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JOB DESCRIPTION:
Johnson & Johnson is currently seeking a
POSITION SUMMARY
The Source Quality Engineer (Sr. SQE) provides overall quality assurance leadership in the management of Direct, Indirect Suppliers and/or External Manufacturers engaged in the production of Johnson and Johnson products. He/she leads the deployment of the Source Quality Management (SQM) strategies and associated standards, policies, procedures, programs, systems, processes, and initiatives for Ethicon Supply Chain Suppliers.
EXPERIENCE & EDUCATION
- A minimum of a Bachelor’s degree in Engineering, an Applied Science or a related technical and quality field is required.
- A minimum of 4 years of experience in a highly regulated industry is required.
- Prior manufacturing, plant or technical background is required.
- Working experience in good manufacturing practice regulated environment is preferred (medical device, pharmaceutical, etc.).
- Demonstrated knowledge of manufacturing principles and practices, and procedures.
- Direct experience in plant and/or supplier GMP auditing is preferred.
- Broad experience with quality systems, including but not limited to validation, non-conformance, CAPA systems and investigations, laboratory controls, production and process controls, is required.
- Experience with documentation and technical writing skills, in a regulated compliance environment, is required.
- Component Qualification/Process Validation experience is preferred. New product introduction experience is desired.
- Prior experience with FDA inspections is desirable.
- Broad knowledge of Quality System Regulations and Source Quality Management principles are desired.
- Demonstrated ability to identify compliance risks and assess business impact, is required.
- Ability to manage complexity and work in a diverse team environment is essential.
- Ability to deal with complex issues using deductive reasoning, critical analysis skills and systematic approaches.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
- Working knowledge of regulatory compliance requirements (i.e. Quality System Regulations (QSRs), Medical Device Directive (MDD), ISO 9001, ISO 13485, ISO 14971 or other international standards) required.
- Working knowledge of Quality issue investigation, Non-Conformance Reports (NCRs), Corrective and Preventative Actions (CAPAs) preferred.
- ASQ Certifications for Certified Quality Engineer (CQE), Quality Manager (CQM), and/or Supplier Quality Professional (CSQP) preferred.
- Quality Auditor qualifications or Lead Auditor certifications such as ASQ Certified Quality Auditor (CQA) or Biomedical Auditor (CBA) preferred.
- Flawless Project Execution (FPX) or Project Management Professional (PMP) trained and certified preferred.
- Six Sigma Black Belt/ Green Belt (CSSBB)/CSSGB) or Lean certification from a recognized program or PE leadership training preferred
- Strong analytical skills, metrics development and ability to identify trends are desirable.
- Knowledge of specific business practices and software applications skills (Word®, Excel®, PowerPoint®, Minitab®, Visio®, Microsoft Project®) is preferred
- Must have strong business acumen. The ability to collaborate with all levels of management in cross-functional team environment is required.
- Ability to communicate effectively in English.
- Bilingual in English and other language (Spanish, German, Portuguese, or Mandarin) is preferred.
ADDITIONAL POSITION REQUIREMENTS
- Personal protective equipment such as: Ear plugs, Safety Glasses, and Safety shoes.
- Ability to work in stressful/fast paced environment.
- Ability to work and interact with co-workers to accomplish company goals in a team environment.
- Management Skills.
- Analytical/Problem Solving Skills.
- Ability to communicate verbally and in writing.
- Ability to learn.
- This position may require up to 25% domestic and international travel.