Associate Data Review Scientist: Biochemistry
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
- 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.
- Must have a related Bachelors Degree in a LIFE SCIENCE field such as Chemistry, Biochemistry, and Biology.
- PLEASE NOTE: THIS IS NOT A COMPUTER SCIENCE ROLE - a degree in the life sciences is required
- Authorization to work in the United States indefinitely without restriction or sponsorship
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
- 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 as appropriate
Benefits
- comprehensive medical coverage,
- life and disability insurance,
- 401(k) with company match,
- paid holidays and vacation,
- dental and vision options.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
