Senior Compliance Lead

Johnson & Johnson Innovative Medicine; Geel; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

Johnson & Johnson Innovative Medicine is seeking a senior Quality & Compliance Lead for the Geel site to own the internal audit program and external GMP inspections. You will deploy compliance initiatives, train auditors, and coordinate cross-site compliance teams.

You will lead CAPA-driven remediation, ensure inspection readiness, and partner with Regulatory, Operations, and Product Quality teams to mitigate risk and uphold J&J standards worldwide.

Qualifications

• Fluent in Dutch and English (written and spoken).
• At least 8 years related experience in GMP-regulated industry with 3+ years in regulatory compliance.
• Experience performing internal or external audits is required.

Responsabilités

• Accountable for Geel site internal audit program and external GMP inspection management.
• Act as compliance SME and deploy compliance initiatives at Geel aligning with Regulatory Compliance strategy.
• Coordinate Geel-based compliance personnel and support Beerse, Geel, Athens and Cork teams.
• Lead site internal audits, inspection readiness, CAPA assignment and site response efforts.
• Partner with Quality to manage inspections and provide input to daily inspection summaries.
• Establish department policy, SOPs, and working practices; drive compliance improvement across the site.

Connaissances

Dutch

English

Agile Internal Audit

Analytical Reasoning

Audit and Compliance Trends

Regulatory Compliance

Quality Auditing

Risk Management

Third-Party Auditing

Formation

Bachelor’s Degree in Science or related field

Description du poste

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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:

Quality

Job Sub Function:

Quality & Compliance Audit

Job Category:

Professional

All Job Posting Locations:

Geel, Antwerp, Belgium

Job Description:

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 https://www.jnj.com.

Objectives and Responsibilities

Accountable for the Geel site internal audit program and external GMP inspection management (e.g. Health Authority, Customer).

Acting as compliance Subject Matter Expert and deploy compliance initiatives at the Geel site in alignment with the Pharmaceutical Regulatory Compliance strategy.

Coordinate team of Geel-based compliance personnel

Support the compliance teams of Beerse, Geel, Athens and Cork SM to deliver the site internal audit program and external GMP inspection management program.

Responsibilities IMRC Compliance Lead for Geel

• Responsible for site internal audit program including:
• Establish and create schedule
• Auditor training (qualify and evaluate)
• Execute internal audits (schedule, issue agenda, prepare, conduct audit, issue report)
• Execute compliance walk-throughs (e.g. IWR)
• Evaluate responses to internal audits
• Enter internal audit data in Comet
• Maintain site inspection readiness program for external GMP audits and inspections (Health Authority, Customer). Including:
• Facilitate inspection management (front room, back room, coaching)
• Lead the site response efforts including assignment of appropriate CAPAs
• Inspection Readiness (audit preparation, schedule and manage mock inspections, SME coaching)
• Partner with Quality to manage inspections (host and/or coordinate front room and back room, daily inspection summaries)
• Review site response and associated CAPA for Health Authority inspections
• Provide input to daily inspection summaries, as needed
• Identify changes in regulations that impact compliance procedure, perform gap analysis against current practices. Implement J&J Compliance Stds (e.g. Audit/Inspection Mgt) and partner with sites on J&J standard implementation
• Provide Compliance Subject Matter Expertise (SME) for site personnel, Quality Systems and/or projects. As needed, review complaints and field actions.
• Ensure appropriate and timely escalation of risks to the appropriate leadership and regulatory compliance teams. Facilitate remediation of compliance risks
• Represent Regulatory Compliance at Site Management Reviews, CAPA Review Boards, Escalations, Platform Compliance mtgs, etc.
• Partner with site for execution of proactive compliance scans.
• Partner with site and segment personnel (e.g. Regulatory Affairs, Operations, Product Quality Mgt, etc.) to proactively identify risks and drive compliance improvement across the site.
• Establish a high performance and continuous improvement culture driven by key performance metrics, benchmarking and sharing of best practices
• As applicable, report progress of site compliance remediation plans (e.g. MCAP, SDCAP, etc.)
• Collaborate with other groups in IMRC and JJRC to support execution of independent audits and special assessments. Support site during ERC audits (e.g. document review, front/back room support). Review and provide input to site response, and associated CAPA, to ERC audits.
• Coordinate, maintain, report and drive site compliance metrics.
• Establish department policy, standard operations procedures and working practices.
• Coordinate compliance training for the site
• Support Quality and Compliance strategy implementation
• Connect with external groups (e.g. PDA, ISPE, etc.) to benchmark industry standards
• As needed, provide training for Quality concepts and/or systems.
• As needed, co-authors, review and revise compliance procedures.
• As needed, review (not approve) significant manufacturing and laboratory investigations, confirmed complaints and S1/S2 Field Actions.
• Partner with the site for execution of the site assessment as part of the SHARE program
• Connect with site personnel in context of the compliance awareness (CARE) program

Environment, Health & Safety (EHS)

• Always uses the appropriate prevention rules and procedures
• Uses the available personal and collective protection materials correctly
• Works neat and tidy
• Reports (near) accidents, incidents, deviations and risky situations
• Cooperates on and suggests solutions to improve safety, health an environment
• Participate actively on promotion campaigns, working on the safe behaviour program, prevention controls
• Addresses to other colleagues and third persons when prevention procedures are not followed or in case of unsafe behaviour

Credo

• Takes into account the credo values in all daily activities
• Integrates the Credo dialogue in the IMRC department

Profile needed for this function

Knowledge

• At least 8 years related experience in a GMP-regulated industry and at least 3 years of regulatory compliance experience.
• Extensive knowledge of global GMP regulations is required
• Experience performing internal or external audits is required.
• Ability to build partnerships and mediate issues while optimizing the value proposition.
• Strong analytical skills and ability to clearly articulate issues.
• Excellent communication skills, able to quickly build credibility within the Quality and Compliance community, and executive management.
• Delivers on commitment timelines and has high sense of urgency.
• Demonstrate business acumen, deal with complexity and ambiguity

Degree

Bachelor’s Degree in Science or related field

Languages

Fluent in Dutch and English (written and spoken)

Quality: #SCQuality

Required Skills:

Preferred Skills:

Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Compliance Frameworks, Compliance Management, Compliance Policies, Compliance Risk, Critical Thinking, Organizing, Quality Auditing, Quality Control (QC), Quality Standards, Regulatory Compliance, Risk Management, Technical Credibility, Third-Party Auditing