Industry: Business Services•
Less than 5 years
Posted 282 days agoby Branden Lynch
Support therapeutic virus program and oversee manufacture of clinical materials in compliance with current Good Manufacturing Practice (cGMP).
*** Manage team of manufacturing associates for large scale production of virus drug substances and drug product.
*** Improve recovery, throughput, and scalability to optimize viral product manufacturing process.
*** Review, approve, and maintain process development materials, equipment, methods for cGMP compliance, and scalability.
*** Develop and maintain documentation: batch records, Standard Operating Procedures, work instructions, log books, Safety Data Sheets, equipment maintenance logs, product specifications, and material specifications.
*** Work collaboratively with cross functional teams to ensure on time execution of production schedule and delivery of study drug.
*** Identify problems and risks in areas affecting operations.
*** Train team members in accord with cGMP standards and institutional Standard Operating Procedures.
Highly innovative organization with cutting edge research capabilities offers an industry competitive compensation package, tuition reimbursement, bonuses, full medical benefits, 401(k) retirement plan, life and disability insurance, numerous professional development opportunities, generous paid vacation time, and more!
Please reference #37463501 when responding.Education Requirements: Bachelor DegreeMinimum Experience Requirements: 2-5 yearsJob City Location: PhiladelphiaJob State Location: PAJob Country Location: USA