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      • Spring, Texas
      • Temp to Perm
      • $25.00 - $29.00 per hour
      • 6:00 AM - 3:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:* Oversee employees in the manufacturing department, including task delegation.* Assist in scaling-up processes.* Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines.* Ensure team is manufacturing plasmid DNA in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.* Execute validation protocols as needed.* Write Standard Operating Procedures.* Install, document, and maintain equipment as needed.Working hours: 6:00 AM - 3:00 PMSkills:* Possess leadership skills.* Excellent written and oral communication skills.* Ability to work in a clean room environment for extended periods of time.* Ability to wear and work in PPE.Education:BachelorsExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a science related field with 3 or more years of cGMP manufacturing experience.* Plasmid purification experience, preferred.* Knowledge of microbiological techniques, preferred. www.spherion.com/applySpherion 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 bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:* Oversee employees in the manufacturing department, including task delegation.* Assist in scaling-up processes.* Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines.* Ensure team is manufacturing plasmid DNA in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.* Execute validation protocols as needed.* Write Standard Operating Procedures.* Install, document, and maintain equipment as needed.Working hours: 6:00 AM - 3:00 PMSkills:* Possess leadership skills.* Excellent written and oral communication skills.* Ability to work in a clean room environment for extended periods of time.* Ability to wear and work in PPE.Education:BachelorsExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a science related field with 3 or more years of cGMP manufacturing experience.* Plasmid purification experience, preferred.* Knowledge of microbiological techniques, preferred. www.spherion.com/applySpherion 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.
      • Spring, Texas
      • Temp to Perm
      • $19.00 - $20.00 per hour
      • 12:00 AM - 12:00 AM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:* Review and verify all manufacturing batch documentation, production records, and ensure the documentation complies with regulations and internal quality control practices.* Assist in reviewing and writing Standard Operating Procedures for manufacturing, and protocols for development, Installation Qualification (IQ) and Operational Qualification (OQ) and validations.* Assist in routine internal audits, review deviations and investigations.* Ensure compliance with Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's).Working hours: 12:00 AM - 12:00 AMSkills:* Excellent written and oral communication skills.* Meticulous organizational skills and demonstrating meticulous documentation and record review practices.* Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:* Associate's degree and/or one to three years of relevant experience.* Must have previous technical/ scientific writing experience.* Experience working in a GMP facility or pharmaceutical environment is preferred.* Experience with microbiology techniques is preferred. www.spherion.com/applySpherion 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 bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:* Review and verify all manufacturing batch documentation, production records, and ensure the documentation complies with regulations and internal quality control practices.* Assist in reviewing and writing Standard Operating Procedures for manufacturing, and protocols for development, Installation Qualification (IQ) and Operational Qualification (OQ) and validations.* Assist in routine internal audits, review deviations and investigations.* Ensure compliance with Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's).Working hours: 12:00 AM - 12:00 AMSkills:* Excellent written and oral communication skills.* Meticulous organizational skills and demonstrating meticulous documentation and record review practices.* Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:* Associate's degree and/or one to three years of relevant experience.* Must have previous technical/ scientific writing experience.* Experience working in a GMP facility or pharmaceutical environment is preferred.* Experience with microbiology techniques is preferred. www.spherion.com/applySpherion 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.
      • Spring, Texas
      • Temp to Perm
      • $17.00 - $18.00 per hour
      • 6:00 AM - 3:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure purity of research and GMP materials.Responsibilities:* Maintain, clean, and sterilize manufacturing equipment.* Perform preventative maintenance.* Document activities as required for GMP materials.* Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:* Organization.* Attention to detail.* Scientific documentation.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma or general education degree (GED); or one to three months related experience and/or training.Experience working in a GMP facility or pharmaceutical environment is preferred. Apply today at www.spherion.com/applySpherion 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 bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure purity of research and GMP materials.Responsibilities:* Maintain, clean, and sterilize manufacturing equipment.* Perform preventative maintenance.* Document activities as required for GMP materials.* Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:* Organization.* Attention to detail.* Scientific documentation.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma or general education degree (GED); or one to three months related experience and/or training.Experience working in a GMP facility or pharmaceutical environment is preferred. Apply today at www.spherion.com/applySpherion 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.
      • Spring, Texas
      • Temp to Perm
      • $19.00 - $20.00 per hour
      • 8:00 AM - 5:00 AM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:*Review all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. www.spherion.com/applySpherion 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 bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:*Review all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. www.spherion.com/applySpherion 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.
      • Bryan, Texas
      • Permanent
      • $19.00 - $23.00 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 related field. Please apply online today and a recruiter will contact you to conduct a pre-screen!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 related field. Please apply online today and a recruiter will contact you to conduct a pre-screen!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.
      • Bryan, 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.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. Apply online today and a recruiter will review your information and reach out 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, Relig
      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.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. Apply online today and a recruiter will review your information and reach out 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, Relig
      • Raleigh, North Carolina
      • Permanent
      • $19.00 - $25.00 per hour
      • Various Shifts Available
      Great opportunity to join a fast growing biotech in the Triangle!The Packaging Operator is responsible for inspecting and packaging of terminally sterilized and aseptically produced pharmaceutical drugs in accordance with current Good Manufacturing Practices.Great pay, benefits and culture!Responsibilities:- 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-lineprojects.- Other duties as assigned with or without accommodation.Working hours: Various Shifts AvailableSkills:- Good verbal and written communication skills- Ability to work both on a team and individually- Operator must understand and adhere to standard operating procedures 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 quality of product.- Responsible for monitoring the process and documenting measurements per SOP.- Responsible for compliance with FDA, OSHA, cGMP- 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- Ability to lift 50 pounds- Good math and reading skills- Mental and visual acuity for production of and identification of quality productEducation:High SchoolExperience:1-4 yearsQualifications:- High School diploma, GED, or equivalent- 1-3 years pharmaceutical manufacturing experience within a sterile environment (i.e. ISO 5E or similar) Apply online today, send your resume to haleynicol@spherion.com or call 919-873-5588Spherion 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.
      Great opportunity to join a fast growing biotech in the Triangle!The Packaging Operator is responsible for inspecting and packaging of terminally sterilized and aseptically produced pharmaceutical drugs in accordance with current Good Manufacturing Practices.Great pay, benefits and culture!Responsibilities:- 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-lineprojects.- Other duties as assigned with or without accommodation.Working hours: Various Shifts AvailableSkills:- Good verbal and written communication skills- Ability to work both on a team and individually- Operator must understand and adhere to standard operating procedures 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 quality of product.- Responsible for monitoring the process and documenting measurements per SOP.- Responsible for compliance with FDA, OSHA, cGMP- 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- Ability to lift 50 pounds- Good math and reading skills- Mental and visual acuity for production of and identification of quality productEducation:High SchoolExperience:1-4 yearsQualifications:- High School diploma, GED, or equivalent- 1-3 years pharmaceutical manufacturing experience within a sterile environment (i.e. ISO 5E or similar) Apply online today, send your resume to haleynicol@spherion.com or call 919-873-5588Spherion 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
      • Permanent
      • $19.00 - $25.00 per hour
      • Various Shifts Available
      Fast growing biotech in Raleigh is looking for experienced Setup Operators! The Production Filling Setup Operator will prepare the equipment prior to the start of each batch operation in accordance with all SOP's and quality controls applicable to that operation, making adjustments for size and/or product as necessary.Great pay, benefits and work environment - Apply now!Responsibilities:- Assemble, disassemble, maintain, and sanitize the production operating equipment as necessary.- Processing components (washing, extracting, rinsing, and siliconizing)- Monitor production equipment while in operation to ensure quality of product.- Ensure that production equipment is safe and that while in operation it is run safely by all personnel.- Complete all necessary documentation regarding the equipment and its operational performance to meet regulatory and cGMP requirements.- Operate an autoclave to sterilize product prior to packaging.- Operate in an ISO5 or lower classified area- 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.- Assist Team Leader in coordinating maintenance activities.- Prevent excess waste of product and/or components by operating the equipment in an efficient manner.- Maintain production schedules.- Work with groups in initiating and implementation of programs such as continuous improvement (Lean) and autonomous maintenance (TPM).- Other duties as assigned with or without accommodation.Working hours: Various Shifts AvailableSkills:- Good verbal and interpersonal communication skills- Basic knowledge and use of hand tools- Sound decision making skills- Good math, reading, writing skills- Demonstrated mechanical aptitude- Mental and visual acuity for production of quality product- Strong trouble shooting skills- Basic computer skills - Microsoft Office package- Ability to lift up to 50 poundsEducation:High SchoolExperience:1-4 yearsQualifications:- High School diploma, GED, or equivalent required- 2 year Technical degree preferred- 2-5 years experience as a Production Set-up Operator or mechanic in a pharmaceutical manufacturing environment (preferred). If you have biotech experience we are looking for you! Apply online today, send your resume to haleynicol@spherion.com or call 919-873-5588Spherion 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.
      Fast growing biotech in Raleigh is looking for experienced Setup Operators! The Production Filling Setup Operator will prepare the equipment prior to the start of each batch operation in accordance with all SOP's and quality controls applicable to that operation, making adjustments for size and/or product as necessary.Great pay, benefits and work environment - Apply now!Responsibilities:- Assemble, disassemble, maintain, and sanitize the production operating equipment as necessary.- Processing components (washing, extracting, rinsing, and siliconizing)- Monitor production equipment while in operation to ensure quality of product.- Ensure that production equipment is safe and that while in operation it is run safely by all personnel.- Complete all necessary documentation regarding the equipment and its operational performance to meet regulatory and cGMP requirements.- Operate an autoclave to sterilize product prior to packaging.- Operate in an ISO5 or lower classified area- 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.- Assist Team Leader in coordinating maintenance activities.- Prevent excess waste of product and/or components by operating the equipment in an efficient manner.- Maintain production schedules.- Work with groups in initiating and implementation of programs such as continuous improvement (Lean) and autonomous maintenance (TPM).- Other duties as assigned with or without accommodation.Working hours: Various Shifts AvailableSkills:- Good verbal and interpersonal communication skills- Basic knowledge and use of hand tools- Sound decision making skills- Good math, reading, writing skills- Demonstrated mechanical aptitude- Mental and visual acuity for production of quality product- Strong trouble shooting skills- Basic computer skills - Microsoft Office package- Ability to lift up to 50 poundsEducation:High SchoolExperience:1-4 yearsQualifications:- High School diploma, GED, or equivalent required- 2 year Technical degree preferred- 2-5 years experience as a Production Set-up Operator or mechanic in a pharmaceutical manufacturing environment (preferred). If you have biotech experience we are looking for you! Apply online today, send your resume to haleynicol@spherion.com or call 919-873-5588Spherion 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
      • Permanent
      • $60,000 - $90,000 per year
      • 7:00 AM - 3:30 PM
      Spherion, in partnership with our Madison, WI-based biotechnology client, is recruiting for a Metrologist! This position ensures equipment used in the design, manufacture, and quality control testing of client products is calibrated in alignment with industry standards. You will be responsible for maintenance, testing, troubleshooting, and calibration on a variety of analytical equipment and instrumentation for laboratory and manufacturing applications among other duties.This is a direct-hire position!Responsibilities:- Serve as a departmental Subject Matter Expert in Metrology Science as it applies to analytical and manufacturing equipment typical of the clients business- Contribute to the development and improvement of departmental Standard Operating Procedures to ensure compliance and effectiveness of the clients calibration program- Perform calibration, repair, and preventive maintenance of laboratory and manufacturing equipment- Perform Metrology planner activities, including the creation of equipment, creation of maintenance plans, monitoring and assigning work orders, approving, and making usage decisions, and closing Metrology repair work orders- Perform support activities for Metrology materials, including monitoring spare parts, ordering stock spare parts, inventorying parts as required, and maintenance of the spare parts inventory- Work closely with department leadership and stay informed of all department-related activities- Work in a positive team environment and participate in department projects, with effective problem resolution- Make decisions in daily tasks that focus on the best interests of the workgroup, department, and company- Work under moderate supervision and complete tasks as assigned, with frequent changes to priorities- Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity, and respect for others- Embracing and being open to incorporating the client's 6 Emotional & Social Intelligence (ESI) core principles in daily work- Understand and comply with ethical, legal, and regulatory requirements applicable to the client's businessWorking hours: 7:00 AM - 3:30 PMSkills:- Ability to work and communicate well with a diversified scientific staff and respond promptly and efficiently to their needs- Ability to prioritize work activities in a manner that results in efficient and responsive department performance- Ability to maintain a positive, productive, and flexible work attitude with a willingness to adjust their schedule as required- Ability to move objects ranging in weight up to 60 lbs., up to 1 hour per day- Ability to work at a computer for extended periods of time- Ability to work in areas with limited space- Ability to climb ladders occasionally- Ability to work in a cleanroom environment- Ability to stand and/or sit for several hours at a time- Ability to bend multiple times per day- Ability to use hands for repetitive motions throughout shift- Ability to move in and out of environments up to -20 degrees C temperature occasionally- Ability to use a computer/Microsoft Office applicationsEducation:High SchoolExperience:1-4 yearsQualifications:- High School Diploma or equivalent required- Between three and six years of laboratory instrument calibration experience, or equivalent- Working knowledge of Microsoft Office, especially Excel- Advanced knowledge of Metrology, such as information regarding equipment, parts, calibration schedules, manuals, and work orders can be processed and understood. A degree in scientific/electronic/metrology discipline or equivalent- Minimum of 5 years of instrument maintenance and calibration experience- Experience in the use of computer software for ca
      Spherion, in partnership with our Madison, WI-based biotechnology client, is recruiting for a Metrologist! This position ensures equipment used in the design, manufacture, and quality control testing of client products is calibrated in alignment with industry standards. You will be responsible for maintenance, testing, troubleshooting, and calibration on a variety of analytical equipment and instrumentation for laboratory and manufacturing applications among other duties.This is a direct-hire position!Responsibilities:- Serve as a departmental Subject Matter Expert in Metrology Science as it applies to analytical and manufacturing equipment typical of the clients business- Contribute to the development and improvement of departmental Standard Operating Procedures to ensure compliance and effectiveness of the clients calibration program- Perform calibration, repair, and preventive maintenance of laboratory and manufacturing equipment- Perform Metrology planner activities, including the creation of equipment, creation of maintenance plans, monitoring and assigning work orders, approving, and making usage decisions, and closing Metrology repair work orders- Perform support activities for Metrology materials, including monitoring spare parts, ordering stock spare parts, inventorying parts as required, and maintenance of the spare parts inventory- Work closely with department leadership and stay informed of all department-related activities- Work in a positive team environment and participate in department projects, with effective problem resolution- Make decisions in daily tasks that focus on the best interests of the workgroup, department, and company- Work under moderate supervision and complete tasks as assigned, with frequent changes to priorities- Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity, and respect for others- Embracing and being open to incorporating the client's 6 Emotional & Social Intelligence (ESI) core principles in daily work- Understand and comply with ethical, legal, and regulatory requirements applicable to the client's businessWorking hours: 7:00 AM - 3:30 PMSkills:- Ability to work and communicate well with a diversified scientific staff and respond promptly and efficiently to their needs- Ability to prioritize work activities in a manner that results in efficient and responsive department performance- Ability to maintain a positive, productive, and flexible work attitude with a willingness to adjust their schedule as required- Ability to move objects ranging in weight up to 60 lbs., up to 1 hour per day- Ability to work at a computer for extended periods of time- Ability to work in areas with limited space- Ability to climb ladders occasionally- Ability to work in a cleanroom environment- Ability to stand and/or sit for several hours at a time- Ability to bend multiple times per day- Ability to use hands for repetitive motions throughout shift- Ability to move in and out of environments up to -20 degrees C temperature occasionally- Ability to use a computer/Microsoft Office applicationsEducation:High SchoolExperience:1-4 yearsQualifications:- High School Diploma or equivalent required- Between three and six years of laboratory instrument calibration experience, or equivalent- Working knowledge of Microsoft Office, especially Excel- Advanced knowledge of Metrology, such as information regarding equipment, parts, calibration schedules, manuals, and work orders can be processed and understood. A degree in scientific/electronic/metrology discipline or equivalent- Minimum of 5 years of instrument maintenance and calibration experience- Experience in the use of computer software for ca
      • Madison, Wisconsin
      • Permanent
      • $17.96 per hour
      • 8:00 AM - 5:00 PM
      Spherion, in partnership with our Madison, WI, based biotechnology client, is recruiting for an Operations Support Technician. This position will provide quality labware and staging preparation services to all IVD Manufacturing and Product Finishing Departments. This is a great, direct-hire opportunity for someone who is efficient with excellent attention to detail!Responsibilities:- Operate labware wash machines and autoclaves according to departmental operation and safety guidelines- Plan and maintain stock room supplies, stock all items used in the area of responsibility- Stage raw materials according to process orders -Maintain accurate daily activity logs and batch records- Keep work areas clean and free from clutter- Identify needs or problems and communicate proper courses of action on various cleaning issues and follow through to assure completion- Operate pH meters, conductivity meters, balances, autoclaves, peristaltic pumps, vacuum pumps, filtering apparatus, and laboratory mixing equipment- Plan daily schedule according to incoming requests- Identify unsafe situations, processes, or procedures and report them as appropriate- Meet customers needs in a professional manner- Understand and comply with ethical, legal, and regulatory requirements applicable to our clients business- Process Special Request from IVD Production, IVD Product Finishing and/or Engineering staff as needed- Assist in compiling information and data for special reports and assist with special projects as needed- Assist with training of others in the proper and safe use of all equipment as neededWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent communication skills- Strong attention to detailPhysical Requirements:- Standing, walking, and bending on a continuous basis as well as going up and down stairs- Ability to work in limited space areas- Ability to operate washing and drying labware equipment- Ability to move up to 300 lbs. on a dolly and 500 lbs. on a pallet jack occasionally- Ability to safely handle and transport glassware and labware items up to 300 liters in size and weighing up to 50 pounds for several hours per weekEducation:High SchoolExperience:1-4 yearsQualifications:- High School diploma or GED required, knowledge and/or coursework in biological sciences or chemistry preferred- Punctuality and ability to maintain a good attendance record are essential- Demonstrate a continuous willingness to be flexible with regard to job activities and associated scheduling- Maintenance of clean production areas and equipment- Competency in general math- The ability to work independently with moderate supervision and with other team members- Ability to use in-house software (Microsoft Office and ERP) to perform general duties- Ability to maintain a positive attitude toward work activities and show a willingness to accept direction and advice and be a team player- Previous work experience in glassware preparation within a laboratory setting preferred, but not required- A self-directed individual to work efficiently & accurately with strong customer service 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, in partnership with our Madison, WI, based biotechnology client, is recruiting for an Operations Support Technician. This position will provide quality labware and staging preparation services to all IVD Manufacturing and Product Finishing Departments. This is a great, direct-hire opportunity for someone who is efficient with excellent attention to detail!Responsibilities:- Operate labware wash machines and autoclaves according to departmental operation and safety guidelines- Plan and maintain stock room supplies, stock all items used in the area of responsibility- Stage raw materials according to process orders -Maintain accurate daily activity logs and batch records- Keep work areas clean and free from clutter- Identify needs or problems and communicate proper courses of action on various cleaning issues and follow through to assure completion- Operate pH meters, conductivity meters, balances, autoclaves, peristaltic pumps, vacuum pumps, filtering apparatus, and laboratory mixing equipment- Plan daily schedule according to incoming requests- Identify unsafe situations, processes, or procedures and report them as appropriate- Meet customers needs in a professional manner- Understand and comply with ethical, legal, and regulatory requirements applicable to our clients business- Process Special Request from IVD Production, IVD Product Finishing and/or Engineering staff as needed- Assist in compiling information and data for special reports and assist with special projects as needed- Assist with training of others in the proper and safe use of all equipment as neededWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent communication skills- Strong attention to detailPhysical Requirements:- Standing, walking, and bending on a continuous basis as well as going up and down stairs- Ability to work in limited space areas- Ability to operate washing and drying labware equipment- Ability to move up to 300 lbs. on a dolly and 500 lbs. on a pallet jack occasionally- Ability to safely handle and transport glassware and labware items up to 300 liters in size and weighing up to 50 pounds for several hours per weekEducation:High SchoolExperience:1-4 yearsQualifications:- High School diploma or GED required, knowledge and/or coursework in biological sciences or chemistry preferred- Punctuality and ability to maintain a good attendance record are essential- Demonstrate a continuous willingness to be flexible with regard to job activities and associated scheduling- Maintenance of clean production areas and equipment- Competency in general math- The ability to work independently with moderate supervision and with other team members- Ability to use in-house software (Microsoft Office and ERP) to perform general duties- Ability to maintain a positive attitude toward work activities and show a willingness to accept direction and advice and be a team player- Previous work experience in glassware preparation within a laboratory setting preferred, but not required- A self-directed individual to work efficiently & accurately with strong customer service 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.

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