Project Manager, Nordics
Copenhagen - Denmark
Job Summary
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .
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 GroupJob Sub Function:
Regulatory AffairsJob Category:
ProfessionalAll Job Posting Locations:
Hellerup Capital DenmarkJob Description:
Location:Ostbanegade 123 Copenhagen Denmark
DePuy Synthes is recruiting for a(n) Project Manager NordicslocatedinOstbanegade 123 Copenhagen Denmark
Johnson & Johnson announced plans to separate our Orthopedics business toestablisha standalone orthopedics companyoperatingas DePuy Synthes.The process of the planned separation isanticipatedto be completed within 18 to24 months subject to legal requirements including consultation with works councils and other employee representative bodies as may be regulatory approvals and other customary conditions and approvals. Should you accept this position it isanticipatedthat following conclusion of the transaction you would be an employee of DePuySynthesand your employment would be governed by DePuy Synthes employment processes programs policies and benefit that case details of any planned changes would be provided to you by DePuy Synthes atan appropriate timeand subject to any necessary consultation processes.
Job Overview
The Project Manager Nordicssupports the planning coordination and delivery ofQARArelatedprojects across the Nordic markets.This role plays a keypartin enabling complianttimelymarket access and business continuity by coordinating crossfunctional initiatives related to regulatory compliance quality system execution and operational readiness.
This position offers broad exposure to regional and global stakeholders and the opportunity to make a tangible impactina highly regulated MedTech environment by supporting quality and regulatory excellence across the Nordics.
Key Responsibilities
Plan coordinate and manage QARArelated projects supporting regulatory compliance quality system activities and market readiness across Nordic countries.
Develop andmaintainproject plans timelines milestones dependencies and risk registers aligned with QARA and businessobjectives.
Coordinate crossfunctional teams including Quality Assurance Regulatory Affairs Supply Chain Operations and Commercial partners.
Track project progressidentifyrisks or issues and drivetimelymitigation and resolution in collaboration with stakeholders.
Support implementation of local market initiatives related to regulatory submissions lifecycle management audits and quality system activities.
Ensure project activitiescomply withinternal policies quality management system requirements and applicable regulatory standards.
Prepare and deliver project status updates dashboards and communications for QARA leadership and key stakeholders.
Contribute tocontinuous improvement initiatives to enhance project execution QARA processes and local market support effectiveness.
Ensuring proactive engagement and shaping of regional policy initiatives that are critical to business strategy continuity and growth.
Qualifications
Education
Required:Bachelors degree in Business Life Sciences Engineering Regulatory Affairs ora relatedfield.
Preferred: Advanced degree or project management certification (e.g. PMP PRINCE2) or training in quality/regulatory disciplines.
Experience and Skills
Required:
46 years of progressive experience in project management quality regulatory support operations or a related role within a regulated industry.
Experience managing crossfunctional projects with multiple stakeholders in a matrixed environment.
Strong organizational planning and documentation skills with high attention to detail.
Ability to manage multiple priorities and deadlines in a dynamic environment.
Strong written and verbal communication skills including stakeholder reporting.
Proficiency with standard project management and office tools.
Preferred:
Experience supporting Quality Assurance and/or Regulatory Affairs activities.
Familiarity with medical devices healthcare or other highly regulated industries.
Exposure tointernationalor multicountry market models.
Experience working in a multinational or matrixed organization.
Project management certification (e.g. PMP PRINCE2 Agile).
Other
Language: English required; Nordic language(s) preferred.
Travel: Limited to moderate regional travel within the Nordics.
Certifications: Project management certifications 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.
#DePuySynthesCareers
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Required Skills:
Preferred Skills:
Analytical Reasoning Business Writing Coaching Collaborating Communication Legal Support Problem Solving Product Licensing Public Policies Regulatory Affairs Management Regulatory Compliance Regulatory Development Regulatory Environment Regulatory Reporting Risk Assessments Strategic ThinkingThe anticipated base pay range for this position is:
kr- krBenefits:
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 locations 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.
Required Experience:
IC
About Company
About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more