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Sr. Compliance Lead

Job in Town of Belgium, Belgium, Ozaukee County, Wisconsin, 53004, USA
Listing for: Get 360Pharma
Full Time position
Listed on 2026-01-02
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Location: Town of Belgium

Engineering, Environmental, Health & Safety

Quality, Compliance, Validation

Regulatory Affairs, Regulatory compliance

Staff, Legal, Public Affairs, Administrative

IT, Enterprise Applications & Systems

About the vacancy

Engineering, Environmental, Health & Safety, Quality, Compliance, Validation, Regulatory Affairs, Regulatory compliance, Staff, Legal, Public Affairs, Administrative, IT, Enterprise Applications & Systems, Expert Bachelor’s Degree (HBO, WO) Permanent Full time 2440 Geel, Belgium

About Your Next Job

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.

About Your Tasks and Responsibilities

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…
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