Associate Scientist Data Review: Biochemistry

Eurofins • Lancaster, PA

102d • Onsite

About The Position

Eurofins Biopharmaceutical is looking for an Associate Scientist to support Data Review of our Biochemistry team. The Associate Scientist position is considered 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 requirement of this position will also allow for development and assignment of responsibilities that include reviewing scientific reports under CGMP guidelines, assisting with internal audits, review of scientific reports to ensure regulatory requirements have been met, data tracking and reporting. This position will provide a balance schedule to support both laboratory and data tracking operations and is seeking a potential candidate that is interested in learning both aspects within a lab setting.

Requirements

• Must have a related Bachelor's Degree in a LIFE SCIENCE. Chemistry, Biochemistry, and Biology Degrees are preferred.
• Authorization to work in the United States indefinitely without restriction or sponsorship.
• Experience in a laboratory setting or GMP pharmaceutical setting.
• Good organizational skills; ability to follow direction and good communication skills are required.
• Strong computer, scientific, and organizational skills.
• Excellent communication (oral and written) and attention to detail.
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

Responsibilities

• Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
• Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs.
• Read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility.
• Assist with internal audits and ensure compliance with regulatory requirements.
• Track and report data accurately.

Benefits

• Comprehensive medical coverage
• Life and disability insurance
• 401(k) with company match
• Paid holidays and vacation
• Personal days
• Dental and vision options

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: Bachelor's degree