What are the responsibilities and job description for the Senior Pharma QA Specialist-(IQ/OQ/PQ) position at T1 Energy Inc.?
Freyr is Hiring!!! For one our TOP Leading Global Pharmaceutical Client!!!
Job Title: Senior Pharma QA Specialist-(IQ/OQ/PQ)
Location: Durham, NC
Pay Rate: $55-$62/hr.
Benefits - That is 5 earned paid sick days, Matching 401k plan, Discounted health insurance from United Health Care.
Qualifications:
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.
Responsibilities:
Reporting to the Quality Assurance Organization, will independently manage project assignments. 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.
Regards,
Kriti S
Recruiter, Staffing Dept. (US Region)
1 (609)681-2343
kriti.shukla@freyrsolutions.com
Regional office Address : 150 College Road West, Suite 102, Princeton, NJ 08540
Website: www.freyrsolutions.com
Job Title: Senior Pharma QA Specialist-(IQ/OQ/PQ)
Location: Durham, NC
Pay Rate: $55-$62/hr.
Benefits - That is 5 earned paid sick days, Matching 401k plan, Discounted health insurance from United Health Care.
Qualifications:
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.
Responsibilities:
Reporting to the Quality Assurance Organization, will independently manage project assignments. 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.
Regards,
Kriti S
Recruiter, Staffing Dept. (US Region)
1 (609)681-2343
kriti.shukla@freyrsolutions.com
Regional office Address : 150 College Road West, Suite 102, Princeton, NJ 08540
Website: www.freyrsolutions.com
Salary : $55 - $62
