Johnson & Johnson Posted July 16, 2025

Technical Product Owner - Regulatory Excellence Platform Lead

Hyderabad, India Full time
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Johnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

R&D Product Development

Job Sub Function:

R&D Software/Systems Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Hyderabad, Andhra Pradesh, India

Job Description:

Johnson & Johnson Innovative Medicine R&D IT is seeking a Technical Product Owner, Platform Lead for Unified Regulatory Platform (URP), located in Hyderabad, India. At Johnson & Johnson Innovative Medicine, we take patient safety and well-being into our core values. We bring together the best minds and pursue the most promising science.

The Platform Lead for URP will manage the URP and integration infrastructure, leading activities such as VPN setup, SSO configuration, Azure account management, and other related services to ensure secure and efficient access to the URP SaaS platform, as well as to other internal and external integrations that will be part of the URP landscape. The Platform Lead will implement standard methodologies for network security and performance while collaborating with multi-functional teams to maintain platform stability and scalability.

Additionally, the Platform Lead will help craft the platform vision and prioritize new technical features and improvements to the products on the platform to meet regulatory business needs. They will be accountable for technical delivery and value realization together with the Technical Product Manager and Business Product Owner. They will ensure that the product's technical architecture aligns with the technological roadmap and adheres to established technical engineering standards.

Key Responsibilities:

Perform end-to-end URP platform lifecycle activities including release management, delivery and performance management of the URP platform and integrations

Collaborate with J&J IM Product Owners to build a technical backlog that delivers business value while meeting the needs of supporting teams

Work in close partnership with the Regulatory architect and technology counterparts to lead cross-team dependencies in roadmaps and backlog

Work with UPR platform vendor and Product Manager regarding capacity & product requirements on the platform and lay the foundation of scalable and high performing product

Ensure platform fits into the broader Enterprise Architecture guidelines and standards (e.g., APIs, security controls, approved technologies, data standards, etc.) and maintain leading expertise on tech capabilities relevant to the platform

Drive selection of platform solutions (e.g., AWS, Azure vs Google Cloud); work with the lead engineers to assess technical elements of the product

In combination with engineering, develop high level solutions for platform features to enable product teams

Ensure and facilitate Change Control and Risk Management Processes across the URP platform and Regulatory Excellence products

Drive continuous improvement across URP platform and products through automation, measurements and standard methodologies

Implement necessary IS security, GxP and other (compliance) items

Provide support and point of escalation across all stages of the solution lifecycle including operational support and architecture optimization

Responsible for defining and communicating a shared technical and architectural vision to ensure solution is fit for its intended purpose

Qualifications

Education: Bachelor's or higher in Computer Science or similar (Engineering, Math, Physics, IT)

Experience and Skills:

Required:

A minimum of ten (10) years of relevant IT and business experience is required

Knowledge of global regulatory affairs, regulations, computer systems validation requirements, current industry regulatory technology landscape, including knowledge of vendors, systems and what is new & upcoming in this space and all vital compliance requirements for workflow, reporting, and information custody for medicinal products companies

Excellent understanding of Global Regulatory Affairs systems, processes, and system/data integrations with downstream systems

Experience leading the selection, building, and integration of platforms including Cloud Native technologies, data management, API architecture/design. Strong understanding and knowledge about cloud computing technologies and platforms

Prior experience with pharmaceutical regulatory technologies like Documentum, Veeva, Calyx/Ennov RIM, Lorenz

Deep understanding and experience in high quality digital delivery, including planning, dependency management, change control, risk, compliance and governance

Strong verbal and written communication skills with ability to confidently present complex information to all levels of the organization is required

Maintain and advance a positive team culture and support an authentic, open, and broad environment that improves diverse experiences and perspectives

Preferred:

Experience in the use of Agile methodology

Experience with Veeva RIM product suite

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Hyderabad, India
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 594 comparable Regulatory Affairs roles across 117 biopharma companies.

594Comparable roles tracked
539Currently active
117Companies hiring similar roles
54Countries represented

Salary context

166 of 594 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $75,038 – $380,750 (median $198,000)

Where these roles are based

Top locations among the 594 comparable roles

United States244
India45
United Kingdom34
Japan34
Poland27
Ireland21

+ 48 more countries

Seniority mix

460 of 594 peers have a known seniority level

Manager181
Director78
Senior58
Associate Director55
Senior Director25
Intern/Fellow/Postdoc25
Principal16
Associate13
Executive/VP9

Therapeutic area mix

48 of 594 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology18
Immunology10
Rare Disease6
Dermatology & Aesthetics5
Vaccines & Infectious Disease3
Neuroscience3
Cardiovascular / CVRM2
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Regeneron India Private Limited Hyderabad, India Manager
Same function Same country
40%similar
Regeneron India Private Limited Hyderabad, India Manager
Same function Same country
40%similar
Regeneron India Private Limited Hyderabad, India Associate Director
Same function Same country
40%similar
Regeneron India Private Limited Hyderabad, India Manager
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Regulatory Affairs job in India, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Manager CMC Regulatory Affairs
Regeneron India Private Limited · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
40%
Senior Manager Triage
Regeneron India Private Limited · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
40%
Regulatory Affairs Manager (CMC)
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
40%
Regulatory Compliance Change Assessor - Manager
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.