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Mwn1yf5zc34dq013712

QC Scientist/Group Leader

Eurofins Berkeley Full-Time
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QC Scientist/Group Leader

Employee Responsibilities:
  • Lead and manage team members
  • Identify and resolve service and personnel problems in a timely manner
  • Troubleshoot methods and instrumentation
  • Write protocols and technical reports
  • Ensure project deliverables are scientifically accurate and meet timeline expectations
  • Perform compendial, as well as wet chemistry testing 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
  • Revise SOPs and training manuals, manage deviation and change control records
  • Interface with other functional groups within and outside of QC
The Ideal Candidate would possess:
  • Experience in performing investigations related to biopharmaceutical quality issues
  • Demonstrated success in a GMP regulated analytical environment

  • Critical thinking skills, ability to manage time, and attention to detail
  • Good knowledge of GMP 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
  • 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
  • Leadership in a dynamic team environment
  • Ability to drive performance by tracking and managing key performance indicators using internal and external metrics
Minimum Qualifications:
  • Bachelor's or Master's degree in chemistry, biology, biochemistry, biotechnology, chemical engineering, or biochemical engineering discipline
  • 5 to 7+ years of experience working in a Quality Control laboratory setting
  • Strong knowledge of cGMP or cGLP regulations
  • 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 Berkeley, 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 www.eurofinsus.com .

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

 

Recommended skills

Product Quality Assurance
Chemistry
Verbal Communication
Attention To Detail
Biochemistry
Biotechnology
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Job ID: 18745

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Eurofins Lancaster Laboratories is one of the largest commercial contract laboratories in the world providing comprehensive laboratory services in the pharmaceutical, biopharmaceutical and environmental sciences in both our laboratories and our client facilities. Our goal is to be the premier provider of laboratory services worldwide while delivering an outstanding service experience.

We serve clients from a diverse range of businesses and industries including Fortune 100 Industrial companies, the world’s largest pharmaceutical/biopharmaceutical companies as well as virtual, small and mid-sized companies throughout the world. We also serve local and national governments.

With facilities in Lancaster, Pennsylvania; Portage, Michigan; and Dungarvan, Ireland we have a global capacity of 300,000 square feet. Our state-of-the-art facilities coupled with the highest level of instrument technology allow us to handle projects of virtually any scope and size.

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