Analytical Sciences Quality Lead

January 15, 2026
$63 / hour
Apply Now

Apply for this job

Upload CV (doc, docx, pdf)

Job Description

Job Summary:

  • Provide Quality partnership and oversight to the Product Development Clinical Supply (PDCS) at the New Haven site and at external CLO/CMO’s.
  • The Analytical Sciences Quality Lead will provide quality oversight of internal /external testing, stability, analytical technical transfer and quality systems elements in a matrix environment.

Duties and Responsibilities:

  • Review of technical documents, analytical method validation and transfers for Phase I to III clinical products (including but not limited to biologics, synthetics, cell & gene therapy as well as combination products).
  • Quality oversight of assay validation and transfer programs internally and externally.
  • Review and approval of stability reports, analytical development, equipment qualification reports and verification reports.
  • Perform data verification on CMC sections for filings based on technical reports.
  • Partner with ADQC and PDCS Compliance team to manage the timely completion of QMS records (Change Controls, Deviations, LIRs and CAPA’s) aligned to Global quality metrics goals.
  • Proactively manage clinical product quality risks ensuring they are appropriately mitigated, actioned and escalated to senior management as required.
  • Supports analytical lifecycle management initiatives.
  • Partner with other Quality colleagues on product quality impact assessments, particularly for notifications to management, recalls, etc.

Education & Experience:

  • B.Sc./MS degree in biological /chemical sciences, or a related pharmaceutical sciences field or equivalent experience in regulated industry.
  • Preferable 8 years or more cGMP experience within quality assurance in a biotech, pharmaceutical, or biopharmaceutical manufacturing environment, clinical phases through commercial.
  • Prior experience with method validation and method transfers.
  • Strong analytical candidate with quality assurance experience and a background in clinical testing.

Knowledge, Skills and Abilities:

  • Strong analytical background.
  • Demonstrated ability in decision making, problem solving and project management.
  • Collaborate, negotiate, influence and lead in a matrix organization.
  • Excellent communication and interpersonal skills.
  • Knowledge of quality systems with a strong technical acumen required.

Interview:

  • 1 round of interview with the HM and Technical team.