Great opportunity working with a global leader in the pharmaceutical manufacturing industry. This role will be perfect for a GMP QA professional with a strong desire to grow within a leading organization, serving clients across the world to offer world-class biologics manufacturing and development services.
Salary & Benefits:
$75k + bonus, benefits and relocation
Responsibilities:
*Reviewing and closing manufacturing batch records and associated supporting documentation relating to release of cell therapy products
*Participation in all daily batch release meetings
*Management of various complex issues that relate to GMP quality and compliance
*Training site staff as required
*Demonstrating thorough understanding of Quality Systems, GMP and GDP
*Support Quality Management System and departmental tasks as assigned
Key requirements:
*Bachelor's Degree or Associate's Degree with equivalent experience in a scientific or engineering background
*Strong experience in a GMP environment
*Biopharmaceutical manufacturing background is preferred
*Knowledge General knowledge of Good Manufacturing Practices (cGMP) required
To apply for this position and put yourself under immediate consideration, send your CV to john.spring@secpharma.com or call +44 (0) 207 255 6650
