Regulatory Affairs Associate

Job Description :

Regulatory Affairs Associate

At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world.

Joining our Regulatory team, you will be part of an empowering and collaborative culture where your work plays a key role in ensuring patient safety, regulatory compliance and sustainable access to medicines. By working closely with cross-functional teams and external stakeholders, you will support regulatory excellence, life-cycle management and the consistent maintenance of our portfolio. Your contribution helps ensure that high-quality therapies remain available, compliant and trusted throughout their entire life cycle.

Ferring+You

We are looking for a Regulatory Affairs Associate to join our team and take a key role in regulatory compliance, quality assurance, document governance, and cross-functional business support in line with local regulations and global procedures, reporting directly to the Regulatory Affairs Manager.

Your day at Ferring

Act as Document Accountable Person (DAP) and Document Controller (DC), ensuring document lifecycle management, consistency, and compliance

Serve as the main local regulatory contact and manage regulatory compliance activities

Coordinate new drug approvals, including dossier preparation, submissions, and follow-up with local Health Authorities

Manage regulatory submissions, variations, renewals, and product lifecycle activities

Support and coordinate regulatory inspections and maintain validity of licenses and certificates

Monitor regulatory intelligence, assess impact, and proactively communicate regulatory changes

Ensure timely and accurate updates in global and local regulatory systems (e-CTD, Veeva Vault, Track Wise, etc.)

Prepare, review, and approve artworks and labeling to support submissions and product launches

Review promotional and non-promotional materials in line with local regulations and global procedures

Support Quality Management System (QMS) implementation and sustainability, including local market release

Support regulatory and pricing applications, including document coordination and pricing data monitoring

Behind our collaboration…There’s you

University degree in Pharmacy

Min. 2-3 years of practical experience in regulatory and quality assurance

Know-how of interactions with regulatory authorities

Experience with e-CTD, Veeva Vault, Track Wise, and pricing is a plus

Eager to learn personality, team player approach, attention to details

Fluent in English language (written and verbal)

People come first at Ferring

Get inspired from our commitment to advocate for everyone’s right to build a family, no matter who you are, where you live or who you love

Our inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role

Parental leave for both birthing and non-birthing parents

Extended support on family building journey

Making a difference in the life of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member’s contributions. Imagine the power of your career when it’s Ferring + You.

Behind our purpose… There’s you

If our mission and your vision are aligned, please apply.

We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status.

Location : Ferring Turkey