You are successfully logged out of your my randstad account

You have successfully deleted your account

    Thank you for subscribing to your personalized job alerts.

    9 jobs found for Lab in Texas - Page 1

    Filter3
    Clear all
      • Spring, Texas
      • Temp to Perm
      • $18.00 - $20.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. Responsible for the maintenance, cleaning, and sterilization of equipment, supplies, and production areas.Responsibilities:* Wash glassware, plastic supplies, and other supporting equipment in a washer or by hand,as needed.* Sterilize materials to support PD/HD manufacture, testing and research.* Weekly and daily cleaning and disinfection of the PD production areas,including documentation of cleaning performed.* Restock main supplies in Production Areas*Perform basic in-process yield analysis of PD and MFG samples, including Miniprep andGel ElectrophoresisWorking hours: 8:00 AM - 5:00 PMSkills:*Lab maintenance and care*Clean room experienceEducation:High SchoolExperience:0-1 yearsQualifications:*1-3 Months related experience or training*Life Sciences background 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. Responsible for the maintenance, cleaning, and sterilization of equipment, supplies, and production areas.Responsibilities:* Wash glassware, plastic supplies, and other supporting equipment in a washer or by hand,as needed.* Sterilize materials to support PD/HD manufacture, testing and research.* Weekly and daily cleaning and disinfection of the PD production areas,including documentation of cleaning performed.* Restock main supplies in Production Areas*Perform basic in-process yield analysis of PD and MFG samples, including Miniprep andGel ElectrophoresisWorking hours: 8:00 AM - 5:00 PMSkills:*Lab maintenance and care*Clean room experienceEducation:High SchoolExperience:0-1 yearsQualifications:*1-3 Months related experience or training*Life Sciences background 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.
      • Dalhart, Texas
      • Temp to Perm
      • $15.00 per hour
      • 5:00 PM - 5:00 AM
      Responsible for accurate performance of all microbiological testing and sampling in the plant. Make sure to have timely and correct flow of information to facility staff and maintain customer service by filing and entering results into computer. Be able to transcribe results and initiate endpoint testing as needed. Keep up the ledgers and equipment to validate all processes performed. Other duties as assigned.Responsibilities:Perform lab tests presently conducted, and initiate lab testing in future; Report and enter results into computer and generate reporting data, manage and maintain confidential information, other duties as assignedRotating weekend shiftsWorking hours: 5:00 PM - 5:00 AMSkills:Ability to take initiativeAbility to multi-taskAble to follow instructionsAttention to DetailWritten & oral communicationAbility to read, write and speak EnglishAble to lift up to 45 Ibs.Education:High SchoolExperience:0-1 yearsQualifications:4 months or greater with experience in a lab settingHS Diploma/GEDBachelor Degree in Biology, Microbiology or related field is a plus but not requiredIntermediate experience with SAP and SharePoint systems a plus Submit your resume for consideration.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.
      Responsible for accurate performance of all microbiological testing and sampling in the plant. Make sure to have timely and correct flow of information to facility staff and maintain customer service by filing and entering results into computer. Be able to transcribe results and initiate endpoint testing as needed. Keep up the ledgers and equipment to validate all processes performed. Other duties as assigned.Responsibilities:Perform lab tests presently conducted, and initiate lab testing in future; Report and enter results into computer and generate reporting data, manage and maintain confidential information, other duties as assignedRotating weekend shiftsWorking hours: 5:00 PM - 5:00 AMSkills:Ability to take initiativeAbility to multi-taskAble to follow instructionsAttention to DetailWritten & oral communicationAbility to read, write and speak EnglishAble to lift up to 45 Ibs.Education:High SchoolExperience:0-1 yearsQualifications:4 months or greater with experience in a lab settingHS Diploma/GEDBachelor Degree in Biology, Microbiology or related field is a plus but not requiredIntermediate experience with SAP and SharePoint systems a plus Submit your resume for consideration.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.
      • 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.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:*Organization*Attention to detail*DocumentationEducation: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 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.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:*Organization*Attention to detail*DocumentationEducation: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 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.
      • Dalhart, Texas
      • Temp to Perm
      • $15.00 per hour
      • 11:00 PM - 11:00 AM
      Dalhart Texas-Complete daily MS cleaning schedule for lab, instruments, and utensils. Ensure prompt transmission of accurate data and information to the Plant and Food Safety Staff regarding trends, concerns and plant observations, conduct audits and spot checks as assigned, work independently with minimal supervision, help coach and train teammates and participate in on the job training, report any safety issues, observations or concerns,, other duties as assigned.Responsibilities:Participate in departmental safety teams, hold self and others accountable to food safety and sanitation guidelines and policies by communicating any food safety incidents, Ensure CLEAN reports oversee environmental disruption report and food safety permits through closureWorking hours: 11:00 PM - 11:00 AMSkills:Work well with othersAbility to follow detailed instructionsEffectively communicateMulti-task and organize prioritiesCritical thinking skills preferredMaintain confidentialityEducation:High SchoolExperience:0-1 yearsQualifications:Written and oral skillsHS Diploma/GEDMust be able to work weekends, holidays and rotating shiftsMust be able to pass pre-employment skills assessment4 months experience in lab/quality assurance or food safetyAbility to lift 45 lbsPast the level 1 post offer employment testing For consideration, please submit resume or come into the office to apply.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.
      Dalhart Texas-Complete daily MS cleaning schedule for lab, instruments, and utensils. Ensure prompt transmission of accurate data and information to the Plant and Food Safety Staff regarding trends, concerns and plant observations, conduct audits and spot checks as assigned, work independently with minimal supervision, help coach and train teammates and participate in on the job training, report any safety issues, observations or concerns,, other duties as assigned.Responsibilities:Participate in departmental safety teams, hold self and others accountable to food safety and sanitation guidelines and policies by communicating any food safety incidents, Ensure CLEAN reports oversee environmental disruption report and food safety permits through closureWorking hours: 11:00 PM - 11:00 AMSkills:Work well with othersAbility to follow detailed instructionsEffectively communicateMulti-task and organize prioritiesCritical thinking skills preferredMaintain confidentialityEducation:High SchoolExperience:0-1 yearsQualifications:Written and oral skillsHS Diploma/GEDMust be able to work weekends, holidays and rotating shiftsMust be able to pass pre-employment skills assessment4 months experience in lab/quality assurance or food safetyAbility to lift 45 lbsPast the level 1 post offer employment testing For consideration, please submit resume or come into the office to apply.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.
      • 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.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*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:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques 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.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*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:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques 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
      • $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
      • Spring, Texas
      • Temp to Perm
      • $20.00 - $23.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to review documentation of the Process Development team to ensure compliance with regulatory requirements.Responsibilities:* Review for compliance and approve all documentation for Research Grade and Highly Documented products.* Write up deviations and investigations.* Write and review all SOPs for Process Development team.* Review records related to production and process development. * Follow GMPs and SOPs to ensure company compliance. * Maintain applicable product inventories.* Summarize data.* Write Plasmid DNA evaluation summaries.Working hours: 8:00 AM - 5:00 PMSkills:* Must have previous technical writing experience in a lab setting.* Experience working in a GMP facility or pharmaceutical environment.* Experience with GMPs and SOPs as applicable to manufacture of Plasmid DNA* Technical writing and reviewing abilities. * Attention to detail and commitment to compliance.* Ability to identify and document scientific deviations.* Inventory maintenance.Education:AssociateExperience:1-4 yearsQualifications:* Associates degree.* Between 1 - 3 years experience in related role. 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 review documentation of the Process Development team to ensure compliance with regulatory requirements.Responsibilities:* Review for compliance and approve all documentation for Research Grade and Highly Documented products.* Write up deviations and investigations.* Write and review all SOPs for Process Development team.* Review records related to production and process development. * Follow GMPs and SOPs to ensure company compliance. * Maintain applicable product inventories.* Summarize data.* Write Plasmid DNA evaluation summaries.Working hours: 8:00 AM - 5:00 PMSkills:* Must have previous technical writing experience in a lab setting.* Experience working in a GMP facility or pharmaceutical environment.* Experience with GMPs and SOPs as applicable to manufacture of Plasmid DNA* Technical writing and reviewing abilities. * Attention to detail and commitment to compliance.* Ability to identify and document scientific deviations.* Inventory maintenance.Education:AssociateExperience:1-4 yearsQualifications:* Associates degree.* Between 1 - 3 years experience in related role. 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.
      • Wichita Falls, Texas
      • Temp to Perm
      • $17.00 - $21.00 per hour
      • 5:00 AM - 3:30 PM
      Spherion is searching for a Chemist to join a great manufacturing team here in Wichita Falls!Responsibilities:Quide Quality Control technician in testing of daily production batches and reviewing daily batch sheetsUpkeep and calibration of all lab instruments and suppliesTesting and qualification of raw materialsMaintain logs for all batches testedWork closely with all production supervisors to address any OOS batchesMethod development to test stability, performance, and quality of new and existing productsEstablish, modify, and create SOPs current and new test methodsUndertake special projects to formulate new products for customers. Maintain records to keep track of the development of new products and retention of all physical samplesRequires and extensive Chemistry background to understand the composition of active materials that will be used in the formulation of special productsWorking hours: 5:00 AM - 3:30 PMSkills:Extensive background in Chemistry, pay will depend on experience and educationExtreme attention to detailOrganization skills are a mustKnowledge of general safety practicesEducation:BachelorsExperience:1-4 yearsQualifications:High school diploma or equivalent requiredMust submit to background check and drug screen Please register at www.spherion.com/apply. Once you've registered, please come to our office at 4020 Call Field Rd Monday-Friday between the hours of 8a-10a or 1p-3p for a prescreen interview. Remember to wear your facial covering, please. We look forward to seeing you soon!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 searching for a Chemist to join a great manufacturing team here in Wichita Falls!Responsibilities:Quide Quality Control technician in testing of daily production batches and reviewing daily batch sheetsUpkeep and calibration of all lab instruments and suppliesTesting and qualification of raw materialsMaintain logs for all batches testedWork closely with all production supervisors to address any OOS batchesMethod development to test stability, performance, and quality of new and existing productsEstablish, modify, and create SOPs current and new test methodsUndertake special projects to formulate new products for customers. Maintain records to keep track of the development of new products and retention of all physical samplesRequires and extensive Chemistry background to understand the composition of active materials that will be used in the formulation of special productsWorking hours: 5:00 AM - 3:30 PMSkills:Extensive background in Chemistry, pay will depend on experience and educationExtreme attention to detailOrganization skills are a mustKnowledge of general safety practicesEducation:BachelorsExperience:1-4 yearsQualifications:High school diploma or equivalent requiredMust submit to background check and drug screen Please register at www.spherion.com/apply. Once you've registered, please come to our office at 4020 Call Field Rd Monday-Friday between the hours of 8a-10a or 1p-3p for a prescreen interview. Remember to wear your facial covering, please. We look forward to seeing you soon!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.

    Thank you for subscribing to your personalized job alerts.

    It looks like you want to switch your language. This will reset your filters on your current job search.