Aspen Pharma Group Vacancies 2023 | In Process Quality Officer Vacancies in Port Elizabeth Apply Online Now

Aspen Pharma Group

Aspen Pharma Group Is Currently Seeking for In Process Quality Officer Position suitable candidate who is eligible to handle all the responsibilities and is qualified for the position. All the information required for this position to know by the candidate is given below specifically. apply online for this position by clicking on the apply now button and fill the Aspen Pharma Group application Form. The Position Is available in Port Elizabeth, Eastern Cape the candidates nearby willing to apply are also invited to apply online for this vacancy.

Hiring Authority: Aspen Pharma Group Careers

Position: In Process Quality Officer Jobs

Location: Port Elizabeth, Eastern Cape

Qualification: Matric, Grade 12, Diploma/ Degree

Salary Estimated: ZAR 72000-340000 Annum

Job Requirements & Responsibilities


Monitor product quality throughout the manufacturing and packaging process. Monitor QMS compliance with GMP standards as well as assist with deviations and quality investigations. Provide input into SOPs to ensure compliance and complete any related administrative tasks.



Planning and Processes

  • Plan and coordinate administrative activities
  • Provide recommendations on process improvements

In-Process Quality Management

  • Verify production plans for operation effectiveness
  • Perform line opening visual inspections as per checklist
  • Perform end-of-batch internal inspections to assess compliance and effectiveness of overall QMS
  • Perform on-line inspections of batch documents during manufacturing and packaging process to assess compliance
  • Perform inspections to monitor GMP compliance during manufacturing ? Perform inspection of logbooks, SOP files and AQL
  • Perform final inspection of finished goods
  • Raise deviations for non-conformances identified
  • Record and report quality problems as they are identified
  • Compile and issue report on non-conformances and ensure adequate CAPA plans have been implemented
  • Assist with product and quality investigations
  • Review and provide input into SOPs to ensure compliance to GMP standards and product specifications
  • Establish and apply continuous improvement processes
  • Monitor and audit compliance to regulatory and in-house standards with regards to current GMP
  • Participate in audits when required
  • Participate in unit risk assessments


  • Coordinate and consolidate the gathering of information for reporting
  • Compile detailed reports and documents
  • Monitor and control data integrity in all databases


  • Communicate with employees and management, to assist and convey information

Skills Required


  • Grade 12 with 6+ years’ related experience, or 2 year Diploma with 4+ years’ related experience
  • Pharmaceutical manufacturing experience

Specific job skills

  • Strong working knowledge of pharmaceutical quality operations and quality management systems
  • Pharmaceutical standards and compliance requirements
  • Ability to interpret and implement policies, processes and objectives


  • Information Gathering
  • Following Procedures
  • Capturing Facts
  • Taking Action

Fill The Aspen Pharma Group Application Form From the Link Given Above And Wait For the application to be processed once your application gets shortlisted you will be informed by the authority and called for the interview or examination processed by the company. Good luck For your job Search!

To apply for this job please visit

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