Regulatory Affairs Manager
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 jnj.com .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Istanbul, Turkey
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Regulatory Affairs Manager to be based in Istanbul / Türkiye.
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Position Summary:
To lead regulatory activities across a diverse pharmaceutical portfolio within the TURGAN Cluster. Reporting directly to the Head of Regulatory Affairs, TURGAN Cluster, this role is responsible for developing and executing regulatory strategies, managing product registrations and lifecycle activities, ensuring compliance with local regulations, and serving as a key partner within cross-functional value teams.
A responsible person will lead regulatory submissions, labeling updates, health authority interactions, and regulatory intelligence activities while contributing to portfolio growth, business objectives, and patient access. The role requires strong collaboration with local, regional, and global stakeholders, proactive management of regulatory risks and opportunities, and effective representation of the company with health authorities and industry associations.
Key Responsibilities
Regulatory Strategy & Portfolio Management
Develop and execute regulatory strategies for new products, new indications, renewals, and other lifecycle management activities.
Provide strategic regulatory input to support portfolio and business objectives.
Assess regulatory risks, opportunities, and health authority expectations.
Monitor and communicate regulatory developments that may impact the business.
Submissions & Lifecycle Management
Lead preparation, review, submission, and approval tracking of regulatory dossiers.
Manage marketing authorization applications, variations, renewals, and labeling updates.
Ensure timely implementation of approved changes within company systems and processes.
Support activities required for new product launch
Stakeholder Engagement
Build and maintain strong relationships with health authorities, industry associations, internal & external partners, and key stakeholders.
Represent the company in external regulatory forums and industry working groups when appropriate.
Compliance & Quality
Ensure compliance with all applicable regulations, company policies, and ethical standards.
Support inspections, audits, and regulatory assessments.
Maintain accurate regulatory documentation and archival systems.
Cross-Functional Leadership
Partner with Medical Affairs, Supply Chain, Quality, Legal, Market Access, Government Affairs, Commercial, and Global Regulatory teams to deliver business objectives.
Contribute as a key Regulatory representative within Cross-Functional Value Teams (CVTs).
Support knowledge sharing, continuous improvement, and operational excellence initiatives.
Qualifications & Requirements:
Ideal Candidate Profile
Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, Life Sciences, or related discipline.
Available to work with the Hybrid working model (3 days office, 2 days home)
Minimum 8 years of Regulatory Affairs experience within the pharmaceutical industry.
Minimum 2-3 years of Regulatory Affairs Manager experience, demonstrated success in working cross-functional teams and complex regulatory projects.
Strong knowledge of Turkish pharmaceutical regulations and regulatory procedures.
Demonstrated experience in regulatory strategy, submissions, and lifecycle management.
Effective stakeholder management skills.
Strong communication, influencing, and leadership capabilities.
Fluent English & Turkish
Results-oriented, strategic thinker with strong planning and organizational skills.
Following and matching with our Credo values
Required Skills:
Preferred Skills:
Analytical Reasoning, Business Writing, Coaching, Compliance Risk, Fact-Based Decision Making, Industry Analysis, Legal Support, Process Improvements, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Strategic Thinking, Technical Credibility
Job details
How this role compares
Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.
We currently track 192 comparable Manager Regulatory Affairs roles across 64 biopharma companies.
Salary context
52 of 192 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 192 comparable roles
+ 27 more countries
Seniority mix
192 of 192 peers have a known seniority level
Therapeutic area mix
16 of 192 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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.
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.
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.
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.