Associate Scientist Data Review Biochemistry

Eurofins USA BioPharma Services; Lancaster (Lancaster County); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading biopharmaceutical company is seeking an Associate Scientist to support Data Review in their Biochemistry team. This entry-level role involves reviewing scientific reports under CGMP guidelines, ensuring data accuracy, and assisting with audits. Ideal for candidates looking to grow in a laboratory environment, this full-time position offers comprehensive benefits and a balanced schedule.

Benefits

Medical, dental, and vision insurance

401(k) with match

Paid holidays

Qualifications

• Related Bachelor's Degree in a LIFE SCIENCE (e.g., Chemistry, Biochemistry, Biology preferred).
• Experience in a laboratory or GMP pharmaceutical setting preferred.
• Authorization to work in the United States indefinitely without sponsorship.

Responsibilities

• Review laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
• Assist with internal audits and ensure regulatory compliance.
• Learn new techniques and comply with company policies.

Skills

Organizational skills

Communication

Attention to detail

Computer skills

Education

Bachelor's Degree in a Life Science

Job description

Job Description

Eurofins Biopharmaceutical is looking for an Associate Scientist to support Data Review of our Biochemistry team. The Associate Scientist position is an entry-level opportunity that will allow for hands-on development and growth in day-to-day activities supporting a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). The Data Review responsibilities include reviewing scientific reports under CGMP guidelines, assisting with internal audits, ensuring regulatory compliance, data tracking, and reporting.

This position offers a balanced schedule supporting both laboratory and data tracking operations, ideal for candidates interested in learning both aspects within a lab setting.

Employee Responsibilities and Qualifications:

• Ensure quality data delivery by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
• Review routine and non-routine data across multiple areas according to departmental, corporate, and client SOPs; understand analytical procedures; ensure compliance with GLP/GMP requirements.
• Experience in a laboratory or GMP pharmaceutical setting preferred.
• Demonstrate good organizational skills, ability to follow directions, and effective communication skills.
• Possess strong computer, scientific, and organizational skills.
• Exhibit excellent communication (oral and written), attention to detail, and ability to work independently or as part of a team.
• Learn new techniques, perform multiple tasks, keep accurate records, follow instructions, and comply with company policies.

Qualifications:

Minimum Qualifications:

• Related Bachelor's Degree in a LIFE SCIENCE (e.g., Chemistry, Biochemistry, Biology preferred).
• Authorization to work in the United States indefinitely without sponsorship.
• Degrees in Computer Science do not meet minimum qualifications.

Additional Information:

• This is a full-time position, Monday-Friday, 8 am - 4 pm, with overtime as needed.
• Applicants should reside within a commutable distance of Lancaster, Pennsylvania; no relocation assistance provided. This position is not remote.
• Eurofins Lancaster Labs offers comprehensive benefits, including medical, dental, vision, life and disability insurance, 401(k) with match, paid holidays, and more.

Eurofins is an equal opportunity employer committed to diversity and inclusion, including Disabled and Veteran applicants.

For more information, visit our website www.eurofinsus.com.