Logo for Zoetis

Director Regulatory Affairs and Affiliate Quality, Central and Eastern Europe

Role overview

Qualifications

  • University degree in veterinary medicine, pharmacy, or biological/chemical science
  • Regulatory, Quality and/or Pharmacovigilance experience in veterinary or human health (pharmaceuticals and/or vaccines)
  • Experience in leading people
  • Knowledge of the European animal health market and business environment

Responsibilities

  • Lead the CEE Regulatory Affairs Affiliate Quality Team, ensuring Maintenance of Marketing Authorisations and compliance with GMP/GDP
  • Act as an active member of the Europe Middle East Regulatory Leadership Team
  • Oversee the Geographic Expansion Procedure in CEE, balancing stakeholder needs and ensuring compliance
  • Manage Affiliate Quality Operations for Distributor Markets in the CEE region, and support CEEME Commercial Leadership Team

About the company

Zoetis logo

Zoetis

Pharmaceutical Manufacturing

The world’s leading animal health company. Zoetis is driven by a singular purpose: to nurture our world and humankind by advancing care for animals. We’ve been innovating ways to predict, prevent, detect, and treat animal illness for over 70 years, and we continue to stand by those raising and caring for animals worldwide – from veterinarians and pet owners to livestock farmers. Our leading portfolio and pipeline of medicines, vaccines, diagnostics and technologies make a difference in over 100 countries. Community Guidelines: This page is intended for learning more about how Zoetis is advancing care for animals. We aspire to create a supportive community, but there are some guidelines to which posts and comments on this page must adhere. If your post references a side effect related to any Zoetis product, we may contact you for more information. To monitor the safety of Zoetis products, we advise you to call our Veterinary Medical Information and Product Support Team at 1-888-963-8471; Support Team is available Mon-Fri 9am to 6:30pm ET. We reserve the right to remove any post/comment that violates LinkedIn Guidelines. We respectfully request that you refrain from posting comments including: Unsolicited and/or unverified medical advice Vulgarity and/or profanity Discriminatory and/or derogatory comments, hate speech Politics and religion Personal attacks and/or threats Promotion of illegal activity Copyright/trademark infringements Topics that may be considered spam/advertising Our regular business hours are Mon-Fri 9am to 5pm ET. Zoetis does not endorse and is not responsible for information and opinions shared by community members. The information shared is provided for educational purposes only and is not intended to replace discussions with an animal healthcare professional. Testimonials represent individual experience only and the experiences and opinions of community members may be unique to the speaker. Terms of Use: https://www.zoetis.com/terms-of-use

Company details

Company typeXLarge
IndustryPharmaceutical Manufacturing
Company size10001

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

Job description

Locations under consideration include Zaventem (hybrid) , Warsaw and EU Remote.

Role Description

We are looking for a Director to lead the Regulatory Affairs and Affiliate Quality team in Central & East Europe (CEE: Poland, Czechia, Slovakia, Hungary, Baltics, Balkans and Ukraine).  This role entails leading a team of 16 colleagues (7 of whom are direct reports) to ensure that the Regulatory Affairs and Affiliate Quality needs of the Commercial Operations are met.

The position reports to the Senior Director Regulatory Affairs and Affiliate Quality, Europe and Middle East (EME).  It will be based in Zaventem, Belgium, or Warsaw, Poland and will involve 10 - 20% European travel.

Responsibilities

  • To lead the CEE Regulatory Affairs & Affiliate Quality Team, ensuring that Marketing Authorisations (product licences) are maintained, all products supplied to customers meet the relevant GMP/GDP and Zoetis internal requirements, and pharmacovigilance reporting obligations are met
  • To be an active member of the Europe & Middle East Regulatory Leadership Team and an associate member of the Central & East Europe and Middle East (CEEME) Commercial Leadership Team
  • To oversee the Geographic Expansion Procedure in CEE, balancing the needs of all stakeholders (Commercial, R&D and Global Manufacturing & Supply) and ensuring compliance with the agreed procedures and timelines
  • To influence and ensure alignment of CEE Regulatory Affairs, Affiliate Quality and pharmacovigilance strategies and procedures with:
    • corporate strategies, procedures and systems
    • regulatory requirements of EU and National Authorities
  • To actively manage Affiliate Quality Operations for Distributor Markets in the CEE region, including maintenance and execution of the Quality Management System (QMS)
  • To support the CEEME Commercial Leadership Team in all matters concerning Regulatory Affairs, Affiliate Quality, and Pharmacovigilance, including but not limited to:
    • Ensuring participation in regional and global projects, as required
    • Representing Zoetis at Industry Associations
    • Maintaining an awareness of changing legislation and guidance, and review of Public Affairs materials from a regulatory perspective
  • Participate in team activities and travel, as appropriate
  • Other specific duties and responsibilities as detailed in annual Objectives, or agreed with Line Manager

Requirements

  • University degree in veterinary medicine, pharmacy, or biological/chemical science
  • Regulatory, Quality and/or Pharmacovigilance experience in veterinary or human health (pharmaceuticals and/or vaccines)
  • Experience in leading people
  • Knowledge of the European animal health market and business environment would be an advantage
  • Excellent communication skills in English

 

 

Full time

 

 

Regular

 

 

Colleague

 

 

Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.

Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.

 

 

Notice: Zoetis Recruiters will contact candidates via email from an address ending in @zoetis.com and may also initially connect with candidates through LinkedIn, including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that does not come from @zoetis.com, please treat it as suspicious. For your security, do not reply, click links, open attachments, share personal or financial information, or send money in response to unexpected or questionable recruitment communications.

 

 

 

 

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Regulatory Affairs Manager Related jobs

Other jobs at Zoetis

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.