Quality Assurance Associate III
Eurofins BioPharma Product Testing Columbia, LLC

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.

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 Summary: Eurofins BPT Columbia is seeking a Quality Assurance Associate III to join their team in Columbia, MO on a full-time basis. This individual will provide assistance in improving quality processes and ensuring compliance with GMP and/or GLP systems and regulations.

Essential Job Duties:

• Applies GMP/GLP in all areas of responsibility, as appropriate
• Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
• Reviews and approves/rejects completed client laboratory reports and like records for accuracy, traceability, and completeness.
• Evaluates addressed deficiencies for clarification and for potential impact on compliance status.
• Works with staff to correct any noted deficiencies/inconsistencies.
• Implementation and monitoring of quality systems and procedures (e.g. CAPA, change controls, trainings, etc.)
• Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods, and SOPs.
• Keeps supervisor informed of significant issues or developments identified during quality assurance activities.
• Performs internal, external, and quality audits (cGMP, GLP, DEA, etc.)
• Develops content and format of training materials for cGMP and/or GLP and QA.
• Executes training for new and existing employees.
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Qualifications

Minimum qualifications:

• Bachelor's degree in chemistry, biochemistry, biology, pharmaceutical sciences, or other related degree concentration
• 5 years of directly related experience performing quality assurance in a cGMP/GLP environment
• Authorization to work in the U.S. without restriction or sponsorship

Additional Information

The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates within a commutable distance of Columbia, MO are encouraged to apply.

• 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

To learn more about Eurofins, please explore our websitewww.eurofinsus.com.

Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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