Quality Control Inspector I — ISO 9001 Medical Devices
Repligen
Repligen in Hopkinton, MA is seeking a QC Inspector I to actively participate in the ISO 9001 Quality Management System and inspect in-process and final assemblies of single-use parts at our Hopkinton facility. You will use visual inspection and measuring tools to ensure conformance with internal and customer quality standards. The role emphasizes integrity, compliance, and collaboration as part of our leadership behaviors. #J-18808-Ljbffr Repligen
- Repligen Corporation seeks a QC Inspector I at its Hopkinton, MA facility to perform in-process and final inspections of single-use assemblies... ...diploma or a two-year technical degree, familiarity with ISO 9001, and proficiency with basic Microsoft Office tools. #J-18808-...SuggestedWork at office
$24 - $30 per hour
...actively participate in the Repligen ISO 9001 Quality Management System. This role is responsible... ...—in all aspects of work. The QC Inspector I will be responsible for: Conduct... ...field will be considered. Familiar with medical devices, bioprocessing equipment, military or...Medical deviceHourly payWork at officeWorldwideFlexible hours- Role: QC Inspector I responsible for inspection, auditing, and reporting on in-process... ...facility, ensuring conformance to quality standards within ISO 9001. Responsibilities: conduct... ...9001 environment; familiarity with medical device or bioprocessing inspection standards...Medical deviceWork at office
$24 - $30 per hour
...Repligen seeks a Quality Control Inspector to conduct inspections and audits of single-use assembly... ...continuous improvement within an ISO 9001 certified system. Responsibilities... ...Outlook, Excel, Word) ~ Experience in medical device, bioprocessing, military, or...Medical deviceWork at office- Repligen seeks a QC Inspector I to perform in-process and final inspections of single-use assembly parts at our Hopkinton, MA facility.... ...labeling, document results, and flag non-conformities to uphold quality standards in a regulated environment. Responsibilities include...Suggested
- ...of laser technologies. IPG Medical, a wholly owned subsidiary of... ...to develop innovative medical device laser solutions that make the... ...documentation practices Assist Quality Engineers and manufacturing... ...and Excel. ~ Understanding of ISO 13485, ISO 14644, and CFR 21-8...Medical deviceFor contractors
$100k
Senior Quality Engineer Location: Devens, MA Job Type: Direct Hire / Full-Time Salary: $100,000, annually Industry: Medical Device / Regulated Manufacturing Lead Quality. Drive Compliance.... ...medical devices, FDA regulations, ISO standards, process validation,...Medical deviceFull timeTemporary workLocal area$24 - $35 per hour
...industries. We're looking for a Quality Inspector who takes pride in catching... ...System in accordance with ISO and/or AS quality standards.... .... Familiarity with ISO 9001 and/or AS9100 standards preferred... ...Benefits package (medical, dental, vision, 401k, etc.)...Permanent employment$98.06k - $135.36k
...Life, by advancing medical technologies and elevating... ...Senior Supplier Quality Engineer is... ...receiving site. Guides inspectors regarding incoming... ...(i.e., FDA, ISO / MDSAP). Supports... ...preferably in medical device or related Industry... ...and methods. ~ ISO 9001 / 13485/ FDA /...Medical deviceFull timeLocal areaWorldwide$101.6k - $158.8k
...successful implementation of Hologic’s connected medical devices and software. This role partners heavily... ...Services, Field Service, R&D and Quality. Digital Project Engineers play a key... ...comply with all applicable FDA regulations, ISO requirements, company policies, and...Medical deviceRemote workWork from homeFlexible hours- ...priorities effectively• Familiarity with ISO, FDA and other regulatory... ...tools• Demonstrated experience/knowledge of Quality Management System related tools• Demonstrated... ...Demonstrated experience with regulations in the Medical Device and/or Pharmaceutical industries•...Medical deviceLocal area
$80k - $85k
...TekniPlex is hiring a Quality Engineer for our Ashland... ...with customer, internal, ISO, GMP, and applicable... ...corrective actions, document control, change management,... ...with ISO 13485, ISO 9001, GMP, and applicable FDA... ...requirements (21 CFR); medical device and/or pharmaceutical packaging...Medical deviceDaily paidTemporary workFor contractorsLocal areaImmediate startFlexible hoursShift work$20 - $25 per hour
...Quality Technician $20-$25 Summary: The Quality Control Technician will work with Operations, Quality and Engineering... ...-4 years of previous quality inspector experience. ~ IPC 600 and 6... ...a plus ~ Experience with medical devices and/or ISO 13485 is a plus. ~...Medical deviceContract workWork experience placementWork at office$110k - $125k
Senior Manager, Contamination Control & Sterility Assurance (CCSA)... ...operational excellence, and strong quality performance across the... ...pharmaceutical, biotechnology, medical device, or other regulated life... ...sterilization, sterilization validation, ISO 11137, ISO 11737,...Medical deviceFull time$150k - $205k
...develop cutting-edge software for medical devices. With projects focused on... ...and process risk models from ISO 14971. Requirements... ...IEC 60601-1, IEC 60601-1-8. Quality & Process: 21 CFR Part 820, IEC... ...Deep understanding of design controls, software lifecycle coaching,...Medical device- ...America is a global leader in medical technology and advanced... ...innovations, smart instruments and devices, integrated ecosystems, and... ..., while producing high-quality components that support life... .... Knowledge of GMP, FDA, ISO 13485, or ISO 9001 manufacturing requirements....Medical deviceFull timeWorldwideMonday to FridayShift work
- ...Supplier Quality Engineer Web Industries, a 100% employee-owned... ..., including review of control plans, PFMEAs, process capability... ..., aerospace, defense, medical device, or another highly regulated... ...standards such as IATF 16949, ISO 9001, AS9100, ISO 13485, or related...Medical devicePermanent employmentWork at office
- ...customers to assure best-in-class quality for product and provide... ...and execution of Control Plans. Review device history records for quality... ...orientation. Experience in ISO-13485 certified required and... ...professional experience in medical subassembly and finished device...Medical deviceWork at office
$90k - $110k
...services, all with a Time to Market at WARP SPEED™ mindset - ensuring speed, quality, and flawless execution. Cogmedix is an FDA-registered, ISO 13485–certified partner for medical device innovators, specializing in complex electromechanical, laser, and electro-optical...Medical deviceContract work- ...America is a global leader in medical technology and advanced... ...innovations, smart instruments and devices, integrated ecosystems, and... ...to manufacture high-quality medical device components.... ...Quality System Regulations, ISO 13485, and ISO 9001 requirements. What Will...Medical deviceFull timeWorldwideMonday to FridayShift workDay shift
- ...America is a global leader in medical technology and advanced... ...innovations, smart instruments and devices, integrated ecosystems, and... ...through innovation, quality, and precision. About the... ...System Regulations, ISO 13485, and ISO 9001 standards. What Will Make...Medical deviceFull timeWorldwideMonday to FridayShift workNight shiftAfternoon shift
$26.15 - $33.27 per hour
...machinists produce precision components for medical devices used in operating rooms and surgery... ...in a regulated environment, so quality and documentation matter as much as cycle... ...components. Knowledge of GMP, FDA, ISO 13485 or ISO 9001 manufacturing requirements....Medical deviceHourly payFull timeWorldwideShift workDay shift$100k - $140k
...generation RF, microwave, medical, and specialty cable products... ...Engineering, Operations, Quality, and Equipment Development... ...input for machine control systems, automation strategies... ...process controls.Experience in ISO 9001, AS9100, or medical device quality environments.For...Medical deviceTemporary workFlexible hours- ...Description Job Description Quality Engineer II (Contract)... ...management. Apply design control and validation principles to... ...investigations. Familiarity with ISO 9001 or comparable quality... ...biotechnology, pharmaceutical, medical device, or life sciences...Medical deviceContract work
- ...Manufacturing Team Member in Hudson, MA. This temporary role involves basic assembly and inspection work following written procedures to meet quality and production standards. The position supports a wire rack and coatings workflow, with opportunities to grow within a global...Medical deviceTemporary work
- ...Supplier Quality Engineer Marlborough, MA Long Term Contract Supplier Quality... ...as a supplier quality engineer in the medical device industry • Experience in process validations... ...components of production and process controls including, IQ, OQ, PQ, PPQ,...Medical deviceLong term contract
$137.66k - $192.72k
...to Life, by advancing medical technologies and elevating... ...and are compliant with Quality System Regulations.... ...documentation according to ISO and GMP guidelines,... ...activities of the Design Control process. All activities... ...under Medical Device Regulations. Experience...Medical deviceFull timeLocal areaWorldwide- ...Job Title Manufacture medical products (capital equipment) by following... ...) years' experience in medical device development. Experience... ...capital equipment. Knowledge of Quality Systems. Experience with Medical Device Regulation ISO 13485. Experience working in...Medical deviceWork experience placement
- ...development by ensuring that design controls, verification and validation,... ...development and on-market medical devices.Facilitate application of... ...implementation.KnowledgeFDA Quality System Regulations, especially... ...Design Control requirements.ISO 13485 and Medical Device Directive...Medical device
$31 - $38 per hour
...Quality Control Analyst II The Quality Control Analyst II role is responsible for performing environmental monitoring... ...evaluations in accordance with approved SOPs, ISO 14644 cleanroom controls, and the company's ISO 9001 Quality Management System. The Quality...Hourly payWork experience placementWorldwideFlexible hours
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