| Job alert | Jobs 1 - 10 of 640 |
FDA Pharmacovigilance Auditor
SQA Services
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New York City, NY
... What you’ll need: You will need to have expertise in US FDA Pharmacovigilance regulations. You will need experience managing PV agreements with multiple parties and assertiveness dealing with difficult auditees. As an SQA Quality Auditor, you will ... - Apr 22
Lead Automation Engineer
Azzur of CA
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Rahway, NJ
... Ensure compliance with regulatory requirements (e.g., FDA, EMA, GMP) and industry standards (e.g., ISA-88, ISA-95) for automation systems and processes. Develop and implement procedures and protocols for system validation, change control, and ... - Apr 26
HCG - MES Engineer
Horizon Controls Group
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Manhattan, NY, 10001
... Compliance and Regulatory Support: Stay up to date with relevant regulatory guidelines and industry standards (e.g., FDA, GMP) pertaining to MES systems. Assist in ensuring compliance with these regulations through proper system configuration, data ... - May 02
Pharmacy Technician
Merck
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Rahway, NJ, 07065
... Responsibilities: Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administration (FDA). Ensure that product labeling is updated in accordance with FDA regulations ... - May 04
HR Ops Manager - Start Up
Oakleaf Partnership Limited
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Manhattan, NY, 10261
... Desired Skills and Experience Oakleaf Partnership is working with a fast growing, FDA approved pharmaceutical business to find their next HR Manager. This role will join a small yet ambitious HR function and will touch on all elements of HR. This ... - Apr 19
Quality Assurance Manager Clinical Lab
Planet Technology
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Secaucus, NJ, 07094
... This also requires strong knowledge of GCPs, ICH Guidelines and FDA regulations related to Clinical Research, and prior experience in Clinical Quality Assurance. Other requirements include a working overview of the drug development process, ... - Apr 21
Labeling Specialist
AA2IT
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Rahway, NJ
... • Quality check for label content and formatting as per FDA guidelines. • Support the team with the review, revising labeling. Will review labels on packaging, container, carton boxes. • Will prepare the label content following SOP’s and FDA ... - May 01
Regulatory Submissions Specialist (Pharma)
24 Seven Talent
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Manhattan, NY, 10261
... Regulatory Submissions Specialist Responsibilities: Assist in filling in knowledge gaps on FDA regulations for Advertising & Promotion Thoroughly understand the intricacies of each client’s Medical Legal Review (MLR) process, including working ... - Apr 25
Quality Assurance Manager
Astrix
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New York, NY
... Minimum of 8+ years of experience in pharmaceutical or healthcare industry related experience, 3+ years of quality assurance management experience Must have working knowledge of current Good Manufacturing Practices (cGMP), FDA regulations, and 21 ... - May 04
Labeling Specialist
Merck
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Rahway, NJ
... Responsibilities: • Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administration (FDA). • Ensure that product labeling is updated in accordance with FDA ... - May 01