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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Quality Product Lead

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timePlainville, MA, USA$104.1k - $156.2k

About the Job

Requirements

  • An advanced degree and 4 years of experience in quality assurance in a GMP-regulated pharmaceutical or biotechnology environment, or a bachelor's degree and 6 years of such experience, are required.
  • Preferred fields of study include Chemistry, Biology, Microbiology, Engineering, or a similar scientific, engineering, or related technical field.
  • Professional certifications such as ASQ CQE or CQA are valued.
  • Experience with risk-assessment methodologies and root-cause analysis is required.
  • Strong knowledge of FDA, EMA, and global GMP regulations, including 21 CFR Parts 210/211 and ICH guidelines, is required.
  • Expertise in quality systems, including investigations, CAPAs, change control, and document control, is required.
  • Proficiency with quality management systems and standard office software is required.
  • Strong technical writing and documentation skills are required.
  • Verbal and written communication abilities are required.
  • Project-management and organizational capabilities are required.
  • Analytical and problem-solving skills are required.
  • Ability to work independently and collaborate effectively in cross-functional teams is required.
  • Ability to work effectively with diverse teams is required.
  • A customer-focused mindset and attention to detail are required.
  • Fluency in English is required.

Responsibilities

  • Conduct risk assessments and lead investigations, manage CAPAs, and ensure adherence to global regulatory requirements.
  • Serve as a client-facing Quality Assurance representative and partner directly with customers from batch startup through disposition.
  • Provide timely customer communications about quality events, deviations, investigations, product-impact assessments, and other quality matters that may affect manufacturing operations, product release, or disposition timelines.
  • Engage proactively and communicate transparently to build customer relationships while ensuring quality and compliance expectations are met.
  • Provide technical leadership and oversight in GMP manufacturing environments and drive quality excellence and continuous improvement.

Desired Qualifications

  • Experience hosting regulatory inspections and customer audits is preferred.
  • Data-integrity and computer-system-validation experience is preferred.
  • Additional languages are valued.

About the Company

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Thermo Fisher Scientific makes and sells the instruments, chemicals, consumables and lab services that drug companies, hospitals, universities and industrial labs use for research, testing and production. Its products cover work from gene sequencing and protein analysis to diagnostic tests and lab freezers, and its distribution arm ships supplies to labs worldwide. Drug developers also hire it to run clinical trials and to manufacture medicines under contract. It earns money from consumables that labs buy again and again, along with instrument sales, service contracts and outsourcing fees. The company traces its roots to Thermo Electron, founded in 1956, which merged with Fisher Scientific in 2006, and it is based in Waltham, Massachusetts.

Company size
10,001+
Company stage
IPO
Headquarters
Waltham, MA
Founded
1956

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