Join Jamjoom Pharma as a Junior IPC Manager – Quality Department
Are you detail-oriented, driven, and passionate about quality assurance in the pharmaceutical industry? Jamjoom Pharma is seeking a dedicated Junior IPC Manager to join our Quality team and contribute to our mission of delivering excellence in healthcare.
Key Responsibilities:
- Team Leadership & Management: Lead, train, and develop the IPC team of Officers and Analysts. Schedule activities, manage workloads, and foster a culture of quality and accountability.
- System Management: Oversee the entire IPC system, including sampling plans, testing procedures, documentation, and trend analysis for all manufacturing stages (from dispensing to packaging).
- Quality Assurance: Ensure all in-process tests are performed accurately, on time, and documented as per SOPs.
- Deviation & OOS Management: Immediately investigate and report any failures, Out-of-Specification (OOS) results, or process deviations. Initiate and support root cause analysis and corrective/preventive actions (CAPA).
- Compliance: Guarantee that all IPC activities strictly adhere to cGMP, GLSP, data integrity principles (ALCOA+), and company SOPs. Serve as a point of contact during internal and external regulatory audits.
- Continuous Improvement: Analyze data to identify trends, potential risks, and opportunities for process optimization. Drive initiatives to improve efficiency, reliability, and quality of IPC operations.
- SOP & Documentation: Review, update, and authorize IPC-related Standard Operating Procedures (SOPs), batch records, and forms. Ensure all documentation is complete, accurate, and maintained.
- Cross-Functional Collaboration: Work closely with Production, Quality Control (QC), Quality Assurance (QA), and Engineering departments to resolve issues and ensure seamless production flow.
- Equipment & Lab Management: Ensure IPC instruments and equipment are calibrated, maintained, and suitable for use.
Qualifications & Experience:
- Bachelor’s degree in pharmacy
- Minimum of +10 years of hands-on experience in a pharmaceutical manufacturing environment, with at least 3 years in a supervisory or managerial role within IPC, Quality Control, or Production.
- Proven expertise in solid dosage forms (tablets, capsules) and/or liquid, semi-solid, sterile products is highly desirable.
- Technical Skills:
- In-depth knowledge of cGMP, WHO-GMP, ICH guidelines, and pharmaceutical manufacturing processes.
- Strong understanding of statistical process control (SPC) and quality management systems (QMS).
- Proficiency in using pharmaceutical manufacturing and laboratory equipment.
- Excellent documentation skills and familiarity with electronic document management systems (EDMS).
- Soft Skills:
- Strong leadership, problem-solving, and decision-making abilities.
- Excellent communication and interpersonal skills.
- High level of integrity, attention to detail, and a results-oriented mindset.
- Ability to work under pressure and manage multiple priorities.
