We are eager to add a diligent Regulatory Compliance Manager to join our amazing team at Johnson and Johnson in Irving, TX.
Growing your career as a Full Time Regulatory Compliance Manager is an outstanding opportunity to develop critical skills.
If you are strong in adaptability, analysis and have the right passion for the job, then apply for the position of Regulatory Compliance Manager at Johnson and Johnson today!
Johnson & Johnson Medical Devices a member of the Johnson & Johnson Family of Companies is recruiting for a Regulatory Compliance Manager ! This position will be located in Irving, TX.
Mentor Worldwide, LLC, a member of Johnson & Johnson's Medical Devices Companies, is recruiting for a Regulatory Compliance Manager for our Irving, Texas location!
Mentor is a leading supplier of breast implants in the global aesthetic market. The company develops, manufactures, and markets innovative, science-based products for surgical and non-surgical medical procedures that allow breast surgery patients to improve their quality of life. The company is focused on two strategic areas: breast reconstruction and breast augmentation. MENTOR® is the only manufacturer whose silicone breast implants are made in the U.S.A. For over 20 years, more than 5 million women have chosen MENTOR® Breast Implants. Position Summary:
Under the management of the Regulatory Compliance Director CSS this position will have the objective of maintaining high quality standards for the product manufacturing process and compliance with all applicable regulatory requirements. In addition, this position is responsible for the absence of significant quality issues and regulatory compliance actions by government agencies. Replaces in case of absence: Regulatory Compliance Director CSS ; as duties as assigned. Key Responsibilities:
Under general direction and in accordance with all applicable federal, state and local
laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: 1. External inspection readiness and associated activities. Lead and manage site audit.
readiness activities to always ensure inspection readiness.
• Prepare and host external audits: e.g. Notified Body, Ministry of Health country inspections, FDA, J&J Corporate Audits for site. Responsible for effective regulatory agency inspections.
• Audit preparation activities (auditor logistics, front room/back-room arrangements, identifying/preparing SME's, etc.).
• Assess the risk and applicability of audit observations from other J&J facilities to
determine impact to the site.
• Schedule and manage mock inspections as part of External Inspection Readiness
activities.
• Provide timely information to support the inspection process, including those that maybe taking place at other sites / locations.
• Provide daily inspection communications regarding potential non-conformities.
• Prepare responses to any external inspection or other regulatory notification associated with site.
• Ensure adequate corrective actions for external audit observations related to site, including investigations, monitor and drive on-time completion of CAPA plans, perform follow-up with CAPA owners, and perform effectiveness monitoring and closure. 2. Internal Audit Program and Management Execution: Curriculum and Proficiency Establish and execute an effective internal audit schedule for site.
• Execute against established internal audit procedures.
• Ensure adequate corrective actions for internal audits, including investigations and corrective action plans, drive on-time completion of CAPA plans, perform follow-up with CAPA owners, and perform effectiveness monitoring and closure.
• Drive compliance and improvement in internal audit metrics.
• Ensure quality system is periodically evaluated and audited and appropriate preventive/ corrective action is taken to meet the business and regulatory requirements.
• Where appropriate, execute program(s) for training and evaluating qualifications of auditors. Note: Programs can include franchise, supply chain, sector, and/or enterprise elements. 3. Enterprise/ Sector Support
• Participate in JJRC audits as requested.
• Where appropriate assure representation on all required business unit, sector, and/or enterprise teams (e.g., Do it Right)
• Support the creation and effective deployment of internal J&J Quality System and/or
• Compliance standards.
• Connect and collaborate with CSS Regulatory Compliance team and other regions. 4. CURVE Reporting
• Assure that required compliance-related events (e.g., field actions, inspections) are entered into CURVE per required timeframes.
• Assure that CURVE information is current and updated in a timely manner. 5. Metrics Collection and Reporting
• Assure that Quality & Compliance metrics are consistently and accurately captured, and that metrics are captured at the appropriate level for subsequent analysis and reporting (e.g., site level, supply chain).
• Drive compliance to Quality and Compliance metric targets.
• Create reports and communicate performance against metrics to key stakeholders.
• Highlight/communicate adverse trends in metrics and take risk-based action to remediate. 6. Escalations
• Escalate items in accordance with established procedures.
• Provide routine communication, updates and escalation to site and franchise organizational management regarding compliance trends and initiatives.
• Responsible for the proactive identification and alerting of management of quality issues in time to resolve potential adverse effects to the customer, company image/reputation and/or the business. 7. External Standards and Regulations
• Proactively assess and influence the external environment by participating on industry and regulatory body work teams. As appropriate collect and provide site input.
• Communicate outcomes and trends to key stakeholders.
• Support implementation of new external standards/regulations for Supply Chain Sites.
• Maintain current knowledge of regulatory changes through industry publications. 8. Site Management Review
• Provide input into Site Management Reviews (e.g., internal audits.) to allow meaningful review. Education:
A minimum of a Bachelor's or equivalent University degree is required. Required:
• A minimum of 8 years' experience in Regulatory Compliance, Quality roles and Medical Device Industry, including 2-3 years specific experience in a management/supervisory role.
• Working Knowledge of 21 CFR Part 820, QSR, ISO 13485, SOR 98-282 CMDR (Canada Medical Device Regulations, J-PAL (Japanese), MDD (European) requirements, and knowledge of Brazil GMP and other applicable regulations and standards.
• Experience, supporting and managing Health Authority & Notified Body Inspections, managing internal audit program, expertise in ISO 13485, EUMDR, FDA CFR 820
• Balanced technical understanding of products and processes combined with superior business and compliance acumen.
• Ability to discern critical issues amidst broad operating unit complexity and to engage and achieve executive management support for proactive and reactive measures. Preferred:
• Current certification of quality system auditor or lead auditor (ISO13485 Lead Auditor Certification) Other:
• This position may require up to 10% domestic & international travel.
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
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Benefits of working as a Regulatory Compliance Manager in Irving, TX:
? Career Growth Potential
? Opportunities to grow
? Competitive salary
