9 deviations opportunities in Philadelphia updated today
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About the Company Client’s Manufacturing Division (MMD) is dedicated to providing high-quality pharmaceutical and biotech solutions. Our mission is to innovate and excel in the manufacturing process while fostering a culture of collaboration and continuous improvement. About the Role The role involv
SanofiA leading pharmaceutical company located in New Jersey seeks a Senior Quality Assurance Compliance Specialist to ensure high-quality standards. Candidates should have a Bachelor's degree and 5-10 years of experience in Quality Compliance, including regulatory knowledge and the ability to communicate
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Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just loo
Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just loo
SUMMARY: This position is responsible for supporting operations by ensuring that the building and utilities are properly maintained to support GMP manufacturing and general facility operations. This support includes performing building and utility equipment inspections, diagnosing problems, scheduli
Job Title Bioprocess Technical Operations and Quality Assurance Intern Requisition JR000015695 Bioprocess Technical Operations and Quality Assurance Intern (Open) Location Horsham, PA Additional Locations Job Description Summary Job Description Keenova is a leading pharmaceutical company dedicated t
Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. F
AstraZenecaCell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. F
XERIMIS, INC*Position Summary** This position is responsible for managing investigations, deviations, client complaints, and CAPAs, in accordance with cGMP and Xerimis standards. *Position Reports to:** Packaging Operations Manager *Position Supervises:** None *Essential Duties and Responsibilities** The essent
Integrated Resources, Inc ( IRI )Qualifications: B.S./M.S. degree in appropriate engineering/scientific field Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry Previous experience in
Job Title: Deviation Management Specialist Location: West Point PA Duration: 12+ Months Qualifications: •B.S./M.S. degree in appropriate engineering/scientific field •Mini mum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Tech
Qualifications: • • B.S./M.S. degree in appropriate engineering/scientific field • Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry • Previous exper
Qualifications: B.S./M.S. degree in appropriate engineering/scientific field • Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry • Previous experienc
Spectraforce TechnologiesDeviation Management Specialist - I (Assistant) 12 months West Point, PA, USA, 19486 Description: Qualifications : *B.S./M.S. degree in appropriate engineering/scientific field *Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Enginee
Qualifications: Education Minimum Requirements: • B.S. degree in Engineering or Sciences. Required Experience and Skills: • Minimum one (1)+ year post-bachelor's degree experience in a GMP (good manufacturing practices) manufacturing and/or technical support of GMP manufacturing operations (or M.S.
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Description: Qualifications: • • B.S./M.S. degree in appropriate engineering/scientific field • Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry • P
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for Philadelphia. Actual salaries may vary depending on experience, company, and area.
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