Quality Specialist - Rahway

This Quality Specialist position involves batch documentation review to ensure compliance with current Good Manufacturing Practices (cGMPs) regulations and relevant regulatory filing submissions. Key responsibilities include evaluating and disposing of clinical supply materials, ...

We are currently hiring within our Quality Team for a Quality Specialist. This role is ideal for a recent graduate who is looking to build a career in the food manufacturing industry. · Print and ensure the accuracy of the printed information on finished good labels and Certifica ...

The Senior Specialist, Global Development Quality Operations is responsible for independent approval of documentation to support GMP clinical supply drug product manufacture testing release and maintenance. · This person will also independently approve documentation accompanying ...

The Senior Specialist Quality Assurance role involves independent approval of documentation for GMP clinical supply drug product manufacture, testing, release, and maintenance. This includes reviewing batch documentation, data, information procedures equipment systems facilities ...

The Rahway based Senior Specialist, Global Development Quality Operations, is responsible for independent approval of documentation to support GMP clinical supply drug product manufacture, · testing, release, and maintenance in support of our company's clinical supply programs.Ad ...

The External Manufacturing Quality Senior Specialist is responsible for ensuring that all products supplied to Client Animal Health from North America-based Contract Manufacturers are manufactured packaged analyzed and distributed in accordance with regulatory and company require ...

This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. · ...

This position will support QA oversight of CTLs for CTO Vector External Manufacturing operations. · This role is accountable for oversight of routine Quality responsibilities related to outsourced testing · Deviationss CAPAs Change Controls Certificate of Analysis/Certificate of ...

+This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. · +Requires bachelors degree in Science or related discipline. · Minimum 3-5 years of experience working in a regulated GxP environment. · ...

The Global Supplier Quality, External QC - Vector will process external deviation and change records from our Contract Test Laboratories (CTL). Other duties may include; Coordinate shipping and testing of samples for lot release, PPQ, · PSQ and will compile vendor documentation t ...

This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. external from our CTLs. · This role is accountable for oversight of routine Quality responsibilities related to outsourced testing, Deviati ...

The Quality Specialist will coordinate the review, investigation, and corrective actions associated with product complaints with the responsible manufacturing facilities in accordance with Corporate and Divisional policies and procedures. · ...

This position is essential for the coordination and direction of quality assurance programs. · ...

Job summary:The Quality Assurance eSystem Specialists primary responsibility is to help assure the quality, integrity, and compliance of site Information Technology (IT) systems, · and maintain alignment between business process owners, end users, and other cross functional areas ...

The R&D Quality Specialist is responsible for administration of integrated and comprehensive quality systems and controls that are appropriate, effective, efficient and continuously improving in order to ensure that R&D functions are operating in full compliance with sound scient ...

The Quality Specialist is responsible for the administration of integrated and comprehensive quality systems and controls that are appropriate, effective, efficient and continuously improving in order to ensure that R&D functions are operating in full compliance with sound scient ...

The Training Specialist will include developing implementing and evaluating training programs and policies which support integration project needs in alignment with Clients compliance standards. · Key responsibilities will include:Develop and support revision of training procedur ...

This position provides quality oversight for material suppliers and vendors used to manufacture, package and test client clinical and commercial products in accordance with client policies ,standards, procedures and international cGMPs. · ...

This Quality Assurance role involves performing QA shop floor activities, ensuring manufacturing compliance with applicable procedures and batch records. · ...

We are looking for a Quality Systems Specialist to join our Quality Management team. This individual can be based in New Providence, NJ or Jackson, MI. · ...