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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labeling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

 In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins BioPharma Product Testing has delivered expert scientific support to companies working to improve human and animal health. As a member of the Eurofins BPT team, you will work alongside respected technical experts dedicated to scientific excellence in a process driven regulatory compliant environment.  

Higher level quality assurance position which provides assistance in
improving Eurofins BPT-Columbia's quality processes and ensuring
compliance with GMP and/or GLP systems and regulations.

Essential Duties and Responsibilities:

• Applies GMP/GLP in all areas of responsibility, as appropriate
• Applies the highest quality standard in all areas of responsibility
• Demonstrates and promotes the company vision
• Demonstrates strong client service skills, teamwork, and collaboration
• Proactively plans and multitasks to maximize productivity
• Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
• Regular attendance and punctuality
• 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. Organizes and presents training sessions to groups or individuals
• May perform the essential job duties and responsibilities of management/GL to cover for vacations and extended absences.
• Learn new tasks and remember the processes associated with this role.
• Ability to communicate with Scientific staff for resolving comments
• Ability to complete tasks in situations that have a speed or productivity quota.
• Communicates effectively with client staff members
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

To perform this job successfully, the individual must be able to
perform each essential duty satisfactorily. The requirements below
are representative of the knowledge, skill or ability required. Attention
to detail is a must for this position, you must be able to read and
comprehend SOPs/Methods/Protocols/Specification and apply that to
data/reports that will be reviewed.

Bachelor's degree plus 5 years of directly related experience is
required. A degree in a relevant field such as chemistry, biochemistry,
biology, chemical engineering, pharmaceutical science, or other
directly related field or degree with comparable coursework is
preferred. In some cases, comparable demonstrated competence and
experience in the relevant area may be used to substitute in whole or
in part for the Bachelor's degree.

Position is full-time, Monday-Friday, 8 a.m.-4:30 p.m., with overtime as needed.  Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.

As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.  We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and PTO, and dental and vision options.

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

We are looking forward to receiving your application including your expected salary and possible start date via our career website.

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