Regulatory Affairs is now a career path in pharma, biotech, medical device and health companies. As products go through development, approval, registration, manufacturing, launch and post‑market stages companies need people who can grasp rules and keep documents and submissions compliant.
This makes Regulatory Affairs an attractive non‑clinical health career in India for people from pharmacy, medicine, dentistry, life sciences, biotech and similar fields.
Which companies are actually hiring?
Jobslly shows openings at companies like Pfizer, Masimo, ClinChoice, Cencora, Genpact, Baxter and Bristol Myers Squibb. Roles vary from Regulatory CMC and publishing to medical‑device filings, regulatory operations and intelligence.
This guide explores the companies hiring Regulatory Affairs in India, the positions they are hiring for, what these professionals may do, salary ranges and how healthcare graduates can prepare themselves for these careers.
What Does a Regulatory Affairs Professional Do?
Regulatory Affairs professionals act as a bridge between health companies and regulatory authorities.
Regulatory Affairs work can begin before a product reaches the market and continue throughout its lifecycle. Depending on the organization and specialization responsibilities may include:
- Preparing and reviewing submissions
- Supporting product registrations and renewals
- Maintaining dossiers
- Working with CTD/eCTD documentation
- Tracking changes
- Responding to health‑authority queries
- Reviewing product labels and artwork
- Supporting post‑approval changes
- Coordinating with quality, manufacturing, medical and commercial teams
- Maintaining databases and systems
- Supporting intelligence activities
- Ensuring submissions meet timelines and requirements
The exact responsibilities depend heavily on the type of company. A pharmaceutical Regulatory Affairs professional may work extensively on drug dossiers and CMC documentation while a medical‑device Regulatory Affairs professional may focus on files, registrations, ISO requirements and device‑specific regulations.
Top Companies Hiring Regulatory Affairs Professionals in India
Knowing which companies hire is only one part of the job search. Finding suitable vacancies at the right experience level can be equally difficult.
Jobslly is a healthcare-focused job platform where candidates can search opportunities across non-clinical healthcare functions, including Regulatory Affairs. Its listings currently include roles across cities such as Bengaluru, Hyderabad, Chennai, Gurgaon, Noida, and other locations.
Candidates can search using terms such as:
- Regulatory affairs
- Regulatory affairs associate
- Regulatory operations
- Regulatory publishing
- Regulatory specialist
- Regulatory CMC
- Regulatory intelligence
- Regulatory submissions
- Medical device regulatory affairs
- CMC Regulatory affairs
A targeted search can make it easier to identify opportunities that align with a candidate's degree, experience, location, and desired specialization.
The following opportunities are based on regulatory‑related listings on Jobslly during September 2026. Candidates should always verify the vacancy eligibility criteria and application status before applying.
Some of the top companies hiring for regulatory affairs role are as follows:
1. Pfizer – Associate I, Regulatory CMC Strategy
Location: Chennai
Position: Associate I, Regulatory CMC Strategy
Experience: 0–1 year of experience in Regulatory affairs within a pharmaceutical organization.
Salary: Approximately ₹4–9 LPA
Pfizer is hiring for an Associate I position within its Regulatory CMC Strategy function. The role supports activities related to license renewals and annual reports.
What does the role involve?
Regulatory Affairs professional may be responsible for:
- Supporting regulatory activities for assigned renewals and annual reports
- Preparing or compiling CMC sections
- Reviewing and supporting documentation
- Coordinating with supply and cross‑functional teams
- Applying guidelines to documentation
- Updating dossiers
- Identifying risks or timeline delays
- Reviewing stability‑related information
- Supporting post‑approval change documentation
- Ensuring submissions follow procedures
The listing specifically mentions a postgraduate degree in Pharmacy or Science and 0–1 year of Regulatory Affairs experience making this particularly relevant to candidates looking for an early‑career Regulatory Affairs opportunity.
This role demonstrates that Regulatory Affairs is not limited to professionals. Certain specialized positions can provide an entry point for candidates who already have the required foundation and can demonstrate regulatory knowledge.
2. Masimo – Regulatory Affairs Specialist
Location: Bangalore
Position: Regulatory Affairs Specialist
Experience: Around 2 years of experience in a medical device Class II or III setting.
Salary: Approximately ₹5–8 LPA
Masimos opportunity provides an example of Regulatory Affairs within the medical‑device industry than traditional pharmaceuticals.
Responsibilities include:
- Supporting filings and registrations in India
- Organizing technical files
- Maintaining product registrations
- Preparing regulatory submissions
- Supporting responses to tenders and audits
- Monitoring changes
- Communicating with regulatory teams
- Coordinating meetings
- Working with engineering, marketing and other departments
The role also highlights knowledge of regulatory requirements and ISO 13485 demonstrating how specialization can become important in medical‑device Regulatory Affairs.
Career takeaway:
Candidates interested in devices should not restrict their job searches to pharmaceutical Regulatory Affairs titles. Device registration, quality, compliance, post‑market surveillance and regulatory operations can all provide routes into the regulatory ecosystem.
3. ClinChoice – Senior Associate, Regulatory Affairs
Location: Bangalore
Position: Senior Associate – Regulatory Affairs
Salary: Approximately ₹10.1–11 LPA
Jobslly currently lists a Senior Associate – Regulatory Affairs position with ClinChoice in Bangalore. The role is described as supporting regulatory submissions within a global pharmaceutical environment.
The position is particularly relevant to candidates in regulatory publishing and electronic submissions.
Potential responsibilities include:
- Preparing regulatory submissions
- Supporting regulatory publishing activities
- Organizing submission documents
- Checking documents for completeness and consistency
- Working with documentation
- Supporting submission timelines
- Coordinating with cross‑functional teams
This highlights another important Regulatory Affairs specialization: regulatory operations and publishing.
Professionals who develop document‑management, technical writing, electronic submission and quality‑checking skills can potentially build careers in this area.
4. Cencora – Senior Specialist, Regulatory Affairs CMC Biologics
Location: Noida
Position: Senior Specialist, Regulatory Affairs – CMC, Biologics
Salary: Approximately ₹6–12.4 LPA
Cencora has a Regulatory Affairs opportunity focused on CMC and biologics. CMC stands for Chemistry, Manufacturing and Controls. Represents a specialized area of regulatory work involving the quality and manufacturing aspects of pharmaceutical products.
What could Regulatory Affairs professionals work on?
- Managing regulatory tasks
- Supporting projects
- Coordinating client stakeholders
- Maintaining high documentation accuracy
- Supporting deliverables
- Communicating with teams
- Guiding colleagues and smaller projects
This is an example of how Regulatory Affairs careers can branch into specialist domains such as biologics, CMC, regulatory strategy and global submissions.
5. Genpact – Regulatory Affairs Operations Specialist
Location: Gurgaon
Position: Regulatory Affairs Operations Specialist – 4B
Salary: Approximately ₹5–10.2 LPA
Genpacts listing represents a different side of regulatory work: regulatory operations and reporting.
The role involves supporting regulatory reporting collecting and validating data from different systems monitoring regulatory changes and maintaining accurate reporting.
Key responsibilities include:
- Collecting data from systems
- Checking data accuracy
- Supporting reporting
- Identifying data issues
- Monitoring changes
- Updating reporting templates
- Maintaining change records
- Supporting compliance‑related activities
The listing accepts backgrounds including Pharmacy, Healthcare and Health Administration while a Masters in Public Health or Regulatory Affairs is also considered.
Career takeaway:
Regulatory Affairs is not about preparing drug‑registration dossiers. Professionals with analytical, documentation, reporting and communication skills can also explore regulatory operations.
6. Baxter – RA Senior Specialist
Location: Gurgaon
Position: RA Senior Specialist – Regulatory Affairs
Salary: Approximately ₹11.4–16.3 LPA
Experience: 5 years of relevant experience
Baxters listing focuses on activities for pharmaceutical and medical‑device products across India with additional work involving Bangladesh and Sri Lanka.
Responsibilities include:
- Managing product registrations
- Handling renewals and variations
- Preparing dossiers
- Coordinating with health authorities
- Using systems such as SUGAM
- Reviewing labels and artwork
- Assessing manufacturing and product changes
- Supporting audits and inspections
- Working with distributors and regulatory partners
- Collaborating with quality supply chain, commercial and global regulatory teams
The position asks for at least five years of relevant experience illustrating the earning potential that can develop as Regulatory Affairs professionals progress into senior roles.
7. Bristol Myers Squibb – Regulatory Specialist
Location: Hyderabad
Position: Regulatory Specialist, Portfolio Acceleration and Analytics
Salary: Approximately ₹7.5–15 LPA
Bristol Myers Squibb has a Regulatory Affairs specialist opportunity focused on operations, submissions, documentation, regulatory intelligence, analytics and compliance.
Responsibilities include:
- Managing documentation
- Updating document metadata
- Supporting health‑authority responses
- Maintaining dashboards
- Supporting regulatory analytics
- Contributing to technology and process‑improvement projects
- Supporting intelligence activities
This role demonstrates how technology and data are increasingly becoming part of modern Regulatory Affairs.
Professionals who combine knowledge with digital documentation, analytics, communication and process‑management skills can create a stronger profile for these evolving roles.
What Skills Do Employers Look for in Regulatory Affairs?
A healthcare degree alone may provide knowledge but industry employers often expect candidates to understand how that knowledge is applied within a regulated environment.
1. Regulatory knowledge
Candidates should understand authorities, pharmaceutical regulations, submission pathways and compliance requirements.
2. CTD and eCTD knowledge
Understanding how regulatory information is organized and submitted is essential, for Regulatory Affairs professionals.
3. Scientific and regulatory writing
Regulatory Affairs professionals frequently work with structured documents. Clear accurate concise writing is therefore vital.
4. Documentation and attention to detail
An error in a document can ruin a submission. Employers value professionals who check information carefully and keep track of versions.
5. Communication
Regulatory Affairs professionals talk with authorities and with internal teams such as Quality, Clinical, Medical, Manufacturing, Supply Chain and R&D.
6. Regulatory intelligence
Regulatory Affairs professionals must watch for changes in regulations. Know how those changes can impact products or submissions.
7. Project management
When many submissions have deadlines Regulatory Affairs professionals must decide priorities coordinate tasks and manage timelines.
How Can Healthcare Professionals Enter Regulatory Affairs?
Candidates from BPharm, MPharm, PharmD, MBBS, BDS, biotechnology, life sciences and similar backgrounds already have a science base. The challenge is turning that knowledge into industry‑ready regulatory skills.
Structured upskilling can help.
Academically offers Non-Clinical Courses for Healthcare Professionals that help healthcare graduates move toward industry jobs. The programmes cover areas such as Medical Affairs, Clinical Drug Development, Pharmacovigilance, Medical Writing, Clinical Research, HEOR and Clinical Data Management.
The value of training is not just the certificate. Candidates must show that they can translate healthcare knowledge into industry workflows.
Academically’s programmes can help candidates build:
- Industry‑oriented knowledge
- Understanding of healthcare processes
- Scientific communication skills
- Project exposure
- Knowledge relevant to development and regulatory submissions
- Resume‑building support
- Profile optimisation
- Mock interview preparation
- Job assistance through Jobslly
Academically also states that successful completion of its non‑clinical programmes gives 180 CPD points valid for five years.
For candidates who want Regulatory Affairs programmes that cover drug development, medical affairs, medical writing and similar industry functions give useful adjacent knowledge because Regulatory Affairs work often overlaps with clinical scientific, medical and documentation activities.
Regulatory Affairs Career Path in India
Regulatory Affairs can offer many progress routes.
A candidate may start as:
Healthcare degree→Upskill with academically's non-clinical course→ Regulatory Affairs Trainee → Regulatory Affairs Associate → Regulatory Affairs Specialist → Senior Regulatory Affairs Specialist → Regulatory Affairs Manager → Senior Manager/Director
Specialisation can also lead to:
- Regulatory CMC
- Regulatory Operations
- Regulatory Publishing
- Regulatory Strategy
- Regulatory Intelligence
- Medical Device Regulatory Affairs
- Global Regulatory Affairs
- Post‑Approval Regulatory Affairs
- Labeling
- Submission Management
The right pathway depends on education, company, geography, therapeutic area and experience.
Final Takeaway
The current landscape of companies hiring Regulatory Affairs in India shows that Regulatory Affairs is wider than traditional pharmaceutical registration work.
Pfizer offers exposure to Regulatory CMC strategy, Masimo shows opportunities in devices, ClinChoice highlights regulatory publishing, Cencora focuses on biologics CMC, Genpact demonstrates regulatory operations, Baxter covers product registration and lifecycle management and Bristol Myers Squibb mixes regulatory operations with analytics and intelligence.
The important lesson, for aspiring professionals is that a healthcare degree is a starting point, not the full industry skill set. Candidates who add knowledge, documentation skills, scientific communication, submission awareness and practical exposure can build a stronger profile.
For healthcare professionals who want to move from purely clinical work Academically’s non‑clinical programmes can give structured industry‑oriented upskilling while Jobslly can help them discover relevant healthcare job opportunities.
The strongest strategy is simple: choose a Regulatory Affairs specialization, build the skills, create an industry‑focused resume, gain practical exposure and consistently monitor relevant vacancies.
