Ceph Lifesciences Pvt Ltd, a growing player in the pharmaceutical industry with operations across India (including facilities in Himachal Pradesh and registered base in Telangana), is actively expanding its Quality Assurance (QA) team. The company is inviting applications for several exciting positions in Quality Management System (QMS) and Validation departments.
If you have experience in pharmaceutical quality compliance, validation processes, or quality systems in a regulated environment, this is a great opportunity to join a dynamic organization focused on quality excellence and manufacturing of high-quality pharma products.
These roles are ideal for professionals passionate about ensuring regulatory compliance, process validation, and maintaining the highest standards in pharmaceutical operations.
Open Positions Ceph Lifesciences is recruiting for the following roles in its QA team:
- Assistant Manager
- QMS Senior Officer
- QMS Officer
- Validation Executive
- Validation Officer / Senior Officers
These positions involve working on quality systems, validation activities, documentation, audits, and compliance in a pharma manufacturing setup.
Roles and Responsibilities Selected candidates will be responsible for:
- Overseeing and implementing Quality Management Systems (QMS) as per regulatory guidelines (GMP, WHO, etc.)
- Conducting process, equipment, and cleaning validation activities
- Preparing, reviewing, and approving validation protocols and reports
- Handling deviations, CAPA (Corrective and Preventive Actions), and change controls
- Participating in internal audits, regulatory inspections, and quality risk assessments
- Ensuring documentation compliance and training team members on quality procedures
- Supporting continuous improvement initiatives in quality assurance
Required Qualifications and Skills Candidates should meet the following criteria:
- Educational background: B.Pharm / M.Pharm / MSc (Microbiology / Biotechnology / Chemistry) or equivalent
- Relevant experience: 2–10+ years in QA/QC/Validation/QMS in pharmaceutical industry (experience varies by role level)
- Strong knowledge of GMP, GLP, USFDA/EDQM/WHO guidelines, and validation principles
- Proficiency in documentation, data analysis, and quality tools
- Excellent communication, attention to detail, and problem-solving skills
- Experience with QMS software/tools and regulatory audits is a plus
Salary and Benefits Salary is competitive and commensurate with experience and role level. Realistic range for these positions in the Indian pharma sector (Himachal Pradesh/Telangana operations): ₹3.5 LPA to ₹8 LPA (higher for senior/manager roles).
Additional benefits typically include:
- Health insurance
- Performance-based incentives
- Professional development opportunities
- Statutory benefits (PF, ESI, gratuity, etc.)
How to Apply Interested candidates can send their updated CV/resume immediately.
- Contact Number: 9317911968 (for queries or submission)
- Email: hr.unit6@neclife.com (preferred for CV submission)
Apply promptly with your CV, mentioning the position applied for in the subject line. Shortlisted candidates will be contacted for further rounds.
