Eurofins Lancaster Laboratories

Regional Quality Manager

Eurofins Lancaster Laboratories • $125K — $140K *
Santa Clara, CA 95051In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Bachelor's degree or 5 years of related experience.
  • Minimum 2 years of experience on a TIC Quality Team.
  • Experience with internal and external audits.
  • Proficient in MS Office (Word, Excel, PowerPoint, Outlook).
  • Strong knowledge of ISO17025, ISO17020, and ISO17065.

Responsibilities

  • Manage segments of the Eurofins E& E Quality System including NCR and Complaints.
  • Conduct annual Internal Audits at assigned Eurofins E& E offices starting in 2025.
  • Lead External Audits including those by Accreditation Bodies and Customers.
  • Foster teamwork by assisting staff with Quality related issues and training needs.
  • Develop relationships with the GM of each assigned office.
  • Participate in Quality meetings and manage equipment/database records.

Benefits

  • Comprehensive medical coverage including dental and vision options.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.
Full Job Description
Regional Quality Manager responsibilities include, but are not limited to, the following:
  • Manage the segments of the Eurofins E&E Quality System covering the NCR, Complaints, and Policing the Mark Systems.
    • Review documentation, provide input including participating in group meetings when requested by other Regional QMs, for work they are performing for their assigned segments of the Eurofins E&E Quality System.
  • Responsible for conducting the annual Internal Audit at each of his assigned Eurofins E&E offices beginning 2025. Assist each of his assigned offices with being prepared for external audits, through success learned during internal audits.
  • Responsible for the QMS portion of Internal Audits at Eurofins E&E offices.
  • Lead all External Audits at each of his assigned Eurofins E&E offices. This includes audits by Accreditation Bodies, as well as by Customers. Work with the QMS Manager to have the QMS portion of each audit performed, with each Department leader to have the technical portions of each audit performed.
  • Assist with Partner Lab Audits of other Eurofins E&E locations (Europe and Asia), as applicable
  • Foster positive morale and teamwork by assisting the staff at each of their assigned Eurofins E&E offices with all Quality related issues including providing or arranging for additional training of the staff, and with RC & CAP development as part of the NCR process. Meet and get to know all team members and understand their role in the Eurofins E&E organization by department at each of his assigned Eurofins E&E offices. Establish yourself as a "team member" in each of these offices and help to create a "we are all working together towards achieving quality" atmosphere.
    • Develop a close/friendly working relationship with the GM of each of his assigned Eurofins E&E offices.
  • Participate in Impartiality considerations.
  • Participate in the regular Quality "Hot Topics" meetings with the Quality Manager Team.
  • Participate in Partner Lab meetings and Quality Team meetings.
  • Manage and maintain the equipment and critical consumables databases.


Qualifications

Basic Minimum Education Qualifications:
  • Bachelor's Degree or 5 years of related experience

Basic Minimum Qualifications:
  • Minimum 2 years of experience working on a TIC Quality Team
  • Documented experience in the following:
    • Auditing - completion of internal and external audits
    • Root cause Analysis and Corrective Action Planning
  • Proficient in MS Office (Word, Excel, PowerPoint and Outlook)
  • Able to stand or sit for long periods of time
  • Able to lift up to 25 pounds
  • Strong knowledge of ISO17025, ISO17020, and ISO17065
  • Experience on a Quality Team in the TIC industry
  • A good understanding of day-to-day business operations
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

The Ideal Candidate Possesses the Following:
  • Demonstrate strong teamwork, project management and collaboration
  • Strong computer 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

Position is full-time, working Monday - Friday 8:00 am - 5:00 pm, with overtime as needed. Candidates currently living within a commutable distance of Santa Clara, CA are encouraged to apply.
  • Compensation: $125,000 - $140,000
  • 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

About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry
Pharmaceuticals & Biotech
* Ladders Estimates

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