Quality assurance auditor jobs in the Biotechnology & Pharmaceuticals industry

. Adecco has partnered with a pharmaceutical manufacturing company in Rockland County in their search for a full-time Quality Assurance Auditor to maintain both their internal manufacturing QA as well as the quality of products and services of their external vendors - labs, API suppliers, packaging, etc. The Quality Auditor will schedule and perform audits, document and make observations of manufa...
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Responsible for floor level support in a quality role, for Pharmaceutical Manufacturing Operations. In addition, individual is responsible for verification of sample collection, real time batch record review, log book verification, and guidance for operations with batch documentation. Responsible for issuing batch related documents during off-shift operations. Must possess and be able to apply cGM...
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Quality Assurance Auditor Job Description Shift: Monday- Friday 8:00AM- 5:00 PM Pay rate: $17 an hour Requirements: · Four year degree in a science related field, required. · Minimum of 2 years of applicable cGMP experience in QA position as deemed appropriate by QA management. · Though understanding of cGMP regulations and various regulatory body expectations · General understanding of aseptic ma...
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Job Summary: Support Quality Policy and Meridian Operating Procedures and provide cost effective solutions for success. Be actively involved with Quality Improvements and have a constant awareness of Customer Requirements. Be oriented to metric-driven decision making; accurate and concise record keeping; an awareness and upholding of 21 CFR, Part 820 and ISO 13485; partner with our internal custom...
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Reporting to the North America, R&D QA Director, the incumbent provides support to new product registrations in Merial. Implements procedures to ensure the integrity of all Merial research output intended for regulatory submissions. Major responsibilities include, but are not limited to, the following: Provide QA support to new product registrations for R&D. Audit assigned validation and material ...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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JOB SUMMARY: The Sr. Principal Specialist, in interaction with Management, is responsible for the development, implementation and management of specific audit activities and programs. These programs are designed to support stated goals for identified development activities both within the CSO Platform and to outside providers including investigators and CROs. The Sr. Principal Specialist is also r...
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Johnson & Johnson companies are equal opportunity employers. Supplier Quality Lead Auditor-5130121212 Description Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies Inc. is currently recruiting for a Staff Quality Engineer located in Skillman, NJ. Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies, Inc. develops an...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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The Senior Lead Quality Auditor is responsible for aiding in the development of and subsequent implementation of quality processes associated with site internal and external audits (Suppliers), Approvals, Quality Council, Management Reviews, risk assessments, and routine company reporting. All quality processes will be in compliance to 21CFR 820, ISO requirements. Contract thru December 2013. Main...
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Johnson & Johnson companies are equal opportunity employers. COMPLIANCE AUDITOR II-6577130423 Description McNeil Consumer Healthcare Division of McNEIL-PPC, Inc. is currently recruiting for a cGMP Compliance Auditor II, located in Lancaster,PA. McNeil Consumer Healthcare Division of McNEIL-PPC, Inc. markets a broad range of Over-The-Counter (OTC) products, including TYLENOL® acetaminophen products...
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Quality Auditor Principal Schedule and conduct internal audits,support external agency inspections (e.g. FDA, EMA, TGA and others), and external vendor/supplier audits and inspections. Prepare audit reports and initiate the subsequent corrective action requests. Assist in the management of external audits. Responsible to track and trend key audit program metrics, and to report at management review...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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Position Summary:Primary responsibility for cGMP Compliance for a total of five manufacturing facilities in New Jersey & New York.The facilities include two high volume solid oral dose manufacturing facilities and other manufacturing facilities for other dosage forms.Working closely with key business partners in Manufacturing, Facilities, Operations, Regulatory Affairs, Quality Control and R&D; th...
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Job Summary: The Principal Specialist is responsible for the initiation, conduct, and follow-up of audits as assigned by CQA Management. Within the frame of the Principal Specialist's mission and responsibilities, the audits and activities require proven ability to independantly interact with all internal and external (e.g. Vendors / CRO) operational staff (e.g. Project Teams, Clinical Operations,...
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License/Certification/Education: Normally B.A./B.S. in Science w/1-2 years of experience. Job Description: Conducts audits for the regulatory/QA function within the Clinical Trials Department in order to help assure compliance with GLP/GCP in accordance with established FDA regulations and company policies and standard operating procedures. Reviews data and reports emanating from laboratory Clinic...
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Posting date: March 4, 2013 Position Summary: Responsible for implementing and maintaining the effectiveness of the quality system. Ensures systems are established, effective and maintained in compliance with regulatory, corporate and site requirements and policies related to supplier control and management. Identify, leads and implements initiatives for the continual improvement of the supplier c...
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Johnson & Johnson companies are equal opportunity employers. Quality Engineer III, External Manufacturing QA Compliance-8143130515 Description Johnson & Johnson Consumer Products Company, a member of Johnson & Johnson Family of Companies, is recruiting for a Quality Engineer III, External Manufacuturing QA Compliance (EMQA) for its location in Skillman, NJ. Johnson & Johnson Consumer Products Comp...
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Aesculap is the largest worldwide supplier of surgical instruments and implants for all disciplines including neurosurgery, microsurgery, ENT, plastic and reconstructive, thoracic, micro-vascular, cardiovascular, orthopedic, laparascopic, general surgeries and central processing. We were founded in Germany in 1867 and have been in operation in the U.S. since 1977. Our U.S. corporate office is loca...
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Excellent opportunities for Quality Assurance personnel to join a rapidly growing R&D oriented service laboratory located in central New Jersey. Quality Assurance Auditor Responsibilities include but are not limited to: inspecting/auditing analytical/bioanalytical studies performed according to Good Laboratory Practices (FDA, EPA, and OECD); reviewing study data and reports; auditing software/syst...
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Quality Auditor will conduct routine audits of data, information, procedures, equipment and systems (including protocol approval), and/or facilities to ensure the compliance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs) and other applicable worldwide regulations. Review and approve production and analytical documentation accompanying the release of API, Safety Asse...
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Johnson & Johnson companies are equal opportunity employers. Supplier Quality Staff Engineer-4357130320 Description Johnson & Johnson Family of Consumer Products Company Division of Johnson & Johnson Consumer Companies, Inc. develops and markets baby care, wound care and skin care products that address the needs of consumers and health care professionals and incorporate the latest innovations. The...
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The position reports to the Director, RA & QA. Ensure quality system and regulatory compliance. Plan and execute closed-loop internal audits. Support import and export compliance. Prepare for and help host external audits with regulatory agencies including US FDA and Health Canada. Position requires a Bachelors Degree in Engineering, Science, or a related field. RAC &/or ASQ &/or related professio...
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Diagnostica Stago, Inc. is the exclusive provider of Diagnostica Stago Hemostasis product lines in the United States. Diagnostica Stago, Inc. offers a complete system of coagulation instruments and optimized reagent kits for research as well as for routine analysis. Total quality approach plays an integral part in the corporate culture at Stago. We are committed to a better understanding of hemost...
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