Director, Quality Systems & Compliance (Devices & Combination Products)
Job title: Director, Quality Systems & Compliance (Devices & Combination Products) in Rahway, NJ at MSD
Company: MSD
Job description: Job DescriptionDirector, Devices & Combination Products Complaints QAWe are seeking a highly motivated and experienced Director of Combination Products Complaints QA to join our team. This role is responsible for leading and supporting the complaints management processes for combination products with a focus on auto-injectors, pre-filled syringes and other innovative drug delivery systems. The ideal candidate will have a strong background and deep expertise in complaint management systems, regulatory reporting and post-market surveillance for combination products.The ideal candidate should also have a proven track record of establishing and managing compliant, scalable complaint processes across pharma, biotech or medical device sectors, and will play a key leadership role in ensuring regulatory compliance, patient safety, and continuous improvement of device complaint quality systems.Key Responsibilities:
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.Employee Status: RegularRelocation: No relocationVISA Sponsorship: NoTravel Requirements: 10%Flexible Work Arrangements: HybridShift: Not IndicatedValid Driving License: NoHazardous Material(s): N/AJob Posting End Date: 05/16/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Expected salary:
Location: Rahway, NJ
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Company: MSD
Job description: Job DescriptionDirector, Devices & Combination Products Complaints QAWe are seeking a highly motivated and experienced Director of Combination Products Complaints QA to join our team. This role is responsible for leading and supporting the complaints management processes for combination products with a focus on auto-injectors, pre-filled syringes and other innovative drug delivery systems. The ideal candidate will have a strong background and deep expertise in complaint management systems, regulatory reporting and post-market surveillance for combination products.The ideal candidate should also have a proven track record of establishing and managing compliant, scalable complaint processes across pharma, biotech or medical device sectors, and will play a key leadership role in ensuring regulatory compliance, patient safety, and continuous improvement of device complaint quality systems.Key Responsibilities:
- Establish and maintain robust complaint handling processes specific to combination products such as auto-injectors and pre-filled syringes
- Develop and refine complaint categories tailored to device related issues to support effective trending and risk management
- Lead and support complaint investigations coordinating with cross-functional teams (e.g. Manufacturing, Technical Operations, Device Development, Safety and Regulatory) ensuring timely completion and CAPA implementation
- Ensure compliance with post-market safety reporting criteria for combination products
- Maintain and improve quality systems in alignment with combination product requirements under 21 CFR Part 4, QMSR, ISO 13485, EU MDR and other OUS regulations
- Represent the company in audits and inspections as the subject matter expert for combination product complaints
- Provide quality oversight of complaint data trending and escalation processes, including preparation of management review metrics, quarterly summaries and regulatory reporting decisions with links into risk assessments and CAPAs as needed
- Collaborate with Pharmacovigilance and Regulatory Affairs on reportable events and periodic safety updates
- Provide expert interpretation of regulations and quality standards related to complaint handling for combination products
- Drive continuous improvement initiatives across complaint processes, systems and team capabilities
- Bachelor’s degree in Engineering, Life Sciences, or a related field
- 5+ years of experience in Quality Assurance within the pharmaceutical, biotechnology, or medical device industries with at least 3 years’ experience focused on combination products complaints
- Strong understanding of post-market surveillance, global safety reporting and regulatory requirements for combination products, including FDA, EMA, and other health authority guidelines.
- Strong understanding of ISO 13485, ISO 14971, QMSR, Part 4, and other relevant standards.
- Proven track record in leading cross-functional teams
- Excellent communication, leadership, and problem-solving skills.
- Experience in building and scaling global complaint handling systems
- Proficiency with electronic systems (e.g. Trackwise) and tools for handling complaints
- Experience integrating complaint and safety data into product lifecycle and risk management strategies
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.Employee Status: RegularRelocation: No relocationVISA Sponsorship: NoTravel Requirements: 10%Flexible Work Arrangements: HybridShift: Not IndicatedValid Driving License: NoHazardous Material(s): N/AJob Posting End Date: 05/16/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Expected salary:
Location: Rahway, NJ
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