Associate Data Review Scientist
Eurofins BioPharma Product Testing North America
Summary
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.
Job description
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.
Employee Responsibilities and Qualifications
- 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.
- 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.
Qualifications
Minimum Qualifications:
- Bachelors Degree in a LIFE SCIENCE field such as Chemistry, Biochemistry, and Biology required
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Position is full-time, working 8:00 AM-5:00 PM Monday-Friday, plus overtime as needed. Candidates currently living within commutable distance to Lancaster, PA are encouraged to apply.
Requirements
- Bachelors Degree in a LIFE SCIENCE field such as Chemistry, Biochemistry, and Biology required
- 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
Benefits
- Medical Coverage
- Dental Insurance
- Vision Insurance
- Life Insurance
- Disability Insurance
- 401(k) With Company Match
- Paid Vacation
- Paid Holidays
Company overview
Eurofins BioPharma Product Testing North America is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide, providing comprehensive laboratory services for pharmaceutical, biopharmaceutical, and medical device companies. As a leading Contract Research Organization (CRO), the company offers extensive testing capabilities for drug substances, final products, intermediates, and starting materials for both small and large molecule drug products. Operating under GMP authorization, ISO 17025 accreditation, and ISO 9000 certification, Eurofins performs analyses according to international pharmacopeial standards including Ph. Eur., BP, USP, and JP. With over 2 million square feet of global laboratory capacity spanning 20 countries and more than 45 locations worldwide, the company maintains seven key US sites in Lancaster, PA; Portage, MI; Columbia, MO; Cary, NC; Charlotte, NC; Jacksonville, FL; and San Diego, CA. Their comprehensive service portfolio includes method development and validation, release testing, stability testing, characterization testing, residuals and impurities testing, extractables and leachables testing, viral clearance studies, and cell and gene therapy testing. The company's harmonized quality procedures, centralized LIMS, and secure 24-hour data access via LabAccess.com provide clients with consistent, reliable testing services that support drug development from early stages through commercialization.