Description:
- Providing best practice day-to-day manufacturing pharmaceutical services to manage workflow, production and document procedure compliance so as to ensure safe and efficacious medicines are manufactured.
Qualifications and Experience:
- Pharm Degree
Outputs:
Lead training on SOP, departmental inspection, and audits (both internal and external) Online and in line testing resulting in approval of batch documentation and Provisional releases Submission of full production manufacturing tickets and supporting documentation within 24 hours of batch completions Ability to identify, execute and prioritize work tasks/projects Excellent interpersonal, communication skills and collaborative Strong problem solving and troubleshooting capabilities Improve production efficiency and reduce overtime Proper documentation of manufactured pharmaceutical products Perform Line Openings and Closures in manufacturing lines Prepare weekly production scheduling of product Auditing batch documents for QA closure and release Assist in preparing Annual Product Quality Reviews Initiate, investigate and close off CAPAs and Non-Conformances. Ensure regulatory compliance Safety, Health and Environmental Standards. Oversight on manufacturing process including in-process checks Regulatory and document compliance Handling of non-conforming production, both inbound, WIP and produced batches Audits and continuous improvement capabilities Development of team’s technical capabilities Lead / champion change overs, line opening, line closing, Lead and be the chief accountable officer for GMP and micro compliance in the area on shift
10 Jun 2022;
from:
gumtree.co.za