Quality Control Analyst

Placements24; George; On-site; ZAR 360,000 - 480,000; Full time

Benefits offered by this job

Competitive salary

Health benefits

Training & growth

Stable work in George

Retirement plan

Job summary

Placements24 is seeking a diligent Quality Control Analyst to join a pharmaceutical manufacturing facility in George. You will conduct a wide range of laboratory tests to ensure quality and safety of products, leveraging HPLC and dissolution testing while upholding stringent regulatory standards.

The role requires a Bachelor's degree in a related field and 2-3 years' QC experience, with strong analytical skills and meticulous attention to detail.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
• 2-3 years of experience as a QC Analyst in the pharmaceutical industry preferred.
• Hands-on experience with HPLC and dissolution testing essential.
• Knowledge of cGMP, quality systems, and laboratory safety procedures.
• Strong analytical and problem-solving skills, with meticulous attention to detail.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.

Responsibilities

• Perform routine testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical methods.
• Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Accurately record and document all test results, observations, and deviations in accordance with cGMP and company SOPs.
• Analyze data, interpret results, and report any out-of-specification findings to the Quality Unit promptly.
• Prepare reagents, standards, and solutions required for testing.
• Participate in method validation, transfer, and qualification activities as needed.

Skills

Analytical thinking

Attention to detail

Teamwork

Independent work

Education

Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or related field

Tools

HPLC

Dissolution testing

Job description

About the Role

Our client is seeking a diligent and detail-oriented Quality Control Analyst to join their pharmaceutical manufacturing facility in George . You will play a crucial role in ensuring the quality and safety of our pharmaceutical products by conducting a wide range of laboratory tests. This position requires a strong understanding of analytical techniques and a commitment to upholding stringent quality standards. You will work closely with the quality assurance team to maintain compliance with regulatory requirements and contribute to the continuous improvement of our quality systems. This is an excellent opportunity for an individual passionate about pharmaceutical quality and accuracy, working in a well-established company with a commitment to excellence.

Key Responsibilities

• Perform routine testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical methods.
• Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Accurately record and document all test results, observations, and deviations in accordance with cGMP and company SOPs.
• Analyze data, interpret results, and report any out-of-specification findings to the Quality Unit promptly.
• Prepare reagents, standards, and solutions required for testing.
• Participate in method validation, transfer, and qualification activities as needed.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
• 2-3 years of experience as a QC Analyst in the pharmaceutical industry is preferred.
• Hands-on experience with HPLC and dissolution testing is essential.
• Knowledge of cGMP, quality systems, and laboratory safety procedures.
• Strong analytical and problem-solving skills, with meticulous attention to detail.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.

Benefits

• Competitive annual salary.
• Comprehensive health and retirement benefits.
• Paid training and opportunities for professional growth.
• A stable and supportive work environment in George .
• Contribution to the manufacturing of essential medicines.