Production Pharmacist: GPM

 

Recruiter:

Dalitso

Job Ref:

3341103276

Date posted:

Saturday, June 11, 2022

Location:

Midrand, South Africa


JOB SUMMARY:
-

JOB 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
  • Registered with South African Pharmacy Council
  • Preferably 2-3 years’ experience in Pharmaceutical Production in a Manufacturing environment
  • cGMP skills
  • Computer Literacy – MS Office (proficient in Excel, Word and PowerPoint)

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

 


 

 

 

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