Regulatory Affairs Partner

Roche

Fatih

On-site

TRY 180,000 - 320,000

Full time

6 hours ago
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Job summary

Roche in Turkey seeks a Regulatory Affairs professional to lead strategies for new products and indications, enabling fast market access and compliant launches. You will coordinate submission timelines, adapt global dossiers to local requirements, and ensure GMP and audits readiness, working closely with cross-functional teams and health authorities.

Turkish and English fluency is required, with a collaborative mindset.

Qualifications

  • Solid knowledge of regulatory processes and requirements.
  • Experience in cross-functional project settings.
  • Willingness to share knowledge within the team.
  • Strong communication and team orientation.

Responsibilities

  • Develop regulatory strategies for Roche's new products and indications.
  • Define submission timelines and plan launch dates.
  • Manage GMP, prioritization, and registration submissions.
  • Adapt global dossiers to local regulatory requirements.
  • Design policy initiatives to shape Turkish regulations.
  • Ensure GMP/regulatory audit readiness.
  • Collaborate with cross-functional teams for launch planning.
  • Engage with health authorities and industry groups.
  • Handle correspondence for registered and unregistered products with the Ministry.

Skills

Regulatory strategy
GMP knowledge
Cross-functional teamwork
Turkish language
English language
Project coordination
Compliance awareness

Education

Bachelor's degree in Pharmacy, Chemical Engineering, Chemistry

Job description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position
Key Responsibilities
  • Develop innovative regulatory strategies for Roche's new products and indications to enable fast market access
  • Define regulatory submission and approval timelines, and plan launch dates accordingly
  • Manage GMP, prioritization, and registration submissions for innovative products
  • Adapt global product dossiers to meet local regulatory requirements; gather and prepare additional documentation as needed
  • Design and implement policy initiatives to shape the Turkish regulatory environment in alignment with Roche's strategy
  • Ensure inspection-readiness for GMP and regulatory audits; manage related processes within relevant systems
  • Collaborate closely with cross-functional teams for the launch planning of new products or indications
  • Engage in effective advocacy activities with health authorities, industry associations, and key stakeholders
  • Conduct the necessary correspondence for all registered/non-registered products and follow up with the Ministry processes
Who You Are
  • Bachelor's degree in Pharmacy, Chemical Engineering, Chemistry, or a related field
  • Minimum 3 years of experience in regulatory affairs, ideally working in cross-functional settings
  • Hands-on knowledge and solid understanding of regulatory processes and requirements
  • Preferably, some experience in coordinating or supporting project activities within a team environment
  • A collaborative mindset with the ability to motivate colleagues and contribute to team development
  • Willingness and capability to share knowledge, provide support, and offer guidance within the team when needed
  • Strong communication skills and a team-oriented approach
  • High ethical standards and a basic understanding of relevant compliance regulations
  • Proficiency in both written and spoken Turkish and English
  • Comfortable working in a dynamic, agile environment; open to change, self-motivated, responsible, and eager to learn
Who we are

A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let's build a healthier future, together.

Roche is an Equal Opportunity Employer.

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