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      • 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
      • $32.00 - $33.00 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:Supervise manufacturing personnel through task assignment, delegation, and follow-up in production of plasmid DNA conforming to GMP guidelinesAssist in scaling-up processes to meet growing demands.Write Standard operating proceduresExecute validation protocolsPrepare solutions and materials required for the process.Follow batch records or SOPs to conduct cell banking, fermentation and purification processes for plasmid DNA manufacture at research or GLP scale.Conduct miniprep, concentration and gel analysis to in-process samples of research and cGMP productions.Install, commission and troubleshoot equipment as needed.Responsible for documentation and maintenance of equipment, such as: documenting new equipment and equipment changes, changing temperature charts, conducting and documenting PM for certain equipment, etc.Working hours: 6:00 AM - 3:00 PMSkills:Possess leadership skillsExcellent written and verbal communication skillsAbility to work in a clean room environment for extended periods of timeAbility to wear and work in PPEEducation:AssociateExperience: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 Bio-processing, preferred Apply 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 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:Supervise manufacturing personnel through task assignment, delegation, and follow-up in production of plasmid DNA conforming to GMP guidelinesAssist in scaling-up processes to meet growing demands.Write Standard operating proceduresExecute validation protocolsPrepare solutions and materials required for the process.Follow batch records or SOPs to conduct cell banking, fermentation and purification processes for plasmid DNA manufacture at research or GLP scale.Conduct miniprep, concentration and gel analysis to in-process samples of research and cGMP productions.Install, commission and troubleshoot equipment as needed.Responsible for documentation and maintenance of equipment, such as: documenting new equipment and equipment changes, changing temperature charts, conducting and documenting PM for certain equipment, etc.Working hours: 6:00 AM - 3:00 PMSkills:Possess leadership skillsExcellent written and verbal communication skillsAbility to work in a clean room environment for extended periods of timeAbility to wear and work in PPEEducation:AssociateExperience: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 Bio-processing, preferred Apply 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.
      • 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.
      • Windsor, Wisconsin
      • Temp to Perm
      • $18.50 - $20.50 per hour
      • Various Shifts Available
      We are partnering with Intelligen, a division of ABS Global, working with amazing new technology! This is a wonderful entry level lab position operating production equipment for processing cell sorting technology. Join a global leader in bovine genetics based in Windsor, WI.Responsibilities:Operate production equipment for processing cell sorting technology. ??? Prepare for the production process. ??? Participate in continuous operational improvement. ??? Work with coworkers and supervisor to effectively troubleshoot equipment and process issues. ??? Anticipate potential problems and take preventative action. ??? Understand how your own actions impact others and use this information in decision-making. ??? Review documentation and check all calculations (e.g. tickets, labels, equipment reading). ??? Troubleshoot equipment and process problems. ??? Comply with safety requirements, SOP and manufacturing documentation. Qualifications: ??? Post-High School education preferred ??? Biotech certificate preferred ??? Experience in a laboratory or equivalent production environment highly preferred ??? Understand the theory and concepts behind cell sorting technology and processes ??? Exhibit detail oriented documentation skillsWorking hours: Various Shifts AvailableSkills:Excellent manual dexterity - Strong attention to detail and respect for quality assurance - Basic math skillsEducation:High SchoolExperience:0-1 yearsQualifications:Lives and displays the Genus ABS Values and behaviors at all times in their day to day ways of working. ??? Maintain professional verbal and written communications with co-workers, internal and external customers, and vendors at all times. ??? Be flexible with respect to job responsibilities and consistently strive to be an effective team member.??? Strive to advance your skills and display a willingness to accept future development. ??? Actively participate in Company training opportunities to further develop skills applicable to the department. ??? Gain a thorough understanding of the Company???s business and the department???s role within the company. Lives and displays the Genus ABS Values and behaviors at all times in their day to day ways of working. ??? Maintain professional verbal and written communications with co-workers, internal and external customers, and vendors at all times. ??? Be flexible with respect to job responsibilities and consistently strive to be an effective team member.??? Strive to advance your skills and display a willingness to accept future development. ??? Actively participate in Company training opportunities to further develop skills applicable to the department. ??? Gain a thorough understanding of the Company???s business and the department???s role within the company.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.
      We are partnering with Intelligen, a division of ABS Global, working with amazing new technology! This is a wonderful entry level lab position operating production equipment for processing cell sorting technology. Join a global leader in bovine genetics based in Windsor, WI.Responsibilities:Operate production equipment for processing cell sorting technology. ??? Prepare for the production process. ??? Participate in continuous operational improvement. ??? Work with coworkers and supervisor to effectively troubleshoot equipment and process issues. ??? Anticipate potential problems and take preventative action. ??? Understand how your own actions impact others and use this information in decision-making. ??? Review documentation and check all calculations (e.g. tickets, labels, equipment reading). ??? Troubleshoot equipment and process problems. ??? Comply with safety requirements, SOP and manufacturing documentation. Qualifications: ??? Post-High School education preferred ??? Biotech certificate preferred ??? Experience in a laboratory or equivalent production environment highly preferred ??? Understand the theory and concepts behind cell sorting technology and processes ??? Exhibit detail oriented documentation skillsWorking hours: Various Shifts AvailableSkills:Excellent manual dexterity - Strong attention to detail and respect for quality assurance - Basic math skillsEducation:High SchoolExperience:0-1 yearsQualifications:Lives and displays the Genus ABS Values and behaviors at all times in their day to day ways of working. ??? Maintain professional verbal and written communications with co-workers, internal and external customers, and vendors at all times. ??? Be flexible with respect to job responsibilities and consistently strive to be an effective team member.??? Strive to advance your skills and display a willingness to accept future development. ??? Actively participate in Company training opportunities to further develop skills applicable to the department. ??? Gain a thorough understanding of the Company???s business and the department???s role within the company. Lives and displays the Genus ABS Values and behaviors at all times in their day to day ways of working. ??? Maintain professional verbal and written communications with co-workers, internal and external customers, and vendors at all times. ??? Be flexible with respect to job responsibilities and consistently strive to be an effective team member.??? Strive to advance your skills and display a willingness to accept future development. ??? Actively participate in Company training opportunities to further develop skills applicable to the department. ??? Gain a thorough understanding of the Company???s business and the department???s role within the company.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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