In Process Co-Ordinator (Port Elizabeth) at Aspen Pharma Group

Responsibilities

In-Process Testing and Reporting

• Conduct in-process testing, compare samples, calculate, interpret, and record testing results.
• Record defect, out of specification results, reporting these as appropriate
• Complete required documentation, update and maintain databases and appropriate reports.
• Ensure that all documentation adheres to signing protocols.
• Handle, operate, maintain, and calibrate equipment according to SOPs.
• Comply to GMP/ GLP requirements at all times.

 Reporting and Record Keeping

• Gather and record information, statistics and evidence required for reporting.
• Compile standardised reports and consolidate documents.
• Retrieve supporting documentation and records to facilitate and support query resolution.

 Stakeholder Relations 

• Communicate with internal stakeholders to achieve work objectives, maintain relationships and to assist and convey information.

Requirements

Background/experience

• Grade 12
• 1 to 3 years’ pharmaceutical manufacturing experience
• Specific job skills
• Broad working knowledge of concepts, terminology and specialized reporting requirements