Cipla Team Member Qms & Compliance Recruitment
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Experience Requirement
- Core Competencies
- Eligible Courses (Comma-Separated)
- Location & Salary
- Job Location
- Employment Type
- Salary Information
- How to Apply
- FAQs
- Who can apply for the Team Member – QMS & Compliance role?
- Is experience in formulations mandatory?
- Does this role involve audit exposure?
- Where is the job located?
- How do I apply?
- Summary Table
Cipla is hiring for the Team Member – QMS & Compliance position at its Rangpo manufacturing site in Sikkim, India. This vacancy is part of the Quality Assurance and Quality Management Systems function and is designed for professionals with prior exposure to pharmaceutical QA and compliance operations. The role supports site-level quality systems, batch documentation review, deviation handling, CAPA management, and audit readiness activities. This opportunity is well suited for experienced professionals seeking stable growth in regulated pharmaceutical manufacturing environments in Sikkim.
Company Overview
Cipla is one of India’s most respected global pharmaceutical companies with a strong legacy in quality-driven manufacturing, regulatory compliance, and affordable healthcare solutions. With operations across multiple countries and approvals from global regulatory agencies, Cipla continues to play a critical role in advancing public health through high-quality formulations and innovative therapies.
The Rangpo facility in Sikkim is a key manufacturing location supporting regulated markets. The site operates under strict quality systems aligned with national and international regulatory requirements. Cipla’s commitment to robust Quality Management Systems, continuous improvement, and ethical manufacturing makes it a preferred employer for quality professionals seeking long-term career stability and professional credibility.
Job Role & Responsibilities
The Team Member – QMS & Compliance role supports the implementation, maintenance, and continuous improvement of quality systems at the site level. The position involves close collaboration with QA, production, supply chain, and regulatory teams to ensure consistent compliance with current Good Manufacturing Practices.
Key Responsibilities
- Reviewing batch manufacturing records to ensure completeness, accuracy, and compliance with approved SOPs
- Supporting deviation documentation, change control processes, and CAPA tracking activities
- Participating in root cause analysis and monitoring timely CAPA closure
- Maintaining audit trail documentation and supporting internal and external audit preparation
- Assisting in the timely closure of audit observations and regulatory commitments
- Maintaining and updating QMS documentation including SOPs, APQRs, and quality agreements
- Participating in GxP training programs and monitoring adherence to compliance standards
- Supporting implementation of DCGI notifications and regulatory updates
- Contributing to site-level risk assessment activities and mitigation planning
- Assisting in product evaluation activities and recall coordination under supervision
- Coordinating with cross-functional teams to ensure alignment on quality actions
This role contributes directly to audit readiness, regulatory compliance, and the prevention of quality incidents and product recalls.
Eligibility / Qualifications
Educational Qualification
- B.Pharm or M.Pharm
Experience Requirement
- 2–5 years of relevant experience in pharmaceutical QA or QMS roles
- Prior exposure to formulations or microbiology environments preferred
Core Competencies
- Strong understanding of pharmaceutical quality systems
- Knowledge of deviation management, CAPA processes, and batch record review
- Ability to manage documentation accurately in a fast-paced environment
- Effective coordination and communication skills across departments
- Structured approach to compliance and continuous improvement
Eligible Courses (Comma-Separated)
B.Pharm, M.Pharm, MSc Pharmaceutical Sciences, MSc Microbiology, MSc Biotechnology
Location & Salary
Job Location
Rangpo, Sikkim, India
Employment Type
Full-time
Salary Information
Compensation will be offered as per company norms and will depend on qualifications, experience, and internal role evaluation. The role provides strong exposure to regulated manufacturing operations, audit-facing responsibilities, and site-level quality governance.
How to Apply
Apply online using the link below:
Candidates are encouraged to apply early, as shortlisting is conducted on an ongoing basis.
FAQs
Who can apply for the Team Member – QMS & Compliance role?
Candidates with a B.Pharm or M.Pharm degree and 2–5 years of experience in pharmaceutical QA or QMS roles can apply.
Is experience in formulations mandatory?
Experience in formulations or microbiology environments is preferred but not mandatory.
Does this role involve audit exposure?
Yes. The role actively supports internal audits, external inspections, and regulatory readiness activities.
Where is the job located?
The position is based at Cipla’s Rangpo facility in Sikkim.
How do I apply?
Applications must be submitted through the official Cipla careers portal link provided above.
Summary Table
| Company | Cipla |
|---|---|
| Vacancies | Team Member – QMS & Compliance |
| Required Education | B.Pharm, M.Pharm, MSc Pharmaceutical Sciences, MSc Microbiology |
| Experience | 2–5 Years |
To apply for this job please visit careers.cipla.com.
