Executive Regulatory Affairs Jobs at Piramal Pharma in Navi Mumbai at Piramal Pharma Solutions for chemistry graduates seeking regulatory and quality compliance careers.
Company Overview
Piramal Pharma Solutions (PPS), a part of the globally respected Piramal Group, is a leading Contract Development and Manufacturing Organization (CDMO) offering integrated solutions across the pharmaceutical product lifecycle. With operations spanning North America, Europe, and Asia, PPS supports innovators and generic manufacturers through advanced development, manufacturing, and regulatory-compliant services. Executive Regulatory Affairs Jobs
With decades of experience and a strong foundation built on ethics, quality, and innovation, Piramal continues to invest in people, technology, and global capabilities. To strengthen its regulatory and quality-driven operations, the company is inviting qualified professionals to join its Regulatory Affairs team in Navi Mumbai. Executive Regulatory Affairs Jobs
Job Location & Employment Type
- Job Location: Navi Mumbai (Thane), Maharashtra
- Employment Type: Full-time
- Work Mode: On-site
- Department: Regulatory Affairs
- Business Unit: PPL (Piramal Pharma Limited)
- Travel Requirement: Low
Open Positions / Department Details
- Position Title: Executive – Regulatory Affairs
- Job Category: Regulatory Affairs
- Job Identification Number: 10236
- Reporting Function: Regulatory Affairs & Quality Operations
This position supports regulatory and laboratory compliance activities within a highly regulated pharmaceutical manufacturing and development environment. Executive Regulatory Affairs Jobs
Key Roles & Responsibilities
The Executive – Regulatory Affairs will play a vital role in maintaining regulatory compliance, supporting quality systems, and ensuring laboratory practices meet global standards. Key responsibilities include: Executive Regulatory Affairs Jobs
- Preparation, review, and periodic updating of SOPs, specifications, analytical methods, protocols, and technical reports
- Reviewing and supporting qualification activities such as IQ, OQ, and PQ for new laboratory instruments
- Coordinating troubleshooting activities for QC instruments and liaising with authorized service providers when required
- Planning, executing, and maintaining calibration and validation schedules for all QC laboratory instruments
- Ensuring strict adherence to Good Laboratory Practices (GLP) within the Quality Control function
- Managing change control documentation and ensuring compliance with internal procedures
- Monitoring laboratory management activities to ensure SOP compliance
- Participating in investigations related to deviations, OOS (Out of Specification), and OOT (Out of Trend)
- Supporting departmental operations and handling responsibilities in the absence of the reporting manager
- Assisting in continuous improvement initiatives and compliance-related activities as assigned by senior leadership
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in:
- Chemistry
- Pharmaceutical Sciences
- Or other closely related scientific disciplines
Experience
- Experience requirements are not explicitly stated; however, candidates with prior exposure to regulatory affairs, QC, or laboratory compliance will be preferred.
Skills Required
- Strong understanding of quality systems and regulatory documentation
- Familiarity with laboratory compliance, validation, and calibration processes
- Exposure to deviation, OOS, and OOT investigations
- Basic understanding of peptide synthesis principles is an added advantage
- High attention to detail with a quality-focused mindset
- Ability to work collaboratively in cross-functional teams
- Good verbal and written communication skills
- Willingness to learn, adapt, and handle additional responsibilities
- Ability to work independently during critical operational situations
Executive Regulatory Affairs Jobs
Salary & Benefits
- Salary: As per company norms
Additional benefits include:
- Opportunity to work with a globally recognized pharmaceutical group
- Exposure to advanced regulatory and laboratory compliance systems
- Structured career growth within a regulated environment
- Inclusive and ethical workplace culture
- Equal opportunity employment with merit-based progression
Executive Regulatory Affairs Jobs
Selection Process
The selection process may include:
- Application screening based on qualifications and experience
- Technical interview focusing on regulatory affairs and quality systems
- HR or final discussion
The exact hiring process may vary depending on business needs.
How to Apply
- Mode of Application: Online Application Only
Interested candidates should apply through the official Piramal careers portal using the job identification number mentioned above. No walk-in or direct email applications are specified for this role. Executive Regulatory Affairs Jobs
Important Dates
- Application Deadline: Not specified (early application recommended)
Why Apply for This Pharma Job?
This role is an excellent opportunity for professionals seeking hands-on exposure to regulatory affairs within a global CDMO environment. Working at Piramal Pharma Solutions allows candidates to build strong expertise in quality systems, regulatory compliance, and laboratory governance while being part of an organization known for ethical practices, innovation, and long-term growth. Executive Regulatory Affairs Jobs
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical job information platform and is not affiliated with Piramal Pharma Solutions or Piramal Group. All job details are shared for informational purposes only. Candidates are advised to apply through official company channels and verify information directly from the employer. Executive Regulatory Affairs Jobs
Final Call-to-Action
If you have a background in chemistry or pharmaceutical sciences and are looking to grow your career in regulatory affairs within a global organization, apply now and take the next step in your professional journey. Executive Regulatory Affairs Jobs
