Local Compliance Manager

Antwerp - Belgium

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

The job posting is outdated and position may be filled

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:

R&D Operations

Job Sub Function:

Clinical Trial Project Management

Job Category:

Professional

All Job Posting Locations:

Beerse Antwerp Belgium Breda Netherlands

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at are looking for a driven Local Compliance Manager to join our Clinical Operations team in The Netherlands and Belgium. You will contribute in building a strategically sound local quality plan to ensure our clinical trials will be delivered to the highest quality standards and are following all applicable SOPs laws and regulations. You will also ensure our team is adequately trained and onboarded. Our new colleague should be flexible and able to work independently. We are seeking to hire a strong communicator a leader and team player with quick learning and problem-solving abilities. The Compliance Manager will collaborate with the Country Head the Clinical Research Managers and the teams carrying out the clinical trials consisting of Local Trial Managers (LTM) Site Managers (SM) and Clinical Trial Assistants (CTA). You will be part of a hardworking enthusiastic and committed team of /- 170 people eager to deliver and helping to improve the lives of millions of patients.

Principal Responsibilities:

Quality and Compliance Oversight: Contribute in building a local longterm strategically sound quality plan; proactively measure and identify compliance risks and define remediation actions; supervise progress and confirm effectiveness of remediation plans and conduct QC checks on trials and processes; lead preparation and oversight of inspections and audits and the management of CAPAs; leads process improvement initiatives.
Local onboarding and consultation: support onboarding of new hires; organize local workshops trainings and lessons learned to increase compliance awareness. Be the go-to person for risk management and provide advice for complex situations to ensure timely resolution of issues.
Local regulatory intelligence: perform impact assessments of new/revised local regulations and provide clear and timely guidance to the teams. Keep local intelligence up to date.
Collaboration with business quality: perform local supplier assessments; coordinate annual due diligence update certification and training of local suppliers.
Leads local compliance meetings.
Leads and/or participates in special (global) initiatives as assigned.
May assume additional responsibilities or special initiatives such as Champion Subject Matter Expert or Business Process Owner.

Education and Experience Requirements:

BA/BS degree in Life Sciences or related scientific field (or 8-10 years equivalent experience)
A minimum of 6 years of previous pharmaceutical industry experience is required with at least 4-6 years of GxP experience within clinical research and/or quality assurance. Other relevant working experiences and skills may be considered by the hiring manager. Experience in phase 1 2 3 clinical trials is a plus.
Strong proven understanding of GCP local laws and regulations
Advanced skills and knowledge of business processes and practices
Ability to present in a clear and concise way - strong communication skills
Strong interpersonal skills
Proven project leadership skills
Willingness to engage with authorities trade associations and key sites
Proficient in Dutch English and French (for Belgian candidates)

Required Skills:

Preferred Skills:

Analytical Reasoning Budgeting Clinical Trial Management Systems (CTMS) Clinical Trials Compliance Management Contract Management Execution Focus Fact-Based Decision Making Laboratory Operations Mentorship Process Improvements Project Integration Management Research and Development Research Ethics Standard Operating Procedure (SOP) Technical Credibility

Required Experience:

Manager

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Project Management

Job Category:

Professional

All Job Posting Locations:

Beerse Antwerp Belgium Breda Netherlands

Job Description:

About Innovative Medicine

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Principal Responsibilities:

Quality and Compliance Oversight: Contribute in building a local longterm strategically sound quality plan; proactively measure and identify compliance risks and define remediation actions; supervise progress and confirm effectiveness of remediation plans and conduct QC checks on trials and processes; lead preparation and oversight of inspections and audits and the management of CAPAs; leads process improvement initiatives.
Local onboarding and consultation: support onboarding of new hires; organize local workshops trainings and lessons learned to increase compliance awareness. Be the go-to person for risk management and provide advice for complex situations to ensure timely resolution of issues.
Local regulatory intelligence: perform impact assessments of new/revised local regulations and provide clear and timely guidance to the teams. Keep local intelligence up to date.
Collaboration with business quality: perform local supplier assessments; coordinate annual due diligence update certification and training of local suppliers.
Leads local compliance meetings.
Leads and/or participates in special (global) initiatives as assigned.
May assume additional responsibilities or special initiatives such as Champion Subject Matter Expert or Business Process Owner.

Education and Experience Requirements:

BA/BS degree in Life Sciences or related scientific field (or 8-10 years equivalent experience)
A minimum of 6 years of previous pharmaceutical industry experience is required with at least 4-6 years of GxP experience within clinical research and/or quality assurance. Other relevant working experiences and skills may be considered by the hiring manager. Experience in phase 1 2 3 clinical trials is a plus.
Strong proven understanding of GCP local laws and regulations
Advanced skills and knowledge of business processes and practices
Ability to present in a clear and concise way - strong communication skills
Strong interpersonal skills
Proven project leadership skills
Willingness to engage with authorities trade associations and key sites
Proficient in Dutch English and French (for Belgian candidates)

Required Skills:

Preferred Skills:

Required Experience:

Manager

Key Skills

Apply Now

About Company

Johnson & Johnson

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

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