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Jabil Regulatory Affairs Manager in Clinton, Massachusetts

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. With over 260,000 diverse, talented and dedicated employees across 100 locations in 30 countries, our vision is to be the most technologically advanced and trusted manufacturing solutions provider. We combine an unmatched breadth and depth of end-market experience, technical and design capabilities, manufacturing know-how, supply chain insights and global product management expertise to enable success for the world’s leading brands. We are driven by a common purpose to make a positive impact for each other, our communities, and the environment.

JOB SUMMARY

Act as focal point and subject-matter expert for all regulatory affairs activities. Participates in system and device product development teams to ensure regulatory, quality, and safety standards are incorporated into product specifications and manufacturing processes.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Acts as Regulatory liaison between the site and government agencies, authorized representatives and Notified Bodies.

  • Oversees and coordinates regulatory compliance aspects of product launch.

  • Provides fellow employees and customers with guidance and support to ensure compliance with regulatory standards and regulations.

  • Supports internal, external, and regulatory audits.

  • Leads development of regulatory training for the site.

  • Identifies and ensures compliance with all laws and regulations that apply to medical device manufacturers.

  • Recruit, lead, coach, manage, RA Department staff.

  • Collaborates with the customer and internal engineering teams to continuously improve regulatory compliance of the devices manufactured.

  • Works with customers and Business Units to create Regulatory, Quality, and Manufacturing plans providing clear, unambiguous, and mutual understanding of responsibilities and requirements for Jabil service(s) provided.

  • Works with design and process engineers to develop risk assessments.

  • Supports sales presentations, contract reviews, and quoting.

  • Participate in planning long term/short term functions of the department to support Jabil.

  • Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor.

  • Comply and follow all procedures within the company security policy.

  • May perform other duties and responsibilities as assigned.

    MANAGEMENT & SUPERVISORY RESPONSIBILITIES

  • Typically reports to Management. Direct supervisor job title(s) typically include: Senior Quality Assurance Manager.

  • Job is responsible for managing other employees (e.g., hiring/termination and/or pay decisions, performance management).

    JOB QUALIFICATIONS - KNOWLEDGE REQUIREMENTS

  • Ability to effectively present information and respond to questions from groups of managers, clients, and customers.

  • Ability to define problems, collect data, establish facts, and draw valid conclusions.

  • Ability to operate a personal computer including using a Windows based operating system and related software.

  • Advanced PC skills, including training and knowledge of Jabil’s software packages.

  • Ability to write complex correspondence. Read and understand visual aid.

  • Ability to apply common sense understanding to complete complex regulatory submissions.

  • Ability to deal with highly variable and fast-paced situations.

  • Ability to read and comprehend simple instructions, short correspondence, and memos.

    JOB QUALIFICATIONS - EDUCATION & EXPERIENCE REQUIREMENTS

  • Bachelor’s degree in relevant scientific, healthcare, engineering or other related field.

  • 5 to 8 years of progressive experience in the medical device industry with an emphasis in regulatory affairs, preferably in a medical device manufacturing environment.

  • Experience should include medical device safety and quality assurance, global regulatory affairs, and sterilization, as well as FDA audit experience, manufacturing, and Class I and II medical device experience.

  • Experience with private labeling a plus.

  • ISO 13485, MDD and QSR experience required.

  • Famliarity with MDR and CMDR.

  • Or an equivalent combination of education, training or experience.

    WORKING CONDITIONS

  • Regular business hours. Some additional hours may be required.

  • Travel requirements: Domestic and/or Global, up to 15%

  • Climate controlled office environment during normal business hours.

This job cannot be performed remotely in the state of Colorado.

Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identify, age, disability, genetic information, veteran status, or any other characteristic protected by law.

Accessibility Accommodation

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to Always_Accessible@Jabil.com or by calling 1.727.803.7515 with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to from this e-mail address and/or phone number.

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