Description:
We are a leading pharmaceutical company committed to delivering high-quality products to our customers. We are currently seeking a skilled and experienced Quality Control Manager to join our team and help maintain our high standards of excellence.
Key Responsibilities:
- Oversee the daily operations of the Quality Control (QC) laboratory, ensuring all processes are in compliance with cGMP, GLP, and international pharmaceutical standards.
- Manage, mentor, and lead the QC team to achieve departmental goals and maintain a high standard of testing and analysis.
- Coordinate and ensure the proper execution of internal and vendor audits.
- Ensure all laboratory equipment is maintained, calibrated, and compliant with regulations.
- Prepare, review, and maintain QC documentation and reports in accordance with regulatory requirements.
- Collaborate with other departments to ensure the continuous improvement of quality processes.
Why Join Us:
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and collaborative work environment.
If you are a highly skilled QC professional with a passion for excellence in pharmaceutical standards, we would love to hear from you.
To Apply:
Please send your CV and cover letter to chriszelle.steyn@mspmedical.co.za .
Requirements:
- Oversee the daily operations of the Quality Control (QC) laboratory, ensuring all processes are in compliance with cGMP, GLP, and international pharmaceutical standards.
- Manage, mentor, and lead the QC team to achieve departmental goals and maintain a high standard of testing and analysis.
- Coordinate and ensure the proper execution of internal and vendor audits.
- Ensure all laboratory equipment is maintained, calibrated, and compliant with regulations.
- Prepare, review, and maintain QC documentation and reports in accordance with regulatory requirements.
- Collaborate with other departments to ensure the continuous improvement of quality processes.
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and collaborative work environment.
- Laboratiry Management: 4 to 5 years
- Education: Master’s degree in Chemistry, Analytical Chemistry, Biochemistry, or a relevant scientific field (PhD in Chemistry preferred).
- Experience:
- At least 5 years of laboratory experience, with at least 3 years of QC lab management experience in a pharmaceutical or similar regulated environment.
- Hands-on experience with internal and vendor audits is an advantage.
- Technical Skills:
- Proficient in MS Office, SAP, and LIMS (Laboratory Information Management System).
- Strong understanding of cGMP, GLP, and international pharmaceutical standards.
- Additional Skills:
- Strong leadership and team management abilities.
- Excellent attention to detail and organizational skills.
- Ability to troubleshoot issues and provide effective solutions in a high-pressure environment.
- At least 5 years of laboratory experience, with at least 3 years of QC lab management experience in a pharmaceutical or similar regulated environment.
- Hands-on experience with internal and vendor audits is an advantage.
- Proficient in MS Office, SAP, and LIMS (Laboratory Information Management System).
- Strong understanding of cGMP, GLP, and international pharmaceutical standards.
- Strong leadership and team management abilities.
- Excellent attention to detail and organizational skills.
- Ability to troubleshoot issues and provide effective solutions in a high-pressure environment.
Key Requirements:
- Education: Master’s degree in Chemistry, Analytical Chemistry, Biochemistry, or a relevant scientific field (PhD in Chemistry preferred).
- Experience:
- At least 5 years of laboratory experience, with at least 3 years of QC lab management experience in a pharmaceutical or similar regulated environment.
- Hands-on experience with internal and vendor audits is an advantage.
- Technical Skills:
- Proficient in MS Office, SAP, and LIMS (Laboratory Information Management System).
- Strong understanding of cGMP, GLP, and international pharmaceutical standards.
- Additional Skills:
- Strong leadership and team management abilities.
- Excellent attention to detail and organizational skills.
- Ability to troubleshoot issues and provide effective solutions in a high-pressure environment.
06 Mar 2025;
from:
careers24.com