Associate Scientist Data Review: Biochemistry

Eurofins BioPharma Product Testing North America; Lancaster (Lancaster County); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking an Associate Scientist to join their Biochemistry team. This entry-level role offers hands-on development in a laboratory setting, where you will support data review and scientific report analysis under CGMP guidelines. Ideal for candidates who wish to balance laboratory work with data management, this position provides an excellent opportunity for growth and learning. The company offers a comprehensive benefits package and values self-motivation and adaptability in its employees. If you're ready to embark on a rewarding career in life sciences, this is the perfect opportunity for you.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401(k)

Paid Holidays

Qualifications

• Bachelor's Degree in a Life Science such as Chemistry or Biochemistry.
• Experience in a laboratory or GMP pharmaceutical setting preferred.

Responsibilities

• Review laboratory data for accuracy and compliance with GMP/GLP regulations.
• Maintain good organizational skills and communicate effectively.
• Work independently and as part of a team.

Skills

Data Review

GMP/GLP Compliance

Organizational Skills

Computer Skills

Communication Skills

Education

Bachelor's Degree in Life Science

Job description

Join to apply for the Associate Scientist Data Review: Biochemistry role at Eurofins BioPharma Product Testing North America

Eurofins Scientific is an international life sciences company providing a range of analytical testing services to make life and the environment safer, healthier, and more sustainable. The company works with major global clients to ensure product safety, authenticity, and accurate labelling.

Job Description

Eurofins Biopharmaceutical seeks an Associate Scientist to support Data Review within our Biochemistry team. This entry-level role offers hands-on development and growth opportunities in a laboratory setting, supporting data review, scientific report analysis under CGMP guidelines, internal audits, and data tracking.

The position balances laboratory work and data management, ideal for candidates interested in both areas.

Responsibilities include:

1. Review laboratory data for accuracy, clarity, and compliance with GMP/GLP regulations.
2. Review routine and non-routine data across multiple areas according to SOPs, ensuring adherence to analytical procedures and regulatory standards.
3. Maintain good organizational skills, follow directions, and communicate effectively.
4. Utilize strong computer, scientific, and organizational skills.
5. Work independently and as part of a team, demonstrating self-motivation and adaptability.
6. Learn new techniques, perform multiple tasks, keep accurate records, and follow company policies.

Qualifications

• Bachelor's Degree in a Life Science (Chemistry, Biochemistry, Biology preferred).
• Authorization to work in the U.S. without restrictions or sponsorship.
• Experience in a laboratory or GMP pharmaceutical setting preferred.

Additional Information

This is a full-time position, Monday-Friday, 8am-4pm, with overtime as needed. Candidates must be within commuting distance of Lancaster, PA; no relocation assistance provided. The role is on-site, not remote.

Eurofins offers comprehensive benefits including medical, dental, vision, 401(k), paid holidays, and more. The company is an equal opportunity employer.