Pharmaceutical Quality Control Manager

Placements24; East London; Hybrid; ZAR 900,000 - 1,500,000; Full time

Benefits offered by this job

Medical aid

Life insurance

Retirement fund

Performance bonuses

Job summary

Placements24 seeks an experienced Pharmaceutical Quality Control Manager to lead the QC department in East London, Eastern Cape. You will oversee a team of QC analysts, ensure GMP compliance, and drive analytical testing strategies to uphold product quality and patient safety.

The role requires a Bachelor's or Master's in a life science, 7+ years in pharmaceutical QC with 3+ in management, and strong regulatory knowledge including SAHPRA.

Qualifications

• Bachelor's or Master's in Pharmacy, Chemistry or related life science.
• 7+ years in pharmaceutical QC with 3+ years in a supervisory role.
• Strong GMP knowledge and regulatory understanding (SAHPRA).
• Experience in method development, validation and transfer.

Responsibilities

• Lead, manage and mentor the QC laboratory team and ensure efficient operation.
• Oversee testing of raw materials, in-process samples and finished products.
• Develop, validate and transfer analytical methods for new products.
• Ensure GMP compliance and adherence to regulatory guidelines (SAHPRA).
• Manage laboratory equipment calibration, maintenance and qualification.
• Review QA testing records, COAs and deviation reports.
• Investigate OOS results and implement CAPAs.
• Liaise with Production, QA and R&D to resolve quality issues.
• Manage budgets, inventory and vendor relationships.
• Stay updated on analytical advancements and regulatory changes.

Skills

Leadership

GMP knowledge

Regulatory compliance

Problem solving

Education

Bachelor's or Master's degree in Pharmacy/ Chemistry

Tools

HPLC

GC

UV-Vis

Karl Fischer

LIMS

MS Office

Job description

About the Role

Our client, a reputable pharmaceutical manufacturer, is seeking an experienced Pharmaceutical Quality Control Manager to lead their QC department in East London, Eastern Cape . This leadership role is crucial for ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. You will oversee a team of QC analysts, manage laboratory operations, and implement robust quality control procedures. The ideal candidate will possess extensive experience in pharmaceutical quality control, a deep understanding of GMP, and strong leadership and analytical skills. This position offers a significant opportunity to contribute to product quality and patient safety within a well-established company.

Key Responsibilities

• Lead, manage, and mentor the Quality Control (QC) laboratory team, ensuring efficient operation and professional development.
• Oversee the testing of raw materials, in-process samples, and finished products according to established specifications and validated methods.
• Develop, validate, and transfer analytical methods for new products and optimize existing methods.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines (e.g., SAHPRA).
• Manage laboratory equipment, ensuring proper calibration, maintenance, and qualification.
• Review and approve QC testing records, certificates of analysis, and deviation reports.
• Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
• Liaise with other departments, including Production, Quality Assurance, and R&D, to resolve quality-related issues.
• Manage laboratory budgets, inventory, and vendor relationships.
• Stay updated on the latest advancements in analytical techniques and regulatory requirements within the pharmaceutical industry.

Requirements

• Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related life science discipline.
• A minimum of 7 years of experience in pharmaceutical Quality Control, with at least 3 years in a supervisory or management role.
• Extensive knowledge of GMP, pharmaceutical analysis, and quality control systems.
• Proficiency in various analytical techniques such as HPLC, GC, UV-Vis, Karl Fischer titration, etc.
• Experience in method development, validation, and transfer.
• Strong understanding of regulatory requirements specific to pharmaceutical manufacturing.
• Excellent leadership, team management, problem-solving, and decision-making skills.
• Proficiency in laboratory information management systems (LIMS) and standard office software.
• Strong communication and interpersonal skills, with the ability to interact effectively with all levels of the organization.

Benefits

Our client offers a competitive salary, performance-based bonuses, and a comprehensive benefits package including medical aid, life insurance, and a retirement fund. We provide opportunities for professional growth through ongoing training, workshops, and support for professional development courses. The work environment in East London is collaborative and supportive, encouraging innovation and teamwork. We value work-life balance and offer a range of employee wellness programs. This role presents an excellent opportunity to lead a key department within a respected pharmaceutical manufacturer committed to delivering high-quality products.