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QC Physical Chemistry Scientist

Post Date:Jan 12, 2019Type:Full-Time
Start Date:1/12/2019Salary:
Location:US-CA-Fremont Job Reference:15299

Job Description:
QC Physical Chemistry Scientist

Employee Responsibilities:
  • Perform analytical (UV/Vis, qPCR, SDS-PAGE, Western blot, CGE), compendial testing (pH, osmolality, turbidity, turbidity, appearance), particulate analysis (HIAC, MFI, visible inspection), and drug product device functional testing (break loose/extrusion, auto injector functionality, container closure integrity) in a GMP environment
  • Conduct laboratory investigations, problem-solving and trouble-shooting for aberrant results
  • Review QC test results
  • Generate, review, and maintain detailed records/documents, and assist with QC data management and control charting
  • Prepare sample reconciliation reports, revise SOPs and training manuals, manage deviation and change control records
  • Participate in method validation and method transfer activities
  • Interface with other functional groups within and outside of QC
The Ideal Candidate would possess:
  • Aseptic processing, clean room operations, compliance, sample handling/receipt/distribution, BioMES, data management/archiving experience
  • Experience with LIMs, SAP, Trackwise, IDEA, and/or NWA
  • Experience in performing investigations related to biopharmaceutical quality issues
  • Demonstrated success in a GMP regulated analytical environment
  • Familiarity with Zwich, qPCR, icIEF
  • Critical thinking skills, ability to manage time, and attention to detail
  • Good knowledge of computer system validation, GMP and FDA, SUP and European regulations relating to material/product samples and testing
  • Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience
  • Demonstrated ability to work as an independent, self-motivated, detail-oriented, results-driven and highly flexible team player in a fast-paced working environment
  • Proficient computer skills and knowledge of Microsoft applications
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Minimum Qualifications:
  • Bachelor's degree in chemistry, biology, biochemistry, biotechnology, chemical engineering, or biochemical engineering discipline
  • 1 to 2 years of experience working in Quality Control within the Pharmaceutical or Biotech industry, in a GMP or GLP regulated laboratory environment
  • Authorization to work in the United States indefinitely without restriction or sponsorship
What we offer:
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
Position is full-time with overtime as needed. Candidates currently living within a commutable distance of Fremont, California are encouraged to apply.

Eurofins Lancaster Laboratories Professional Scientific Services ® (PSS) is a global, award-winning insourcing solution that places our people at our clients' site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.

We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client's quality systems and equipment.

To learn more about Eurofins Lancaster Laboratories, please explore our website .

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Contact Information
Name: Eurofins

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