Project manager, CEE, Balkan and Baltics

Posted 7 Days Ago
Be an Early Applicant
3 Locations
In-Office
1M-2M Annually
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Lead and coordinate cross‑country QARA quality and regulatory projects across CEE, Balkan and Baltics. Develop project plans, track milestones and risks, engage cross‑functional stakeholders, ensure compliance with quality systems and regulatory requirements, deliver reporting to senior leadership, and drive process improvements to support patient safety and operational excellence.
Summary Generated by Built In

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:

Maroussi - Athens, Attiki, Greece, Prague, Czechia, Warsaw, Masovian, Poland

Job Description:

DePuy Synthes is recruiting for a Project manager, CEE, Balkan and Baltics, located in Prague, Czech Republic.

Job Overview 

The Project Manager, CEE, Balkan & Baltics plays a critical role within QARA International, leading and coordinating crosscountry quality and regulatory projects across Central & Eastern Europe, Balkan & Baltics markets. This role ensures that regional initiatives are delivered on time, within scope, and in alignment with DePuy Synthes quality systems and regulatory commitments. The position offers strong visibility across international stakeholders and provides the opportunity to directly impact patient safety, compliance, and operational excellence in a complex, multicountry environment. 

  

Key Responsibilities 

  • Lead and manage QARArelated projects across CEE, Balkan & Baltics countries, ensuring alignment with global and regional strategies. 

  • Develop and maintain project plans, timelines, milestones, and risk registers, tracking progress and ensuring timely delivery. 

  • Coordinate crossfunctional and crossregional stakeholders, including Quality, Regulatory Affairs, Supply Chain, and Commercial teams. 

  • Monitor project risks, issues, and dependencies, driving mitigation plans and escalation where required. 

  • Support implementation of quality system initiatives, regulatory changes, and process improvements across the region. 

  • Prepare and deliver clear project reporting and communications to senior QARA and business leadership. 

  • Ensure project activities comply with internal quality standards, regulatory requirements, and governance expectations. 

  • Promote a culture of continuous improvement, collaboration, and accountability within project teams. 

  

Qualifications 

Education 

  • Bachelor’s degree required in Engineering, Life Sciences, Quality, Regulatory Affairs, Business, or a related discipline. 

  • Advanced degree (e.g., Master’s) preferred. 

Experience and Skills 

Required: 

  • Demonstrated experience in project management within a regulated or matrixed environment. 

  • Experience coordinating crossfunctional and international stakeholders. 

  • Solid understanding of quality systems, compliance, or regulatorydriven processes. 

  • Ability to communicate clearly with diverse audiences, including senior leadership. 

  • Proven ability to manage multiple priorities and deliver results in a dynamic environment. 

Preferred: 

  • Experience supporting QARA, Commercial Quality, Quality, or Regulatory Affairs projects within medical devices, pharmaceuticals, or healthcare. 

  • Familiarity with CEE and Balkan regulatory or business environments, particularly NonEU markets. 

  • Experience with process improvement or change management initiatives. 

  • Knowledge of project management methodologies (e.g., PMP, Agile, or similar frameworks). 

  • Strong planning, organizational, and riskmanagement skills. 

Other: 

  • Language: Fluency in English required; additional regional languages are an advantage. 

  • Travel: Limited international travel required, primarily within CEE & Balkan regions. 

  • Certifications: Project Management certification (e.g., PMP, PRINCE2) preferred but not required. 

  

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com. 

 

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes. 

 

 Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. 

  

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. 

  

#LI-Hybrid 

#DePuySynthesCareers



Required Skills:



Preferred Skills:

Analytical Reasoning, Business Writing, Coaching, Collaboration, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking

  


The anticipated base pay range for this position is:

Kč1,043,000.00 - Kč1,679,000.00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.


*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.



Skills Required

  • Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, Business, or related discipline
  • Demonstrated experience in project management within a regulated or matrixed environment
  • Experience coordinating cross‑functional and international stakeholders
  • Solid understanding of quality systems, compliance, or regulatory‑driven processes
  • Ability to communicate clearly with diverse audiences, including senior leadership
  • Proven ability to manage multiple priorities and deliver results in a dynamic environment
  • Fluency in English
  • Advanced degree (e.g., Master's)
  • Experience supporting QARA, Commercial Quality, Quality, or Regulatory Affairs projects in medical devices, pharmaceuticals, or healthcare
  • Familiarity with CEE and Balkan regulatory or business environments, particularly Non‑EU markets
  • Experience with process improvement or change management initiatives
  • Knowledge of project management methodologies (e.g., PMP, Agile) or project management certification
  • Additional regional languages
  • Strong planning, organizational, and risk‑management skills

Johnson & Johnson Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Johnson & Johnson and has not been reviewed or approved by Johnson & Johnson.

  • Healthcare Strength Healthcare coverage is characterized as comprehensive across medical, dental, and vision, with added supports like onsite clinics, fitness centers, and Employee Assistance resources. Mental-health services and wellbeing reimbursements are also described as meaningful components of the overall package.
  • Retirement Support Retirement offerings are portrayed as a major differentiator, combining a 401(k) with employer matching and an employer-funded pension plan. Stock options and other long-term financial supports are also positioned as part of the broader rewards mix.
  • Parental & Family Support Family-related benefits are presented as notably strong, including paid parental leave for all new parents and additional leave types for caregiving and bereavement. Financial assistance for adoption, fertility treatment, and surrogacy is highlighted as a significant support.

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The Company
HQ: New Brunswick, NJ
143,612 Employees
Year Founded: 1886

What We Do

Profound Change Requires Boldness. Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world. Social Media Community Guidelines: http://www.jnj.com/social-media-community-guidelines

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