GMP Chemist

Eurofins

St. Louis (MO)

On-site

USD 65,000 - 90,000

Full time

2 days ago
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Benefits offered by this job

Comprehensive medical benefits
Life and disability insurance
Paid holidays and vacation

Job summary

Eurofins Scientific is seeking a biotherapeutic process development analyst to support large molecule analytical work. The role involves applying qPCR, ELISA, UV-Vis spectroscopy, and HPLC/UPLC techniques to drive method development and data generation in a GMP environment.

The candidate should have 1-3 years of GMP industrial experience and hold a Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, or Chemical Engineering, located within commuting

Qualifications

  • Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or related fields.
  • 1-3 years of relevant GMP industrial experience.
  • Experience with Plate-based assays, qPCR and HPLC is required.
  • Electronic laboratory notebook systems and GMP documentation practice.
  • Commutable distance to Chesterfield, MO.

Responsibilities

  • Provide analytical support to biotherapeutic process development teams focusing on large molecules.
  • Utilize qPCR, ELISA, UV-Vis spectroscopy, and chromatographic methods (HPLC/UPLC) to generate high-quality analytical data.

Skills

qPCR
ELISA
UV-Vis spectroscopy
GMP practices

Education

Biotechnology / Biochemical Engineering / Analytical Chemistry / Chemical Engineering (Bachelor's or Master's)

Tools

HPLC
UPLC

Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.


Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.


The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.


In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.


In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.


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

  • 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

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.

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

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