GMP Bioprocess Technician – Evening Shift & Benefits

Eurofins PSS Insourcing Solutions; St. Louis (MO); On-site; USD 28,000 - 39,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins PSS Insourcing Solutions is seeking team members to support scale-up and manufacturing of mammalian and microbial fermentation/purification for clinical and toxicology supplies, helping ensure high-quality, safe products.

Duties include setting up, executing and evaluating GMP unit operations (seed train, bioreactors, centrifugation, filtration, chromatography, UF/DF, conjugation, lyophilization), CIP/SIP, aseptic sampling and documentation; collaboration with multiple groups.

Qualifications

• Associate's degree or BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry or equivalent.
• 0–2+ 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 ability to work in a matrix development team.

Responsibilities

• Set up, execution and evaluation of GMP manufacturing unit operations (seed train, bioreactors/fermenters, centrifugation, filtration, chromatography, UF/DF, conjugation, lyophilization).
• CIP, SIP, aseptic sampling, parts washing, documentation, work order generation, and data entry/evaluation.
• Collaborate with various groups and leaders in cross-functional teams.

Skills

Communication skills

Teamwork

MS Office proficiency

Education

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

Tools

Microsoft Office (Word, Excel)

Job description

Eurofins PSS Insourcing Solutions is seeking team members to support scale-up and manufacturing of mammalian and microbial fermentation/purification for clinical and toxicology supplies, helping ensure high-quality, safe products.

Duties include setting up, executing and evaluating GMP unit operations (seed train, bioreactors, centrifugation, filtration, chromatography, UF/DF, conjugation, lyophilization), CIP/SIP, aseptic sampling and documentation; collaboration with multiple groups.