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SQA Services is seeking a Program Coordinator - Level 1 to assist in daily administrative tasks, data entry, and program administration. Responsibilities include coordinating program events, distributing technical materials, and maintaining database accuracy. This role offers exposure to international business relations and the Quality industry with growth potential.
Perform quality audits at suppliers to SQA's clients in the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries. Coordinate, prepare, execute, and deliver supplier quality audits based on client audit schedules. Apply skills and experience within the parameters of each program to produce consistent results for integration into client's supplier risk management framework.
Join our client as a Supplier Quality Engineer to conduct assessments, manage quality systems, perform root cause analysis, collaborate with suppliers and internal teams, and drive continuous improvement in supplier processes.
Perform quality audits at suppliers to SQA's clients in the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries. Coordinate, prepare, execute, and deliver supplier quality audits based on client audit schedules. Apply skills and experience within the parameters of each program to produce consistent results for seamless integration into client's supplier risk management framework.
The Administrative Assistant role involves coordinating travel arrangements, organizing meetings, handling office supplies, supporting corporate events, managing expense reports, and providing general administrative support to the executive team. Requires strong organizational, communication, and time management skills.
Performing Quality System and GMP compliance audits for suppliers in the Pharmaceutical or Cosmetics manufacturing industries. Familiarity with pharmaceutical manufacturing processes and GMP regulations is required. Strong QMS/GMP auditing experience needed. Good English communication skills essential.
Senior Quality Auditor responsible for performing quality audits at suppliers in the life sciences industry. Must have at least five years of experience and expert knowledge in GMP regulations. Required to be familiar with specific commodities and tools in the manufacturing environment.
Senior Quality Auditor responsible for assuring quality in the supply chains of life sciences clients. Performs quality audits at suppliers, applies skills and experience to produce consistent results. Requires expertise in GMP regulations and specific commodities/tools.
Responsible for performing Quality System and GMP compliance audits of Suppliers in healthcare and life science manufacturing industries. Must have strong QMS/GMP auditing experience and be familiar with pharmaceutical and medical device manufacturing processes. Must meet minimum qualification of EU GDP Auditor. Deployed based on subject matter expertise relative to manufacturing environment.
Senior Quality Auditor responsible for assuring quality in the supply chains of clients in the life sciences industry. Performing quality audits at suppliers, aligning expert findings with client programs, and integrating audit results into supplier risk management frameworks.
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