Quality Assurance Associate I

Eurofins BioPharma Product Testing North America; Columbia Township (MO); On-site; USD 55,000 - 76,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Life insurance

Disability insurance

401(k) with company match

Paid vacation

Job summary

Eurofins USA BioPharma Services is seeking a QA-focused professional to contribute to quality assurance and client reporting within a fast-paced lab environment. The role involves reviewing laboratory reports for accuracy, participating in CAPA and change controls, and ensuring procedures align with regulatory standards.

Collaboration with scientific staff and clients is essential for success. This full-time position offers comprehensive benefits and requires candidates to reside within

Qualifications

• Bachelor's degree required in a relevant scientific field.
• Authorization to work in the United States indefinitely without sponsorship.

Responsibilities

• Meets all quality and productivity metrics and demonstrates teamwork.
• Reviews and approves/rejects completed client laboratory reports for accuracy and completeness; addresses deficiencies.
• Assist with implementation and monitoring of quality systems and procedures (e.g., CAPA, change controls, trainings).
• Reviews protocols, procedures, data, and reports to ensure compliance with regulatory requirements and SOPs.
• Keeps supervisor informed of significant issues or developments.
• Learn new tasks and remember processes associated with this role.
• Communicate with Scientific staff to resolve comments.
• Complete tasks under speed or productivity quotas.
• Communicate effectively with client staff.
• Conduct all activities safely and efficiently.
• Performs other duties as assigned.

Education

Bachelor's degree in Chemistry / Biochemistry / Biology or related field

Job 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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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.

Job Description

• 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.
• Assist with 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.
• 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

Qualifications

• Bachelor's degree 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.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

Position is full-time position, Monday - Friday 8:00am - 4:30pm. Candidates currently living 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

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.