Regulatory Affairs Executive Vacancies at Piramal Pharma
- Executive Regulatory Affairs vacancies at Piramal, Navi Mumbai.
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Equal Employment Opportunity
- Application Process
- Frequently Asked Questions
- Is this role suitable for freshers?
- What department does this role belong to?
- Is this a full-time role?
- What skills are important for Regulatory Affairs roles?
- Are there growth opportunities?
Executive Regulatory Affairs vacancies at Piramal, Navi Mumbai.
Regulatory Affairs continues to be one of the most stable and high-growth career paths within the pharmaceutical and life sciences industry. Piramal Group is currently hiring an Executive – Regulatory Affairs at its Navi Mumbai facility. This opportunity is well suited for chemistry graduates who want to build long-term careers in pharma compliance, quality systems, and regulated manufacturing environments while working with a globally respected organization.
Company Overview
Piramal Group is one of India’s most respected diversified business conglomerates with a strong presence in pharmaceuticals, healthcare, and life sciences. Over the past three decades, the group has grown through a balanced strategy of organic expansion and strategic acquisitions, establishing itself as a trusted global partner across regulated markets.
Piramal Pharma Solutions operates as a Contract Development and Manufacturing Organization offering end-to-end services across the drug lifecycle. The company supports global innovators and generic manufacturers with capabilities spanning drug discovery, pharmaceutical development, clinical trial supplies, commercial API manufacturing, finished dosage forms, and advanced biologics.
With manufacturing and development facilities across North America, Europe, and Asia, Piramal maintains strict compliance with global regulatory standards. The organization is widely recognized for its ethical governance, scientific depth, and long-term commitment to healthcare advancement.
Job Role & Responsibilities
The Executive – Regulatory Affairs role is a full-time position within the Regulatory Affairs department. The role supports compliance activities, documentation control, laboratory systems, and investigation handling in a regulated pharmaceutical environment.
Key responsibilities include:
• Preparation, review, and updating of SOPs, specifications, methods of analysis, reports, and protocols • Review of IQ, OQ, and PQ documentation for new laboratory instruments • Coordination with authorized vendors and suppliers for QC instrument troubleshooting and technical support • Execution and maintenance of calibration and validation schedules for QC instruments • Ensuring compliance with Good Laboratory Practices across QC operations • Handling change control documentation and regulatory records within the QC department • Monitoring laboratory management procedures to ensure SOP adherence • Participation in investigations related to deviations, OOS, and OOT • Supporting departmental operations and assuming reporting authority responsibilities when required
This role provides hands-on exposure to regulatory documentation, quality systems, and compliance-driven pharmaceutical manufacturing processes.
Eligibility / Qualifications
The position is open to candidates with a strong academic background in chemistry or related disciplines who are interested in regulatory and compliance-focused pharma roles.
Required qualifications:
• Bachelor’s or Master’s degree in Chemistry or a related scientific field • Basic understanding of pharmaceutical regulatory requirements and quality systems • Familiarity with laboratory documentation and SOP-based working environments • Strong attention to detail and commitment to data integrity • Ability to work collaboratively within cross-functional teams • Good written and verbal communication skills • Willingness to learn regulatory frameworks and adapt to evolving compliance requirements
Preferred education background includes: BSc Chemistry, MSc Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, Organic Chemistry, Industrial Chemistry
Knowledge of peptide synthesis principles or exposure to regulated manufacturing environments will be considered an added advantage.
Location & Salary
Job Location: Navi Mumbai, Maharashtra
The role is based at Piramal’s regulated manufacturing and development facility in Navi Mumbai. Salary details are not publicly disclosed; however, Piramal Pharma Solutions offers competitive compensation aligned with industry standards for regulatory affairs jobs in India.
Additional benefits typically include:
• Performance-linked salary growth • Structured learning and career progression • Exposure to global regulatory audits and inspections • Employee wellness and benefits programs • Stable long-term employment in a regulated pharma environment
Equal Employment Opportunity
Piramal Group is an Equal Employment Opportunity employer committed to inclusive growth and ethical employment practices. All employment decisions are based strictly on merit, qualifications, skills, and performance. The organization provides equal opportunity across recruitment, training, promotion, compensation, and workplace practices.
Application Process
Eligible candidates can apply online through the official Piramal careers portal using the link below:
Apply Online: https://hcwf.fa.ap1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1005/job/10236?utm_medium=jobshare
Shortlisted candidates will be contacted by the recruitment team for further evaluation and interview rounds.
Frequently Asked Questions
Is this role suitable for freshers?
Candidates with strong academic backgrounds and basic regulatory knowledge can apply. Prior pharma experience is beneficial but not mandatory.
What department does this role belong to?
The position is part of the Regulatory Affairs department supporting QC and laboratory compliance activities.
Is this a full-time role?
Yes. This is a full-time position with long-term growth potential.
What skills are important for Regulatory Affairs roles?
Attention to detail, documentation accuracy, regulatory awareness, and strong communication skills are critical.
Are there growth opportunities?
Yes. Regulatory Affairs offers stable career progression into senior RA, compliance, and quality leadership roles.
| Category | Details |
|---|---|
| Company | Piramal Pharma Solutions |
| Vacancies | Executive – Regulatory Affairs |
| Required Education | BSc Chemistry, MSc Chemistry, Pharmaceutical Chemistry |
| Experience | Entry-level to Experienced |
To apply for this job please visit hcwf.fa.ap1.oraclecloud.com.
