Senior Quality Assurance Specialist
Company: Joul--
Location: Durham
Posted on: April 24, 2025
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Job Description:
Job Title: Senior Quality Assurance Specialist
For a complete understanding of this opportunity, and what will be
required to be a successful applicant, read on.
Location: Durham, NC
Hours/Schedule: Mon- Fri 8am- 5pm
Type: Contract
Overview
Leading pharmaceutical company looking for an experienced Senior
Quality Assurance Specialist. Ideal candidates should have at least
5 years of experience in the pharmaceutical industry.
Responsibilities
Preferred experience in the assessment and preparation of
manufacturing sites for Pre-Approval inspections by Regulatory
agencies for new products. Reporting to the Quality Assurance
Organization, will independently manage project assignments.
Must have strong demonstrated interpersonal, communication,
negotiation, and persuasion skills. Must have very strong
relationship building skills.
Immediate project support on review and approval of commissioning
and qualification (C&Q) documents to support project
delivery.
Provide QA support including critical / constructive review and
approval of GMP documentation such as Quality Agreements, Quality
Risk Assessments, URS, FAT, IQ, OQ, PQ, other technical documents,
change management, and manufacturing/batch documents to meet
schedule milestones.
Ensure all aspects of the project proceed in compliance with cGMP,
regulations, and our Company's Quality Management System.
Focusing on areas such as Qualification and Compliance covering
Manufacturing Equipment (isolator, restricted access barrier,
incubator, washer, autoclave, formulation vessel, lyophilizer,
etc.).
Review and approval of master batch records, executed records,
technical protocols, investigations, change controls, SOPs,
validation protocols, technical reports.
Consults on an as-needed basis with next level manager on more
complex decisions.
Requirements Quality Assurance professional with at a minimum a BS
Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering
(or equivalent) and at least 5 years experience in the
Pharmaceutical Industry.
Must have working knowledge of regulatory expectations for the
manufacture and testing of sterile pharmaceutical products with
experience in quality assurance oversight of sterile manufacturing,
sterile process validation and/or sterile process technology
transfer.
Must have 3 years of experience with development, review, and
approval of User Requirement (URS), FAT, Installation Qualification
(IQ), Operational Qualification (OQ), Performance Qualification
(PQ) for pharmaceutical and biotechnology manufacturing equipment,
facilities and utilities.
Benefits
System One offers eligible employees health and welfare benefits
coverage options, including medical, dental, vision, spending
accounts, life insurance, voluntary plans, and participation in a
401(k) plan.
Ref: #558-Scientific
Keywords: Joul--, High Point , Senior Quality Assurance Specialist, Other , Durham, North Carolina
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