Assistant Manager Quality Assurance – Validation

About the role

CCL Pharmaceuticals is seeking an Assistant Manager to lead validation and quality assurance activities at its Sundar Plant. You will work closely with Quality Control, Production, Engineering and cross‑functional teams to ensure compliance with GMP, regulatory expectations and internal standards.

Key responsibilities

• Prepare, execute and document validation protocols for analytical methods, manufacturing processes, cleaning procedures, hold‑time studies, CS‑validation and equipment qualification.
• Conduct validation and qualification activities in line with approved procedures and GMP requirements.
• Compile validation reports and supporting documentation for regulatory compliance.
• Support analytical method validation, comparative dissolution studies, equipment qualification and environmental monitoring in the QC laboratory.
• Collaborate with stakeholders to drive continuous improvement across quality systems.

Required profile

• Pharm‑D, BSc/MSc Chemistry or equivalent qualification.
• 4–6 years of Quality Assurance experience in the pharmaceutical industry.
• Hands‑on experience with process, cleaning, analytical method and computerized system validation, as well as equipment qualification.
• Strong understanding of GMP, quality systems and regulatory requirements.

Required skills

• Process validation
• Cleaning validation
• Analytical method validation
• Computerized System Validation (CSV)
• Equipment qualification
• GMP compliance
• Quality systems knowledge
• Regulatory requirements interpretation

What we offer

• Collaborative, mission‑driven environment
• Opportunities for learning, leadership and innovation
• Contribution to global health impact