Medical Device Document Control Specialist | Quality
Life Spine
Life Spine is seeking a Document Control Specialist based in Huntley, Illinois. The role involves maintaining and creating compliant documents for training and auditing across departments. Responsibilities include managing document workflows, ensuring compliance, and performing document audits in a quality-driven environment. The ideal candidate should have a Bachelor’s degree and at least two years of experience in a quality environment, along with strong attention to detail and communication skills. #J-18808-Ljbffr Life Spine
- .... We are dedicated to improving the quality of life for patients by increasing procedural... ...solutions for spinal pathology. The Document Control Specialist is responsible to maintain, create,... .... Experience and knowledge of medical device Quality System Regulations and ISO...QualityMedical device
$95k - $110k
Supervisor, Quality Engineering Composed of Chromalox, Durex Industries... ...’ expertise in the thermal control business. A trusted custom... ...system requirements. Documentation Control: Develop and maintain... ....g., aerospace, automotive, medical device, or precision machining), with...QualityMedical deviceLocal area- ...Senior Document Control Coordinator Leading medical device company looking for an experienced Senior Document Control Coordinator. Ideal candidates should... ...a Bachelors degree with 36+ years of experience in quality systems, regulatory, or compliance roles within a regulated...QualityMedical deviceWork at officeFlexible hours
- ...By joining our Power Transmission and Distribution team as a Document Controller you will be responsible for establishing governance and... ...also be liaising with the DE Manager on BIM360 project level Quality Audit implementation, operation and record keeping for their...QualityFor subcontractorWork at officeWork from home
- ...the design and development of thermoformed medical packaging. This role involves... ...through CAD design and collaboration with quality teams. Ideal candidates will have a Bachelor... ...packaging design, preferably for medical devices. The position comes with competitive benefits...QualityMedical device
- ...firm is looking for an individual contributor with expertise in document management and technical writing. The role requires excellent... ...approach. The ideal candidate will have knowledge of document control processes and should be able to work independently. This position...
- ...previous experience. Expert in Microsoft word, technical writing, working with cross functional Excellent working knowledge of document control management processes and practices Ability to learn new concepts, coach, mentor, or train on new concepts. Strong...
- ...is seeking an Assembler to join their team. The ideal candidate will be responsible for the production of medical device components, ensuring adherence to quality standards while operating various equipment. The role requires excellent attention to detail, manual dexterity...QualityMedical deviceHourly payDay shift
- ...Lamination Operator at Technipaq is responsible for producing quality film consistently. They are able to manage the machine and... ...adhered to.Technipaq is family owned and operated serving the medical device and pharmaceutical packaging industry since 1984. We started...QualityMedical deviceShift work
- ...solutions for the food, beverage, medical and consumer goods industries... ...the healthcare and medical device industries. Our focus is on... ...collaboration with quality and regulatory teams, and proactive... ...production, functional testing, and documentation for IQ/OQ/PQ. Participate in...QualityMedical deviceLocal areaFlexible hours
$50 - $55 per hour
...Job Title: Quality Management Systems Specialist Location: Cary, Illinois... ...Overview Join a global medical technology... ...lead critical Change Control activities, collaborate... ...regulated medical device environment... ...are appropriately documented, assessed for impact...QualityMedical deviceContract workLocal areaRemote workFlexible hours- The Matlen Silver Group, Inc. is seeking a Regulatory & Quality Systems Specialist in Cary, IL. This contract role focuses on supporting regulatory compliance and quality initiatives for medical devices in the U.S. and internationally. Ideal candidates will have extensive...QualityMedical deviceContract work
- Design Engineer - Medical Packaging The Design Engineer... ...‑ready. Partner with Quality and Regulatory teams... ...preparation of IQ/OQ/PQ documentation. Participate in... ...packaging design; medical device or healthcare industry... ...angles, wall thickness control, and undercut design....QualityMedical device
- ...solutions company seeks a Manufacturing Associate in Crystal Lake, IL. Responsibilities include product inspection, machine operation, and quality checks in a clean zone environment. Candidates must have a High School Diploma or GED and be capable of lifting 45 lbs repetitively...QualityMedical devicePermanent employmentTemporary workFlexible hoursShift work
- ...managing the machine operations to produce quality film consistently. We offer a comprehensive benefits package, including medical, dental, vision, 401(k) with matching, paid... ...family-owned business serving the medical device and pharmaceutical packaging industry since...QualityMedical device
$85k - $100k
...development of thermoformed medical packaging products, transforming... ...collaboration with quality and regulatory teams, and proactive... ...production, functional testing, and documentation for IQ/OQ/PQ. Participate in... ...preference for medical device packaging. Proficiency with...QualityMedical devicePermanent employment- ...highly skilled Regulatory & Quality Systems Specialist to support regulatory... ...quality initiatives for medical devices, both in the U.S. and internationally... ...Purchasing and Supplier Controls Design & Development... ...and maintain technical documentation, including procedures and...QualityMedical deviceContract workWork at office
$52 - $55.87 per hour
...Staff Specialist, Quality Management Systems Hybrid in Cary, IL Pay: $55.87/... ...leading and owning the Change Control process within a regulated medical device environment. In this role, you... ...all changes are appropriately documented, assessed for impact, and effectively...QualityMedical deviceFull timeContract workFor contractorsWork at officeLocal areaShift work- ...solutions for the food, beverage, medical and consumer goods... ...requirements of the medical device and healthcare industries.... ...adherence to all safety and quality standards. Lead talent development... .... Oversee engineering documentation, change control processes and design...QualityMedical deviceLocal areaFlexible hours
$30 - $36 per hour
...Work Model: Onsite Overview Join a leading medical technology organization as a Sourcing... ...monitor supplier performance metrics to drive quality and efficiency. Lead and coordinate... ...industry, particularly within the Medical Device sector. Requirements 6+ years in Supply Management...QualityMedical deviceContract workLocal area$60 - $62 per hour
...Title: Sr. Regulatory Affairs Specialist Location: Cary IL 60013 Pay... ...Job Description: Job Title: Quality/Regulatory - Senior Staff... ..., preclinical, and clinical document for submission filing to comply... ...requirements for Class IIa medical device. Education / Work Experience...QualityMedical deviceContract workWork experience placementLocal area$58 - $64 per hour
...: Senior Regulatory Affairs Specialist Location: Cary, Illinois Type... ...Overview Join a leading medical device organization as a Regulatory... ...regulatory requirements for quality, preclinical, and clinical data... ..., preclinical, and clinical document for submission filing to comply...QualityMedical deviceContract workLocal area- ...operator and lead and is responsible for consistently producing quality printed material. The Press Lead also oversees the day-to-day... .... Technipaq is family owned and operated serving the medical device and pharmaceutical packaging industry since 1984. We started...QualityMedical deviceWork experience placementShift workDay shift
$30 - $36.83 per hour
...in assigned commodity. Obtains the best quality, service, and value for products and... ...identify and implement appropriate cost controls and business strategy changes. Perform... ...operating in a highly regulated industry. Medical Device industry sourcing and supplier...QualityMedical deviceHourly payContract work- Stryker is hiring a Senior Quality Engineer in Cary, IL to support... ...support quality assurance, control, and preventive activities... ...create and approve technical documentation. Lead basic root cause investigations... ...of pharmaceutical and/or medical device manufacturing processes....QualityMedical device
- Our client, a Global Medical Device Manufacture has an immediate opening for a Regulatory Affairs Specialist for a 12 Month + Contract . Our client... ...requirements for quality, preclinical, and clinical... ...preclinical, and clinical documents for submission filing to ensure...QualityMedical deviceContract workLocal areaImmediate start
- ...everything from industrial equipment and medical devices to consumer electronics and automotive... ...company focused on delivering high-quality products, responsive customer support,... ...activities simultaneously Maintain accurate documentation and order information Assist with...QualityMedical deviceWork at office
- ...company! Benefits ~ Medical, Dental, Vision and... ...design and production of medical devices. Apply today Hours: 1st... ...ensuring products meet established quality requirements.... ...practices. 2. Inspection and Documentation Perform visual inspection...QualityMedical deviceHourly payFull timeTemporary workSummer workLocal areaShift workDay shift
- ...from customers and evaluate potential quality issues. Develop and execute IQ, OQ, and... ...member. Process all stages of validation documents and oversee the completion and... ...regulated industry Working knowledge of Medical Device Regulations and Standards (FDA, ISO 134...QualityMedical deviceTemporary workDay shift
- ...Stand and walk for the full shift while maintaining focus on quality and throughput.Schedule2nd Shift (Cary Location): 2:00 pm - 1... ...TechnipaqWe’re a family‑owned manufacturer supporting critical medical device and pharmaceutical packaging. Since 1984, we’ve expanded from...QualityMedical deviceCasual workShift work
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