Greenfield Global Inc.-posted 3 months ago
Full-time • Senior
Brookfield, CT
51-100 employees

Greenfield is looking for a Quality Control Supervisor to join our growing team. This is a senior-level position responsible for overseeing and supporting the work of junior chemists, managing, and maintaining lab instruments, analyzing data, identifying quality issues, and leading and managing validation projects. The primary responsibility of the QC Supervisor will be to lead and supervise the QC department, ensuring regulatory compliance and maintaining high-quality standards. You will be accountable for mentoring and managing a team of QC chemists and analysts.

  • Conduct routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples for product release.
  • Utilize various analytical testing techniques such as Gas Chromatography (GC), UV-Visible spectroscopy, titrations, and other relevant methods.
  • Provide guidance, support, and mentorship to foster professional growth and development within the team.
  • Monitor compliance with established procedures, protocols, and regulatory requirements.
  • Represent the QC department in cross-functional meetings and project teams.
  • Review and revise quality control protocols and test plans to align with industry standards.
  • Plan, schedule, and coordinate analytical testing activities.
  • Monitor the generation of analytical data by the QC team to ensure accuracy, integrity, and compliance.
  • Assist the QC team in resolving technical problems related to instrumentation, method development, or other analytical issues.
  • Interact with internal and external customers to ensure proper sampling, reporting, and resolution of questions and concerns.
  • Lead investigations into Out of Specification (OOS) test results, deviations, and non-conformances.
  • Review, approve and validate data provided by other QC chemists.
  • Maintain audit readiness within the department by collaborating with a cross-functional team.
  • Provide technical review and approval of analytical test methods, validation protocols, risk assessments and Standard Operating Procedures (SOPs).
  • Manage validation protocols, including drafting, execution, and comprehensive documentation.
  • Ensure all team members are trained in safety procedures, GMP requirements and laboratory best practices.
  • Bachelor’s or master’s degree in chemistry, biochemistry, or a related field.
  • Previous experience in a QC or quality role.
  • 3+ years of experience in supervisory or leading role.
  • Strong supervisory, leadership, strategic thinking, and problem-solving skills.
  • Excellent communication and organizational skills.
  • Ability to manage multiple priorities under tight deadlines.
  • Base salary dependent on experience and demonstrated performance.
  • Formal and informal training opportunities.
  • Comprehensive health and dental benefits.
  • Income protection: short- and long-term disability coverage, life insurance, paid personal sick time.
  • Vacation time exceeding industry standards.
  • Company funded retirement savings program with individual contribution opportunities.
  • Meaningful and challenging work.
  • Curated intentional culture focused on growth and development, engagement, and communication.
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