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  • Quality Manager

    Alhambra • Permanent • Featured Job

    My client is looking for a Quality Manager that implement the quality standards of the Group. This position reports directly to the Group Technical Director and will have total support from the Headquarters.

    • Quality Systems, ISO 9001, Audits
    • Safety, Process, 5S, CAPA
  • Quality Engineer

    Pittsburgh • Permanent

    The ideal candidate will report to the Director, Global Quality Assurance with a dotted line to the Director of Manufacturing North America and is the site Management Representative regarding all ISO 9001:2008 activity at two facilities.

    • Global Manufacturing Company
    • Exponential room for career growth!
  • Regulatory Affairs - Medical Device - Relocation to FL

    Boston • USD70,000 - USD85,000 • Permanent

    Our client is a leading OEM medical device company with locations throughout Europe and the US. With a wide array of medical device products mostly with electro-mechanical components, they have an open position to join a growing team in Largo, FL for a Regulatory Affairs Specialist with experience working on medical device submissions and domestic policies.

    This position sits in Largo, FL. Relocation assistance provided.

    • Relocation to Largo, FL for this position
    • 510k submissions experience required; Medical Device product experience required
  • Quality Engineer- Medical Device

    Billerica • USD80,000 - USD100,000 • Permanent

    This position will play a key role with continuously improving the organization's Quality Management Systems in accordance with the ISO and FDA regulations. Additionally, the QE will drive product quality to meet the satisfaction of customers.

    • Expansion position with a rising OEM medical device startup.
    • Excellent growth opportunity with visibility to Senior Leadership.
  • Medical Device Regulatory Affairs Specialist

    Largo • USD70,000 - USD85,000 • Permanent

    Our client is a leading OEM medical device company with locations throughout Europe and the US. With a wide array of medical device products mostly with electro-mechanical components, they have an open position to join a growing team in Largo, FL for a Regulatory Affairs Specialist with experience working on medical device submissions and domestic policies.

    • Domestic Affairs/Legal Affairs/Compliance/Regulations/ 510k Submissions
    • Medical Device experience required
  • Quality Assurance Manager

    Naperville • USD92,000 - USD118,000 • Permanent

    This organization owns the lion share of the custom made shortenings, oils, dressings, and sauces market for retail and foodservice industries. 2017 is expected to be another growth year for the business with strategic acquisition initiatives ahead.

    • #1 Producer of custom dressings and flavorings!
    • Opportunity to help shape the future of Quality Department!!
  • Quality Engineer - Aerospace Manufacturing

    Hartford • Permanent

    The quality engineer will provide statistical information for quality improvement by identifying testing methods and samples.

    • Exciting Quality Engineer opening with a Gloabal Aerospace Company.
    • BS Engineering, AS9100 experience required.
  • Quality Production Manager

    Springfield • USD75,000 - USD88,000 • Permanent

    Michael Page is partnering with a fast growing manufacturing company that services both the military and consumer sectors. In this family run business, there is an open position for a Quality Production Manager that will be highly visible within the organization.

    • Fast growing organization, ISO 9001 auditor certification highly preferred
    • Great employee culture
  • Quality Engineer

    Wrentham • USD65,000 - USD80,000 • Permanent



    This company is a contract manufacturing medical device company located near Wrentham, MA. While it is a smaller organization, the atmosphere is friendly and collaborative, and boasts a very strong learning environment. This company is quickly becoming well known for its top quality products.

    • Medical Device company - open to out of insdustry candidates
    • Local candidates Preferred
  • Quality Assurance Manager

    Tinley Park • USD84,000 - USD112,000 • Permanent

    The QA Manager will be leading the training, development, and overall strategy of the QA department. This cross-functional role reports to the plant manager and involves improving processes and implementing corporate quality assurance policies. This is a highly visible position in the organization, where you will become the in-house subject matter expert and mentor a lean team.

    • Become the subject matter expert with a global food manufacturer at a key site.
    • Utilize your technical expertise and leadership qualities for a young QA dept.
  • Regulatory Affairs Manager - OEM Medical Device

    Minneapolis • USD110,000 - USD135,000 • Permanent

    Michael Page is partnering with an OEM Medical device company west of Boston. Though already well established with sites around the world, they have strong growth projections over the next few years. This company manufactures and sells multiple product lines that typically have an electronic or surgical application, and are continuing to bring new products out to market every year.

    *Relocation to MA provided as position is located in Marlborough, MA

    • OEM Medical device company - Relocation to Marlborough, MA
    • 510k submissions experience; hands on and strategic role
  • Quality Manager

    San Diego • Permanent

    In this role you will be responsible for managing the day-to-day quality and compliance activities for my client, and related manufacturing, packing and storage sites. You will oversee and ensure compliance of these products to the Product Specifications, as well as GMP or other relevant regulatory or industry requirements. Manage the release activities, OOS, deviations, complaints, and investigations provided by contract manufacturers. Ensure adherence of contract manufacturers to the Quality Agreements and manage the relationships with them, including change control. Manage the specification review and approval processes, and support specification review and approval. Manage any other technical documentation required for products, and oversee the ongoing stability program.

    • Nutraceuticals, F&B, Quality
    • QSM, Quality System, ISO
  • Product Steward/Regulatory Specialist

    Houston • USD85,000 - USD100,000 • Permanent

    Monitor total quality of client's products at all levels of supply chain including transportation, distribution and store level. Experienced in Federal, State and Local registration for cleaning products. Compliance experience is a must! Understanding of the EPA regulation for transportation compliance and import regulations is preferred.

    • Exciting product stewardship role with a global CPG brand in Houston!
    • Quality/Regulatory Compliance, leader needed in a growing international company!
  • Quality Assurance Engineer

    Providence • USD70,000 - USD95,000 • Permanent

    Working with a manufacturing company that produces components and fixtures for electro-mechanical industry as well as the aerospace and defense industry. This is a great opportunity to join a dynamic team as a Quality Assurance Engineer and grow within the company.

    • Growing manufacturing company with upward career progression
    • Engineering Degree Required
  • Quality Assurance Manager

    Somerset • USD80,000 - USD110,000 • Permanent

    Our client is a Privately-Held manufacturer of injection molded rigid plastic caps that is seeking a Quality Assurance Manager

    • Privately-Held manufacturer of injection molded rigid plastic caps
    • Excellent career opportunity with a growing company
  • Quality Engineer

    Danbury • Permanent

    Leading contract manufacturer serving the medical, commercial, and aerospace industries, seeking a Quality engineer to help develop and implement quality improvements and lean initiatives.

    • Exciting opportunity for Quality Engineer*- great growth potential
    • Leading manufacturer seeking Quality Engineer!
  • Senior Quality Engineering Manager

    Danbury • Permanent

    Our client is seeking a Senior Quality Engineering Manager to lead and develop a Quality Engineering team responsible for operations quality, design changes, and transfer projects. The manager will be responsible for developing, establishing and maintaining quality assurance programs, policies, processes, procedures and controls ensuring that performance and quality of products conform to established requirements, standards and agency regulations.

    • A leading medical device manufacturing company located near Danbury, CT
    • Hiring a Senior Quality Engineering Manager with prior industry experience
  • Quality Engineer - Plastics

    Elmhurst • USD76,000 - USD92,000 • Permanent

    Serve as a Quality Engineer for an organization specializing in plastic parts design for large automotive, appliance, and industrial manufacturers. Take on new special testing challenges with an organization experiencing steady growth and providing multiple career paths.

    • Lead the Quality team, enhancing multi-site organizational metrics
    • Leverage the latest molding technologies with a global plastic parts company
  • Quality Engineer and Supervisor

    Dover • Permanent

    Global manufacturing company, seeking a Quality Engineer/ Supervisor to join their team!

    • Global Manufacturing Company
    • Exponential room for career growth!
  • Quality Assurance Manager - ISO13485

    Marlborough • USD100,000 - USD125,000 • Permanent

    Michael Page is partnering with an OEM Medical device company west of Boston. Though already well established with sites around the world, they have strong growth projections over the next few years. Due to growth and new vision, they have an immediate opening for a Quality Assurance Manager.

    • ISO 13485 and Electrical Background required
    • Engineering Degree for high level quality leadership role
  • Quality Engineering Manager - ISO13485

    Westborough • Permanent

    Michael Page is partnering with a small medical device company that has been making a lot of headway in the manufacturing industry. Due to restructuring, a new position for a Quality Engineering Manager has arisen. This company is on the rise and looking to bring in a technically savvy manager to help lead the quality group.

    • OEM Medical Device Company
    • ISO13485 experience required; BS in Engineering Required
  • Director of Quality and Regulatory - Medical Device

    Marlborough • USD140,000 - USD170,000 • Permanent

    Michael Page is partnering with a medical device company that is in a resurgent phase within their quality and regulatory department. With a brand name that has a good reputation in the market, the Director of Quality and Regulatory - Medical Device will have the opportunity to be a change agent and reinvigorate the market.

    • Must have experience in director level capacity with QA/RA ISO13485
    • Multi-site responsibility
  • Senior Quality Engineer - TS16949

    Norwood • Permanent

    Michael Page is partnering with a manufacturing organization just outside of Boston who have a new opening for a Senior Quality Engineer - TS16949. This opportunity is newly created due to growth within the organization and potential growth the company expects to have over the next coming years. This is an individual contributor role that has a lot of visibility to upper management and a lot of opportunity to become a leader within the organization. Micha

    • Automotive TS 16949 experience required
    • Well established manufacturing company well positioned for continued growth
  • Quality Assurance Engineer - Medical Device

    Framingham • USD70,000 - USD100,000 • Permanent

    The Quality Assurance Engineer is responsible for the maintenance and improvement of the Quality System according to FDA, ISO and other relations regulations and requirements.

    • Exciting Quality Engineer position with a rising provider in Framingham.
    • This client manufactures infusion pumps for the medical device industry.
  • Quality Control Supervisor

    Hartford • Permanent

    Accomplish strategic objectives by overseeing and performing multiple project activities in achieving Quality Assurance Standards

    • Established and Growing food production facility
    • Excellent opportunity for growth