?? Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply online today and a recruiter will reach out once your information has been reviewed, and schedule you for an interview.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your s
      Spherion Staffing has partnered with a leading biotechnology company in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department. This role will be responsible for working in various manufacturing operations such as vaccine and therapeutic production in accordance with GMP (good manufacturing practice) regulations.Responsibilities:Upstream manufacturing duties include: overseeing cell cultivation process, plate counting, microscopic examination, banking of cell lines and viruses, operating bacterial fermentation culture vessels, and operating bioreactors?? Downstream manufacturing duties include: overseeing filtration and purification processes by working with various filtration systems (e.g. Tangential Flow Filtration, nanofiltration and depth filtration), chromatographic systems, and aseptic process simulation and drug product filling?? Operation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.?? Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records according to cGMP regulations, and ensure other team members are trained.?? Perform lab maintenance duties by assisting with daily cleaning and sanitizing of sterile production areas.Working hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills.- Strong leadership skills and ability to provide training to others on cGMP regulations- Good self-discipline and attention to detail.- Must be able to work 12-hour shift and be willing to work outside of normal, scheduled hours; as necessary.- Experience working in a cleanroom environment in full sterile room gowning and good aseptic technique.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:AssociateExperience:1-4 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 2-4 years of relevant experience, with at least 1 year GMP experience;OR High School Diploma AND 3-6 years of relevant experience, with at least 2 years of GMP experience.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:?? Experience prolonged standing, bending, stooping, twisting, and stretching.?? Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.?? Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves?? Lift and/or move 25-50 pounds frequently.?? Attendance is mandatory.Additional working conditions & physical requirements for some positions:?? No make-up or jewelry can be worn when working in the clean room environment.?? Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply online today and a recruiter will reach out once your information has been reviewed, and schedule you for an interview.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your s
      • Decatur, Illinois
      • Temp to Perm
      • $17.00 per hour
      • Various Shifts Available
      We are looking for a qualified Lab Technician to undertake a variety of laboratory procedures of technical nature. You will be handling sensitive equipment to analyze samples or substances and conduct tests reporting findings to a laboratory manager.The ideal candidate will be well-trained to maintain safety conditions and will be passionate for doing work that makes things move forward.Responsibilities:- Prepares process and finished product samples- Performs analytical testing using instrumental, wet chemistry procedures, and record results using computerized data systems- Performs daily process monitoring tests throughout the plant as assigned- Maintains samples of tested product in order to confirm test results, if necessary- Documents results of all testing procedures and promptly notifies operations of required adjustments- Enter and report data using a Laboratory Information Management Systems (LIMS).Understands most production processes required in the production of product and may make recommendations to operators in order to achieve product quality- Performs light maintenance and calibration on all ADM laboratory equipment- Maintains on-going records of the results of all testing procedures and inputs such data into computer on a daily basis- Maintains adequate supplies used for testing procedures and notifies the supervisor of the need to re-order such supplies- Continually compares equipment readouts with samples of standards as required to insure that all systems are operating accurately- Maintains a neat and clean working area at all times, washing equipment as required and placing equipment in the proper storage areas- Maintains an effective working relationship with fellow employees- Performs duties in a safe manner, utilizing all approved safety equipment and successfully completes all safety certification requirements- Maintains awareness and adheres to all FDA, GMP, BATF, EPA, OSHA and employer standards and guidelinesWorking hours: Various Shifts AvailableSkills:- Demonstrates sufficient computer skills to utilize lab instrument operation programs- Familiarity with current commercial software applications (Excel, Word)- Experience with lab documentation- Experience with operating standard lab equipment (i.e., pH meter, balances and spectrophotometer)- Demonstrates sufficient math skills to perform calculations associated with lab testing- Ability to work on multiple tasks- Ability to team build- Good organizational skills- Willingness to assume and learn new responsibilities- Excellent communication skills- Proven housekeeping and sanitation skills- Demonstrated troubleshooting skills- Accurate record keeping skills- Attendance and punctuality- Ability to lift up to 40 lbs- Ability to be on your feet for extended periods of time.Education:BachelorsExperience:1-4 yearsQualifications:- Education/Training Preferred: 2 or more years science degree. - Experience Preferred- Good attendance history- Excellent safety record and awareness- Previous plant experience Apply today at: https://www.spherion.com/apply/75103/Spherion thinks you deserve more cash this holiday season, so we're giving away thousands in our Spherion Get More! Giveaway. Each week you work for us* between Oct. 18 - Dec. 1, you get a digital scratchcard with aSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      We are looking for a qualified Lab Technician to undertake a variety of laboratory procedures of technical nature. You will be handling sensitive equipment to analyze samples or substances and conduct tests reporting findings to a laboratory manager.The ideal candidate will be well-trained to maintain safety conditions and will be passionate for doing work that makes things move forward.Responsibilities:- Prepares process and finished product samples- Performs analytical testing using instrumental, wet chemistry procedures, and record results using computerized data systems- Performs daily process monitoring tests throughout the plant as assigned- Maintains samples of tested product in order to confirm test results, if necessary- Documents results of all testing procedures and promptly notifies operations of required adjustments- Enter and report data using a Laboratory Information Management Systems (LIMS).Understands most production processes required in the production of product and may make recommendations to operators in order to achieve product quality- Performs light maintenance and calibration on all ADM laboratory equipment- Maintains on-going records of the results of all testing procedures and inputs such data into computer on a daily basis- Maintains adequate supplies used for testing procedures and notifies the supervisor of the need to re-order such supplies- Continually compares equipment readouts with samples of standards as required to insure that all systems are operating accurately- Maintains a neat and clean working area at all times, washing equipment as required and placing equipment in the proper storage areas- Maintains an effective working relationship with fellow employees- Performs duties in a safe manner, utilizing all approved safety equipment and successfully completes all safety certification requirements- Maintains awareness and adheres to all FDA, GMP, BATF, EPA, OSHA and employer standards and guidelinesWorking hours: Various Shifts AvailableSkills:- Demonstrates sufficient computer skills to utilize lab instrument operation programs- Familiarity with current commercial software applications (Excel, Word)- Experience with lab documentation- Experience with operating standard lab equipment (i.e., pH meter, balances and spectrophotometer)- Demonstrates sufficient math skills to perform calculations associated with lab testing- Ability to work on multiple tasks- Ability to team build- Good organizational skills- Willingness to assume and learn new responsibilities- Excellent communication skills- Proven housekeeping and sanitation skills- Demonstrated troubleshooting skills- Accurate record keeping skills- Attendance and punctuality- Ability to lift up to 40 lbs- Ability to be on your feet for extended periods of time.Education:BachelorsExperience:1-4 yearsQualifications:- Education/Training Preferred: 2 or more years science degree. - Experience Preferred- Good attendance history- Excellent safety record and awareness- Previous plant experience Apply today at: https://www.spherion.com/apply/75103/Spherion thinks you deserve more cash this holiday season, so we're giving away thousands in our Spherion Get More! Giveaway. Each week you work for us* between Oct. 18 - Dec. 1, you get a digital scratchcard with aSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

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