GMP Laboratory Technician Evening Shift

Eurofins USA PSS Insourcing Solutions; St. Louis (MO); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401(k) with company match

Paid vacation

Job summary

Eurofins USA PSS Insourcing Solutions is seeking team members to support scale-up and manufacturing of mammalian and microbial processes for clinical and toxicology supplies. The role involves GMP operations, analytical testing, data entry, and cross-functional collaboration.

Qualifications include an associate's degree or higher in biotechnology or related fields, 0–2 years of laboratory/manufacturing experience, and strong communication and MS Office skills.

Qualifications

• Minimum of 0–2 years of experience in a laboratory or manufacturing environment.
• Excellent oral and written communication skills.
• Maintains a safe work environment.
• Strong computer skills in Microsoft Word and Excel.

Responsibilities

• Set up, execution and evaluation of GMP manufacturing unit operations (seed train, bioreactors/fermenters, centrifugation, filtration, chromatography, UF/DF, conjugation and lyophilization).
• CIP, SIP, aseptic sampling, parts washing, documentation, work order generation, and data entry/evaluation.
• Collaborate with laboratory and cross-functional teams to support testing timelines and operations.
• Perform routine analytical, compendial, and general laboratory testing in a GMP-regulated environment.
• Conduct testing using pH, appearance, UV-Vis spectroscopy and other analytical methods.
• Accurately document testing activities and results and review data for accuracy and compliance.

Skills

Communication skills

MS Word

MS Excel

Team collaboration

Safety awareness

Education

Associate's degree or BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry or equivalent

Job description

Job Description

Eurofins PSS is looking for new team members for our team to help support and join our diverse team to help assist on scale up and manufacturing of mammalian and microbial fermentation/purification processes for clinical and toxicology supplies.

• Duties and responsibilities will include:
  • Set up, execution and evaluation of GMP manufacturing unit operations such as seed train, bioreactors/fermenters, centrifugation, filtration, chromatography, UF/DF, conjugation and lyophilization.
  • CIP, SIP, aseptic sampling, parts washing, documentation, work order generation, and data entry/evaluation.
  • Will require communication and interaction with various groups and leaders in collaboration!
  • Perform routine analytical, compendial, and general laboratory testing in a GMP-regulated environment.
  • Conduct testing using techniques such as pH, appearance, UV-Vis spectroscopy, and other applicable analytical methods.
  • Follow approved SOPs, test methods, specifications, and laboratory procedures.
  • Operate, maintain, and perform routine checks of laboratory instruments and equipment as required.
  • Accurately document testing activities and results in accordance with GMP and data integrity requirements.
  • Review and evaluate analytical data for accuracy, completeness, and compliance with established requirements.
  • Support sample preparation, testing, documentation, and laboratory investigations, as applicable.
  • Maintain compliance with GMP, safety, quality, and applicable regulatory requirements.
  • Collaborate with laboratory and cross-functional teams to support testing timelines and laboratory operations.

Qualifications:
Qualifications

Minimum Qualification:

• Associate's degree or BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry or equivalent.
• Requires a minimum 0 to 2+ years of experience in a laboratory or manufacturing environment (bioprocess or chemical process industry).
• Authorization to work in the United States indefinitely without restriction or sponsorship
• Excellent oral and written communication skills.
• Maintains a safe work environment
• Demonstrated capability to work as a team member in a matrix development team
• Strong computer skills in Microsoft Office required, especially MS Word, MS Excel.

Preferred Skills:

• Prior experience in a Biological Pilot Plant or Commercial Manufacturing setting is desired.
• Knowledge of fermentation and or downstream processing techniques.

Physical Requirements:

• Must be able to lift 40 lbs and stand for 8-hour shift.

Additional Information

Positions are full-time, Monday-Friday, 3:30 PM to 12:00 AM. with overtime as needed. Candidates currently living within a commutable distance of Chesterfield, MO are encouraged to apply.

What we offer:

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Yearly goal-based bonus & eligibility for merit-based increases

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.