Production Manager - GMP/ISO Medical Devices Lead Ops
$120k - $135kRegenity Biosciences
Regenity Biosciences in Oakland, New Jersey, is seeking a Production Manager to oversee daily manufacturing operations for medical devices and biomaterials. This role requires strong leadership to ensure compliance with GMP and ISO standards while driving a culture of safety and continuous improvement. The ideal candidate will have a Bachelor’s degree and 5+ years of leadership experience in a related field, along with excellent communication skills. A competitive salary range of $120,000 – $135,000 is offered. #J-18808-Ljbffr Regenity Biosciences
$120k - $135k
...Position Summary / Objectives The Production Manager is responsible for leading daily manufacturing operations for collagen-based medical devices and biomaterials in a regulated GMP/ISO 13485 environment consistent with Company’s policies and objectives. This role oversees...Medical deviceFull timeWork at office$100k - $120k
A recruitment firm is seeking a Production Manager to oversee operations in Paterson, NJ. The ideal candidate will plan daily production, manage labor and resources, and drive operational excellence. Required qualifications include a Bachelor's degree in Engineering and...SuggestedFull time- ...Franklin Lakes, New Jersey, USA, seeks a Site Quality Lead to drive compliance, CAPA leadership, audits,... ...site. The role requires 8+ years in medical devices or related industries and strong knowledge of 21CFR820, ISO 13485, MDD/MDR, and MDSAP. You will lead CAPA and...Medical device
$80.3k - $95k
A leading medical device company seeks a Quality Engineer in Mahwah, NJ. This role entails ensuring compliance with quality standards, managing cross-functional projects to meet FDA and ISO requirements, and developing the Quality Assurance Management System. Candidates...Medical device- ...Master Validation Reports, and lead PPAP/Validation activities for new... ...You will ensure compliance with GMP, ISO13485, and 21 CFR 820, write... ..., support APQP, DOE, FMEA, and manage change controls. A minimum of five years in a medical device quality role and a four-year engineering...Medical device
- ...procurement consultancy is seeking a Business Procurement Manager to enhance procurement strategies and supplier relationships... ...strategies. This role is based in Franklin Lakes, NJ, and focuses on supporting a leading Medical Device company. #J-18808-Ljbffr MillenniumSoft IncMedical device
- ...search for a Quality Systems Manager in Fairfield, New Jersey to oversee... ...focus on compliance with ISO standards and regulatory... ...have 10+ years of experience in medical device manufacturing, a strong understanding... ..., and the ability to lead teams effectively. Ownership...Medical device
- Getinge is seeking a Senior Manager of Regulatory Affairs in Wayne, New Jersey, to lead regulatory strategy and compliance... ...Workflows Infection Control Consumable products. This role involves... ...experience, deep knowledge of medical device regulations, and a strategic aptitude...Medical device
- A leading medical device company is seeking a Supplier Quality Specialist to oversee supplier management and quality assurance processes. This mid-senior level position requires experience in supplier qualification and compliance with Quality Management Systems. Responsibilities...Medical deviceContract work
- ...Franklin Lakes, NJ is seeking a Product Development professional to lead the development and... ...of packaging solutions for medical products. You will be responsible for managing cross-functional teams and... ...preferably within the medical device industry. The position requires...Medical device
- ...MedPharma is seeking a Quality Systems Manager for its Fairfield, NJ location. This role is critical in leading the Quality Management System in compliance with ISO 13485 and 21 CFR Part 820,... ...over 10 years of experience in medical device manufacturing and a proven track...Medical device
- A leading medical devices company is seeking a Senior Regulatory Affairs Specialist based in Franklin Lakes, NJ. In this role, you will manage regulatory strategies, ensure compliant documentation, and collaborate with various stakeholders for timely submissions in the...Medical deviceContract work
- ...policies and improve performance. This role requires a BS in Engineering or related field and at least eight years in medical device or related industries. You will coordinate with internal and external audits (FDA/ISO), manage CAPA board activities, and #J-18808-Ljbffr BDMedical device
- ...improvement of the Quality System, focusing on Supplier Quality Management. You will ensure compliance with regulations, manage supplier... ...in a quality assurance environment, preferably with FDA CFR or ISO knowledge and strong Excel skills. #J-18808-Ljbffr MillenniumSoft...
$40 - $45 per hour
...inspection, and testing of new product parts and assemblies.... ...using metric ANSI/ISO dimensioning and... ...document control systems in medical device and/or medical equipment... ...meet scheduled timelines (manage and coordinate tasks as... ...ISO 13485, ISO 7198 & GMP. Proficiency with...Medical deviceTemporary workFor contractorsImmediate start- ...Description The Principal, Medical Affairs role provides... ...support for designated product platforms - integrating... ...and delivery Lead the design, execution,... ...Ensure alignment with risk management and product safety considerations... ...experience in medical device or biotechnology...Medical deviceRemote jobWork at office
- Cibo Vita in Totowa, NJ, is seeking a Production Supervisor to oversee daily... ...manufacturing plant. The role involves managing staff, ensuring adherence to quality... ...manufacturing, and a strong understanding of GMP. Benefits include medical, dental, and vision coverage, life...
- ...2 years of experience in quality inspection, preferably within the pharmaceutical, biotech, or medical device industries. Key responsibilities include conducting 100% visual inspections and ensuring compliance with GMP standards. #J-18808-Ljbffr Discover InternationalMedical deviceContract work
- A medical device company is seeking a Supplier Quality Engineer to assist with ongoing business. This role requires a... ...Engineering, and familiarity with process validations and ISO regulations. Responsibilities include managing supplier change requests, ensuring compliance, and...Medical deviceContract work
- ...months. The ideal candidate will have 4-5 years of experience in medical device packaging and will be responsible for designing, prototyping,... ...or a relatable field, along with knowledge of relevant ISO standards and effective communication skills. The position involves...Medical deviceContract work
- ...Overview: Role: Lead Quality Engineer - Medical Devices & Compliance Location: Franklin Lakes, NJ... ...manufacturing. • Ensure compliance with FDA, ISO 13485, and other relevant... ...Design History Files (DHF), o risk management files and test protocols. • Provide...Medical device
- ...techniques Experience with polymeric product manufacturing processes preferred Experience... ...development teams, in the area of medical devices is preferred Technical writing... ...reports in a manner consistent with QSR, ISO, and GMP guidelines Experience with laboratory...Medical deviceContract work
$130k - $160k
...forward. As a global medical technology leader... ...a Zimmer Biomet product or technology every... ...leader and Management Representative responsible... ...a medical device design and manufacturing... ...requirements (QMSR, GMP, ISO, and other global... ..., mentor, and lead a high-performing...Medical deviceHourly payWork experience placementFlexible hours- ...Our customer is a global medical device company. The company is hiring... ...with DFM/A, GD&T, metric ANSI/ISO drafting standards, and statistical... ...: ISO 13485, ISO 7198, and GMP Skilled in documentation... ...Scrum and Waterfall project management methods Proficiency in Microsoft...Medical deviceTemporary workWork at office
- Position Packaging Engineer (Must Have Medical Device Packaging) Location Franklin Lakes, NJ Duration 1... ...experiments. Knowledge of the following standards: ISO 13485, ISO 11607, ISO 14971, EU MDR. Accountability Will not manage any direct reports. Will not be responsible...Medical deviceContract workFor contractorsH1bFlexible hoursShift workDay shift
- ...NJ, is looking for a Quality Systems Manager to join their team. This role involves leading the Quality Management System in alignment with ISO 13485 and FDA regulations, ensuring compliance... ...have over 10 years of experience in medical device quality systems and proven success...Medical device
- Product Test Engineer - Req Instron Mechanical Testing & Medical Device Industry Exp Join to apply for the Product Test Engineer - Req... ...conflicts and other issues to management in a timely manner. Maintains... .... Knowledge of GLP, cGMP, ISO, and ASTM methodologies beneficial...Medical deviceContract workShift workDay shift
- Position Packaging Engineer - Must Have Medical Device Packaging Exp Location Franklin Lakes, NJ Duration 6 Months... .... Knowledge of the following standards: ISO 11607, ISO 13485, ISO 14971 Accountability Will not manage any direct reports. Will not be responsible for...Medical deviceContract workFor contractorsWork at officeWork from homeRelocationFlexible hoursShift workDay shift
- Position Packaging Engineer (Medical Device packaging) Location Franklin Lakes, NJ (presence on-site; more after... .... Knowledge of the following standards: ISO 11607, ISO 13485, ISO 14971 Accountability Will not manage any direct reports. Will not be responsible for...Medical deviceContract workFor contractorsH1bFlexible hoursShift workDay shift
- ...packaging equipment in a GMP-regulated manufacturing environment... ...and reliably to support production schedules while... ...biotechnology, pharmaceutical, medical device, food, beverage, or ISO 13485 regulated... ...Computerized Maintenance Management Systems (CMMS). Ability...Medical deviceShift work
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