Entry Level Scientist - CGT
Eurofins BioPharma Product Testing North America
Summary
Perform a wide range of analyses (routine and non-routine) primarily but not limited to the molecular, cell biology, and virology test areas of Biopharmaceutical Services.
Job description
Job Description
Perform a wide range of analyses (routine and non-routine) primarily but not limited to the molecular, cell biology, and virology test areas of Biopharmaceutical Services.
- Review and evaluate raw data for acceptability
- Set up and validate new analytical or related processes used by the department
Skills/Experience
Cell culture, cell and molecular techniques, aseptic technique, PCR, ELISA, Plate Reader, Flow Cytometry, Flow Cytometer, Cell counting, HPLC, CE-SDS Page, Particle Size, DLS, pH, osmolality, and appearance testing.
Qualifications
Basic Minimum Qualifications:
- Bachelor's degree in biology, biochemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Preferred Qualifications
- 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
Additional Information
Working schedule will be Full-Time, First Shift, M-F 8am-4:30pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is NOT remote.
Requirements
- Bachelor's degree in biology, biochemistry, or other related degree concentration, or equivalent directly-related experience
- Authorization to work in the United States indefinitely without restriction or sponsorship
- Cell culture
- Cell and molecular techniques
- Aseptic technique
- PCR
- ELISA
- Plate Reader
- Flow Cytometry
- Flow Cytometer
- Cell counting
- HPLC
- CE-SDS Page
- Particle Size
- DLS
- pH
- Osmolality
- Appearance testing
- 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.