Assistant Quality Control Manager

Job Title: Assistant Quality Control Manager

Department: Quality Control

Reporting to: Quality Control Manager / Plant Manager

Location: Kamion Pharma, Plot No. G-4/C, SITE, Super Highway Phase 2, Karachi, Pakistan

Job Summary:

The Assistant QC Manager will support the QC Manager in overseeing all quality control operations. This role ensures that raw materials, in-process materials, and finished products meet regulatory and company standards. The Assistant QC Manager will supervise QC staff, monitor testing processes, and help maintain compliance with ISO 13485, DRAP regulations, and GMP standards.

Key Responsibilities:

1. Assist the QC Manager in supervising and guiding QC officers, technicians, and junior staff to ensure smooth daily operations.
2. Oversee and participate in inspection and testing of raw materials, packaging materials, in process samples, and finished products.
3. Ensure compliance with ISO / GMP, DRAP regulations, GLP, and other relevant standards in all QC activities.
4. Review QC lab schedules, monitor workflow, and ensure testing is completed accurately and on time.
5. Support product stability testing as per SOPs to verify the product’s shelf life, detect potential quality issues and report them promptly.
6. Maintain accurate records of all QC activities, including inspection, testing, and nonconformities.
7. Investigate quality issues or nonconformities and coordinate with other departments for timely resolution.
8. Assist in checking quality of materials from suppliers and take part in reviewing and auditing vendors.
9. Help prepare for internal and external audits, providing necessary documentation and support.
10. Gather and analyze quality data, generate reports, and recommend improvements in QC processes.

Qualifications and experience:

• Bachelor’s degree in Pharm D or Microbiology recognized by HEC.
• At least 5 years of experience in quality control / testing, preferably in a pharmaceutical or medical device manufacturing facility.

Skills:

• Able to operate HPLC equipment and stability chambers by following approved procedures.
• Able to manage multiple QC tasks efficiently and meet deadlines
• Strong attention to detail and problem-solving skills.
• Good knowledge of GMP, ISO and DRAP regulations.
• Effective communication and leadership skills and ability to work well with different teams.

Working Conditions:

• Full time, on site position at Kamion Pharma’s manufacturing facility.
• Additional working hours may be required during high production periods.

Application:
Qualified candidates should submit their resume at .

Skills:

• Able to operate HPLC equipment and stability chambers by following approved procedures.
• Able to manage multiple QC tasks efficiently and meet deadlines
• Strong attention to detail and problem-solving skills.
• Good knowledge of GMP, ISO and DRAP regulations.
• Effective communication and leadership skills and ability to work well with different teams.