Programmer Analyst 6 - .NET Developer
Job Title: Analytical Sciences Quality Lead
Job Type: W-2 Contract
Duration: 12 months
Location: New Haven, CT 60% Onsite
Position Summary
Our client is seeking an Analytical Sciences Quality Lead who will provide Quality partnership and oversight of internal /external testing, stability, analytical technical transfer and quality systems elements in a matrix environment.
Principal 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.
Qualifications
· 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 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.
Education
· B.Sc./MS degree in biological /chemical sciences, or a related pharmaceutical sciences field or equivalent experience in regulated industry.
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