At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world’s top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.
JOB SUMMARY
This position has the responsibility and authority to lead assigned Quality System processes. In addition this role will lead internal audits, customer audits, ISO Registration audits, FDA Inspections and when required prepare submissions and responses to FDA and ISO Registrars. This position will serve as the primary contact for site departments, business units, and corporate functions and will work closely with direct reports to provide guidance and development opportunities.
ESSENTIAL DUTIES AND RESPONSIBILITIES
· Be the Champion and subject matter expert for the Quality Systems and Compliance programs.
· Ensure the site’s quality system development, effective maintenance and continued compliance with business unit requirements, medical device regulations and standards (i.e., U.S. – FDA, ISO 13485, ISO 9001)
· Lead department activities within the Quality Systems function (i.e., Document and Data Control, Retain and Records Retention, Training, Corrective and Preventive Action, Change Control, Deviation, Supplier Audits, Supplier Corrective Action Requests, Electronic System Development/Validation, Management Review, Risk Management, Auditing, Agency Inspections and Quality Improvement Initiatives)
· Ensure the accuracy of the regulatory contact and submission log is maintained; provide regulatory guidance to various internal project teams as necessary.
· Lead the follow-up, negotiation and resolution of issues regarding current and future submissions with appropriate regulatory agencies and ISO registrars.
· Continue to develop and enhance current regulatory knowledge at both the local and national levels to support surveillance activities.
· Lead the support of currently marketed products including review of engineering changes, labeling, promotional material, product chances and documentation of changes requiring government approval.
· Responsible for proposing and execution of Quality System improvement opportunities, and developing and maintaining Business Continuity Planning programs.
· Responsible for writing, reviewing and approving validations in accordance with customer and regulatory requirements.
· Establish, maintain and report Quality System metrics to local level teams, management and global business units.
· Ensure timely and comprehensive closure of systems, including adherence to all in-process milestones. Facilitate prioritization and resource discussions with Change/Improve and other stakeholders.
· Support the effectiveness of the Quality Systems and Compliance programs by working collaboratively with other stakeholders to ensure effective and compliant processes.
· Manage expenses; provide support to budget planning, scheduling, and site wide process improvement opportunities.
· Perform all duties in alignment with the Jabil Corporate Code of Ethics, Corporate and Global policies, Employment Labor Laws, Health Regulatory Agency Regulations, and Safety Requirements
· Other duties as assigned
JOB QUALIFICATIONS
KNOWLEDGE REQUIREMENTS
· Knowledge of the U.S. and international medical device quality system regulations, standards and best practices (21 CFR 820, ISO 13485)
· Some experience with compliance assessments, gap assessments and risk management assessments.
· Experience with program change management practices, lean or six sigma, program and system integration efforts
· Strong computer skills; Word, Excel, PowerPoint
· Strong interpersonal skills are required. Must be an effective team player intra-departmentally and cross-functionally.
· Strong leadership, collaboration and relationship building skills. Must be able to work in a team environment, influence change without alienating others.
· Must have a high tolerance for ambiguity
EDUCATION & EXPERIENCE REQUIREMENTS
· Bachelor’s degree required (Quality, Regulatory, Engineering, Business or Life Sciences)
· Master’s degree is desired (Quality, Regulatory)
· 6 + years of industry experience within Quality and/or Regulatory, and managing high performing teams.
· American Society of Quality, Certified Quality Auditor (CQA) credentials, is required.
· Regulatory Affairs Professional Society (RAPS) Certification is desired.
· Or a combination of education, experience and/or training.
JOB SUMMARY This position has the responsibility and authority to lead assigned Quality System processes. In addition, this role will lead internal audits, customer audits, ISO Registration audits. This position will serve as the primary contact for site departments, business units, and corporate functions and will work closely with direct reports to provide guidance and development opportunities.
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Be the Champion and subject matter expert for the Quality Systems and Compliance programs.
- Ensure the site’s quality system development, effective maintenance and continued compliance with business unit requirements, medical device regulations and standards (i.e., ISO 9100, ISO 17025, ISO 14001, ISO 45001 ANSI ESD s20.20)
- Lead department activities within the Quality Systems function (i.e., Document and Data Control, Retain and Records Retention, Training, Corrective and Preventive Action, Change Control, Deviation, Supplier Audits, Supplier Corrective Action Requests, Electronic System Development/Validation, Management Review, Risk Management, Auditing, Agency Inspections and Quality Improvement Initiatives)
- Ensure the accuracy of the regulatory contact and submission log is maintained; provide regulatory guidance to various internal project teams as necessary.
- Lead the follow-up, negotiation, and resolution of issues regarding current and future submissions with appropriate regulatory agencies and ISO registrars.
- Continue to develop and enhance current regulatory knowledge at both the local and national levels to support surveillance activities.
- Responsible for proposing and execution of Quality System improvement opportunities and developing and maintaining Business Continuity Planning programs.
- Responsible for writing, reviewing and approving validations in accordance with customer and regulatory requirements.
- Establish, maintain, and report Quality System metrics to local level teams, management, and global business units.
- Support the effectiveness of the Quality Systems and Compliance programs by working collaboratively with other stakeholders to ensure effective and compliant processes.
- Perform all duties in alignment with the Corporate Code of Ethics, Corporate and Global policies, Employment Labor Laws, Health Regulatory Agency Regulations, and Safety Requirements
- Strategy and Development - Contribute to the creation and implementation of best practice capacity planning vision, strategy, policies, processes and procedures to aid and improve operational performance
- Strategy and Development - Contribute to new business initiatives and projects and review and communicate the impact on Quality Management Systems (QMS)
- Conduct risk assessments of processes and tasks in the department
- Embed a culture of continuous improvement throughout the company
- Other duties as assigned.
JOB QUALIFICATIONS KNOWLEDGE REQUIREMENTS
- Experience with implementation of new quality management certifications
- Experience with compliance assessments, gap assessments and risk management assessments.
- Experience with program change management practices, lean or six sigma, program, and system integration efforts
- Strong computer skills; Word, Excel, PowerPoint
- Strong interpersonal skills are required. Must be an effective team player intra-departmentally and cross-functionally.
- Strong leadership, collaboration and relationship building skills. Must be able to work in a team environment, influence change without alienating others.
- Must have a high tolerance for ambiguity.
EDUCATION & EXPERIENCE REQUIREMENTS
- Bachelor’s degree required (Quality, Regulatory, Engineering, Business or Life Sciences)
- Master’s degree is desired (Quality, Regulatory)
- 6 + years of industry experience within Quality and/or Regulatory and managing high performing teams.
- American Society of Quality, Certified Quality Auditor (CQA) credentials, or equivalents required.
- Or a combination of education, experience and/or training
BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil.com e-mail address; direct phone call from a member of the Jabil team; or direct e-mail with a jabil.com e-mail address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number, birth certificate, financial institution, driver’s license number or passport information over the phone or via e-mail. If you believe you are a victim of identity theft, contact your local police department. Any scam job listings should be reported to whatever website it was posted in.
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 identity, 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
[email protected] with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.#whereyoubelong
