Medical Device GMP Technician I
Instylla
Instylla, Inc. in Bedford, MA seeks a Manufacturing Technician I to execute manufacturing activities including primary packaging, formulation and filling, and final packaging under SOP guidance. You will support multiple product lines from general packaging to formulation and filling processes in a controlled environment. The role requires 1–3 years in medical device manufacturing, ability to read and follow process docs, and strong attention to detail with good communication. #J-18808-Ljbffr Instylla
- ..., and validation initiatives for pharmaceutical, biotech, and medical device facilities in the New England region. The role requires directing... ..., engaging with clients, and ensuring on-time delivery in a GMP-compliant environment. Travel up to 100% is possible; the...Suggested
- ...commissioning, qualification, validation, and revalidation across facility, equipment, utilities, automation, cleaning, sterilization, medical device, and drug product processes. You will develop into a subject matter expert in process validation and cleaning/sterilization...Suggested
- LeMaitre Vascular is seeking an entry-level manufacturing associate to produce medical devices in an ISO Class 8 cleanroom environment. You will read and follow safety rules, specifications and instructions to assemble devices and perform quality checks. Ideal candidates...Suggested
- ...maintains project schedules and budgets. You will mentor commissioning and validation teams, contribute to proposals, and ensure adherence to cGMP standards for pharmaceutical, biotech, and medical device programs. #J-18808-Ljbffr IPS - Integrated Project Services, LLCSuggested
- Advantage Technical is seeking an Operations Quality Technician in Acton, MA, on a contract basis. In this role, you will support quality assurance within a medical device manufacturing environment, conducting inspections and maintaining quality documentation. The ideal...SuggestedContract work
- ...and other regulatory guidelines related to the manufacturing of medical devices.What You BringBachelor’s Degree in engineering or equivalent... ...of ISO 14971 Risk Management for Medical Devices.Knowledge of GMP/ISO requirements, specifically current ISO 13485 Medical Devices...Full timeImmediate start
$160k - $185k
...on X, LinkedIn and Facebook.Role Summary:The Senior Manager, GMP QA Operations oversees quality activities associated with contract... ...6+ years’ experience in related cGMP environment (e.g., Medical Device, Diagnostic, Pharmaceutical, or other similar regulated industry...Contract workWork experience placementLocal areaFlexible hours$175k - $200k
...Quality Systems, procedures, policies, and metrics supporting GMP activities. Provides leadership across QA operations while proactively... ...8+ years’ experience in related cGMP environment (e.g., Medical Device, Diagnostic, Pharmaceutical, or other similar regulated...Contract workWork experience placementLocal areaFlexible hours- NeuroBionics in Somerville, MA is hiring a Manufacturing Technician to build clinical-grade devices and support IO fiber production. You will perform high-skill assembly to spec, run inspections, maintain critical documentation, and support R&D prototypes when needed....
- ...engineer will be supporting the integration of a drug product with a medical device to produce a combination product. The position is set in a... ...clean room environment to support clinical studies.Understand GMP regulation and FDA/EMEA guidance on manufacturing processes...Full timeLocal area
- ...: Instylla, Inc. is a privately held medical device company based in Bedford, MA, focused on... ...We are seeking a hands-on Laboratory Technician to take ownership of Instylla's R&D lab.... ...strong plus. ~ Working knowledge of GDP, GMP, and ISO 13485 / 21 CFR 820 quality system...
$78k - $156k
...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000... ...a fast-paced, changing environment.Detailed knowledge of FDA, GMP, and ISO 13485.Apply NowLearn more about our health and wellness...Full timeWorldwideShift work- ...Description Job Description Equipment Technician / Engineer Onsite. Night Shift Available... ...Plant Maintenance, Construction, Oil and Gas, Medical Communications, Accounting, Finance, Electronics, Scientific, Medical Device, Sales, Pharmaceutical, Admin, Automation,...Night shift
- ...regulated environments, have over 10 years of relevant experience, and be able to optimize system performance while ensuring compliance with GMP standards. The role offers competitive compensation, including salary, bonus, and a full benefits package. #J-18808-Ljbffr Stanley...
$84k - $105k
...utilities, automation/computer systems, cleaning, sterilization, medical device, and drug product manufacturing processes. This role develops... ...for validation activities. Represents validation during site GMP activities and participates on cross-functional teams....Full timeImmediate start$102.5k - $125k
...engineering support for existing medical products as well as new... ...and/or provide direction to technicians; may train manufacturing personnel... ...13485, the Canadian Medical Devices Regulation (CMDR), Medical... ...required ~ Familiar with QSR / GMP regulations ~ Experience...Contract workWork at officeFlexible hours- ...OfficeLabControlled areasRequired QualificationsWorking knowledge of GMP, quality systems, and regulatory requirements.Experience... ...QualificationsExperience in pharmaceutical, biotech, medical device, or other regulated manufacturing environments.Familiarity with...
- ...and validation, manufacturing process development activities, product risk management requirements, and delivery. Requirements : Medical Device industry. 3+ years of experience. Complaint investigations. CAPA's. Evaluating nonconforming material. Experience with...
- Myomo, Inc. is seeking a Quality Inspector Technician in Burlington, MA to perform quality... ...candidate has 2+ years in electro-mechanical device quality inspection in the medical device field, familiarity with inspection tools and GMP/FDA practices, and a #J-18808-Ljbffr...
$26 - $28 per hour
...technology developed at MIT, Harvard Medical School and by the Company,... ...disabilities.) It is the only device that, sensing a patient’s own... ...of the Quality Inspector Technician role is to perform quality inspections... ...college may be a plus. FDA - GMP experience and training a plus...Full time$40 - $50 per hour
...of sterile drug production, radiopharmaceutical workflows, and medical device quality systems. Key Responsibilities: Provide day-to-day... ...applicable regulations, including 21 CFR Parts 210, 211, 820, EU GMP Annex 1, and radiation safety requirements. Support readiness...Hourly payPermanent employmentTemporary work$22 - $24.03 per hour
...Health & Wellness Comprehensive Medical, Dental, and Vision coverage Wellness... ...with barcode scanning systems and handheld devices Familiarity with inventory tracking... ...requirements Experience working in GMP, GLP, ISO, or other regulated environments...Hourly payFor contractorsWork at officeLocal areaMonday to FridayFlexible hoursShift work- ...manufacturing. The ideal candidate will have extensive experience in aseptic processing, strong technical leadership skills, and a commitment to GMP compliance. You will collaborate closely with engineering and manufacturing teams to successfully deliver projects while ensuring...Remote job
$152k - $228k
About MimecastMimecast started in email security — and we're still a recognized leader in it. But we're much more than that. Through strategic acquisitions and organic development, Mimecast has built a connected Human Risk Management platform that spans email security, ...Full timeWork at officeLocal areaWork from homeWorldwide- ...Mevion Medical Systems is looking for a Quality Control Inspector (Contractor) in Littleton, Massachusetts. The role involves ensuring that components meet quality standards through inspections and maintaining documentation. Ideal candidates have at least three years of...Contract workFor contractors
- ...standards. In this role, you serve as a subject matter expert in GMP quality systems, CMC quality oversight, and regulatory... ...transfer initiatives.• Thorough understanding of pharmaceutical and medical device Quality Management Systems.• Experience supporting regulatory...Full timeContract workImmediate start
- ...). Ensure compliance with FDA 21 CFR Part 820, ISO 13485, and GMP requirements. Maintain and update Quality Management System (QMS... ...'s degree in engineering or a related field. Experience in medical device manufacturing preferred. Strong understanding of regulatory and...
$27.46 - $43.94 per hour
...DESCRIPTION Job Title Quality Control Technician Job Description The Quality... ...GLP) and Good Manufacturing Practices (GMP). Your role: Supports the... ...requirements for good manufacturing controls for medical devices as outlined in quality control plans....Hourly payFull timeWork at officeImmediate startWork visaRelocation package3 days per week- ...Training, Leadership & InnovationTrain and mentor technicians, manufacturing personnel, and suppliers on... ...7-10 years of experience in the medical device industry and/or biomedical field preferredFamiliar with QSR / GMP regulationsExperience with Microsoft Office...Contract workWork at office
$38 - $47 per hour
...Job Title: Senior Electromechanical / Engineering Technician Location: Bedford, MA Location Type: Onsite Start Date: TBD... ...and communicative Industry-agnostic background welcome - no medical device experience required Nice-to-Haves: Experience with...Permanent employmentContract work
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