Quality Control Analyst - Pharmaceutical Manufacturing

Placements24; Stellenbosch; On-site; ZAR 360,000 - 540,000; Full time

Benefits offered by this job

Medical aid benefits

Provident fund

Professional development and training

Modern well-equipped laboratory

Safe and collaborative work enviro n m

Growth opportunities

Job summary

Placements24 in Paarl, Western Cape seeks a meticulous Quality Control Analyst to perform laboratory tests ensuring raw materials, in-process samples, and finished products meet safety and efficacy standards. You will work in a modern, well-equipped facility, operate HPLC, GC, UV-Vis spectrophotometry, and Karl Fischer titration, and document findings under GLP and GMP.

Ideal candidates have a National Diploma or BSc in Chemistry or related field and 2–3 years pharma QC experience, with strong

Qualifications

• National Diploma or Bachelor's degree in Chemistry, Biotechnology or related science.
• 2–3 years' experience as a Quality Control Analyst in pharma or regulated industry.
• Hands-on experience with HPLC, GC, UV-Vis, and Karl Fischer titration.
• Strong GMP/GLP understanding and data analysis skills.
• Detail-oriented with good organizational and communication skills.

Responsibilities

• Conduct routine laboratory testing on raw materials, intermediates and finished products using analytical techniques.
• Prepare samples, reagents and media for testing.
• Calibrate and maintain laboratory equipment for accuracy.
• Document results per GLP and GMP.
• Investigate OOS results and participate in root cause analysis.
• Prepare CoAs for released batches.
• Participate in internal audits and inspections.
• Contribute to continuous improvement in QC.

Skills

GMP/GLP knowledge

Lab data analysis

Attention to detail

Time management

Teamwork

Education

National Diploma or Bachelor's degree in Chemistry/ Biotechnology or related science

Tools

HPLC

GC

UV-Vis spectrophotometry

Karl Fischer titrator

Job description

About the Role

Our client, a leading pharmaceutical manufacturer, is looking for a meticulous and detail-oriented Quality Control Analyst to join their state-of-the-art facility in Paarl, Western Cape . In this critical role, you will perform a variety of laboratory tests and analyses to ensure the quality and consistency of raw materials, in-process samples, and finished pharmaceutical products. Your work will directly contribute to ensuring that our client's products meet the highest standards of safety and efficacy. This is an excellent opportunity for a motivated individual to advance their career in pharmaceutical quality control within a supportive and technologically advanced environment in Paarl, Western Cape . We are seeking a proactive team player who is dedicated to maintaining product integrity.

Key Responsibilities

• Conduct routine laboratory testing on raw materials, intermediates, and finished products using various analytical techniques (e.g., HPLC, GC, spectroscopy, titration).
• Prepare samples, reagents, and media required for testing.
• Calibrate and maintain laboratory equipment to ensure accurate and reliable results.
• Document all laboratory activities, test results, and observations in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Investigate out-of-specification (OOS) results and deviations, and participate in root cause analysis.
• Assist in method validation and transfer activities.
• Maintain a clean and organized laboratory environment, adhering to safety protocols.
• Prepare Certificates of Analysis (CoAs) for released batches.
• Participate in internal audits and inspections as required.
• Contribute to continuous improvement initiatives within the QC department.

Requirements

• National Diploma or Bachelor's degree in Chemistry, Biotechnology, or a related science field.
• Minimum of 2-3 years of experience as a Quality Control Analyst, preferably within the pharmaceutical or a related regulated industry.
• Hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry, and Karl Fischer titrators.
• Strong understanding of GMP and GLP principles.
• Proficiency in laboratory calculations and data analysis.
• Excellent attention to detail and accuracy in performing tests and documenting results.
• Good organizational and time management skills.
• Ability to work effectively both independently and as part of a team in a laboratory setting in Paarl, Western Cape .
• Familiarity with pharmaceutical manufacturing processes is a plus.
• Good written and verbal communication skills.

Benefits

• Our client offers a competitive salary commensurate with experience and qualifications.
• Employees receive comprehensive medical aid benefits, a provident fund, and opportunities for professional development and further training.
• You will work in a modern, well-equipped laboratory with opportunities to learn new techniques and technologies.
• Our client is committed to fostering a safe and collaborative work environment in Paarl, Western Cape , and encourages employee growth and contribution.
• This role provides a stable and rewarding career path within the pharmaceutical industry.