Senior Quality Control Analyst - Pharmaceutical Manufacturing

Placements24; Pietermaritzburg; Hybrid; ZAR 480,000 - 720,000; Full time

Benefits offered by this job

Competitive salary package

Medical aid and retirement fund

Professional development and training

Supportive team environment

Pietermaritzburg location

Job summary

Placements24 is recruiting a Senior Quality Control Analyst in Pietermaritzburg to uphold GMP/GLP standards in pharmaceutical manufacturing. You will lead analytical testing of materials and products, develop validated methods, and guide junior staff in a fast-paced lab environment.

The ideal candidate has 5+ years' QC/QA experience, strong data analysis skills, and excellent communication to collaborate with Production, R&D and Regulatory Affairs.

Qualifications

• Bachelor's or Master’s degree in Pharmacy, Chemistry, Biochemistry or related life science field.
• Minimum 5 years' experience in pharmaceutical Quality Control or Quality Assurance.

Responsibilities

• Conduct tests of raw materials, in-process samples and finished products using analytical techniques.
• Develop, validate and implement analytical methods as required.
• Troubleshoot and maintain analytical instrumentation; ensure calibration.
• Analyze and report complex data for management and regulatory bodies.
• Investigate OOS results and deviations; implement CAPA.
• Ensure GMP/GLP compliance and regulatory guidelines.

Skills

Quality control

Data analysis

Problem solving

Communication

Education

Bachelor's or Master's in Pharmacy, Chemistry, Biochemistry or related life science

Tools

HPLC

GC

UV-Vis spectroscopy

Titration

Job description

About the Role

Our client, a leading pharmaceutical entity, is seeking a highly motivated and experienced Senior Quality Control Analyst to join their dynamic team in Pietermaritzburg. This is a critical role responsible for ensuring the highest standards of quality and compliance in pharmaceutical product manufacturing. The successful candidate will play a pivotal role in upholding our client's commitment to producing safe and effective medications. This position offers a unique opportunity to contribute to a respected organization within the vibrant pharmaceutical landscape of KwaZulu-Natal. You will be instrumental in driving quality initiatives and ensuring all processes meet stringent regulatory requirements, fostering a culture of excellence and continuous improvement within the laboratory and manufacturing environment.

Key Responsibilities

• Conduct comprehensive testing of raw materials, in-process samples, and finished pharmaceutical products using a variety of analytical techniques.
• Develop, validate, and implement new analytical methods as required, ensuring accuracy and reliability.
• Troubleshoot and maintain analytical instrumentation, ensuring optimal performance and calibration.
• Analyze and interpret complex test data, preparing detailed reports for management and regulatory bodies.
• Investigate out-of-specification (OOS) results and deviations, recommending and implementing corrective and preventive actions (CAPA).
• Ensure all laboratory activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Mentor and provide technical guidance to junior laboratory staff.
• Participate in internal and external audits, providing necessary documentation and explanations.
• Collaborate with other departments, including Production, R&D, and Regulatory Affairs, to resolve quality-related issues.

Requirements

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related life science field.
• Minimum of 5 years of experience in a pharmaceutical Quality Control or Quality Assurance role.
• In-depth knowledge of analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Proven experience with GMP/GLP and regulatory requirements (e.g., SAHPRA, FDA).
• Strong understanding of pharmaceutical manufacturing processes and quality systems.
• Excellent problem-solving, analytical, and critical thinking skills.
• Proficiency in data analysis and report writing.
• Ability to work independently and as part of a team, with strong attention to detail.
• Excellent communication and interpersonal skills.

Benefits

• Our client offers a competitive salary package commensurate with experience and qualifications.
• Employees benefit from comprehensive medical aid, a retirement fund, and opportunities for professional development and further training.
• The company fosters a supportive and collaborative work environment, encouraging career growth within the pharmaceutical sector.
• Situated in the scenic city of Pietermaritzburg, you will enjoy a fulfilling career combined with a pleasant living environment.
• This role provides the chance to make a significant impact on public health through dedication to quality.