Endo Pharmaceuticals Job – Malvern, PA
5500.00 $
Published date: 2025/07/21
Employment type: Full-time
- Location: Malvern, Pennsylvania, United States
Position: Quality Assurance Specialist
Location
Endo Pharmaceuticals, 1400 Atwater Dr, Malvern, PA 19355, United States
Company
Endo Pharmaceuticals
Salary
USD 5,500–7,000 gross per month
Working Hours
Full-time, Monday to Friday, 8:30 AM – 5:00 PM
Job Description
Endo Pharmaceuticals is seeking a motivated Quality Assurance Specialist to join our team in Malvern, PA. This role is central to ensuring regulatory compliance and product quality across our pharmaceutical operations. Candidates will be expected to bring strong attention to detail and an understanding of FDA and GMP guidelines to help maintain high-quality manufacturing standards.
Key Responsibilities
Conduct batch record reviews and product release activities
Support audits, regulatory inspections, and CAPA follow-up
Maintain quality systems including SOPs, deviations, and change controls
Work closely with production and laboratory teams to uphold quality
Analyze data and prepare quality reports
Requirements
Legal authorization to work in the United States
Bachelor’s degree in life sciences, chemistry, or a related field
Minimum 2 years of experience in pharmaceutical QA or similar role
Familiarity with FDA regulations, cGMP, and ICH guidelines
Strong written and verbal communication skills
Benefits
Competitive salary and annual bonus plan
Comprehensive health, dental, and vision insurance
401(k) with employer matching
Paid time off and holidays
Professional development and training programs
Modern campus with on-site cafeteria and fitness center
Endo Pharmaceuticals, 1400 Atwater Dr, Malvern, PA 19355, United States
Company
Endo Pharmaceuticals
Salary
USD 5,500–7,000 gross per month
Working Hours
Full-time, Monday to Friday, 8:30 AM – 5:00 PM
Job Description
Endo Pharmaceuticals is seeking a motivated Quality Assurance Specialist to join our team in Malvern, PA. This role is central to ensuring regulatory compliance and product quality across our pharmaceutical operations. Candidates will be expected to bring strong attention to detail and an understanding of FDA and GMP guidelines to help maintain high-quality manufacturing standards.
Key Responsibilities
Conduct batch record reviews and product release activities
Support audits, regulatory inspections, and CAPA follow-up
Maintain quality systems including SOPs, deviations, and change controls
Work closely with production and laboratory teams to uphold quality
Analyze data and prepare quality reports
Requirements
Legal authorization to work in the United States
Bachelor’s degree in life sciences, chemistry, or a related field
Minimum 2 years of experience in pharmaceutical QA or similar role
Familiarity with FDA regulations, cGMP, and ICH guidelines
Strong written and verbal communication skills
Benefits
Competitive salary and annual bonus plan
Comprehensive health, dental, and vision insurance
401(k) with employer matching
Paid time off and holidays
Professional development and training programs
Modern campus with on-site cafeteria and fitness center
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