GMP Chemist

Job Description

Job Responsibilities and Requirements:

The position will be providing analytical support to biotherapeutic process development teams, specifically focusing on large molecules (proteins, polysaccharides, nucleic acids, etc.).

Candidates should have familiarity with several of the below laboratory techniques; they should also possess expertise/knowledge with:

· Good Manufacutring Practices

· Quantitative polymerase chain reaction (qPCR)

· Enzyme linked Immunosorbent Assay (ELISA)

· Ultraviolet and visual light spectroscopy (UV-Vis)

· Analytical chromatographic separations using HPLCs or UPLCs

Qualifications

Authorization to work in the United States indefinitely without restriction or sponsorship

• Candidates within a commutable distance of Chesterfield, MO are encouraged to apply

• Electronic laboratory notebook systems and/or GMP documentation practice

• Experience with Plate-based assays, qPCR and HPLC is required.

• Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related fields.

• 1-3 years of relevant GMP industrial experience 

• Preferred experience: 

  · Empower or OpenLabs Software

Additional Information

• Position is full-time, Monday to Friday 8:00AM - 5:00PM. Candidates currently living within a commutable distance of Chesterfield, MO are encouraged to apply.

  What we offer:

  · Comprehensive medical coverage, with dental and vision options

  · Life and disability insurance

  · Paid holidays and vacation. 

  #LI-EB1

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