Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- An excellent retirement savings plan with high employer contribution
- Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
MAIN PURPOSE OF THE ROLE
Individual contributor with comprehensive knowledge of materials, chemicals, and product stewardship regulations who evaluates materials used in cardiovascular medical devices and manufacturing processes to ensure compliance with global regulatory requirements (EU REACH, EPR, RoHS, POPs, Stockholm Convention, Conflict Minerals, etc.) Acts as a technical subject matter expert in material composition, restricted substances, and supply chain compliance while supporting divisional Product Stewardship programs. Supports Product Stewardship team and under the direction of manager or supervisor while independently working and solving day-to-day problems. The function acts as a source of expertise within the division regarding product and chemical regulations and maintains a divisional program with clear program elements.
MAIN RESPONSIBILITIES
Compliance
- Comply with all regulations and procedures in scope of the Product Stewardship program.
- Ensures compliance with Product Stewardship requirements through internal processes and implementation of strategies.
- Maintain advanced knowledge of company and global regulatory activities to ensure effective Product Stewardship compliance.
- Track company, industry, and developing regulatory activities to ensure effective Product Stewardship compliance.
Organizational Interface
- Supports the Product Stewardship team and works under the direction of the manager while independently solving day-to-day problems.
- Evaluate materials used in products against regulation requirements based on their intended uses.
- Prepares and reviews written communication.
- Conveys information effectively through formal and informal documents and meetings.
- Exhibit advanced ability to apply concepts of careful communication.
- Following through on goals and incorporates the ideas of others; shares resources, insight, and accountability to benefit the objectives of the business.
Technical
- Evaluate material and chemical compositions against global product stewardship regulations.
- Assess supplier material disclosures, FMDs, IPC-1752A declarations, and substance compliance documentation.
- Review polymers, metals, coatings, adhesives, inks, and electronic component materials for regulatory impacts.
- Partner with R&D during material selection and design changes to identify product stewardship risks.
- Support material risk assessments related to REACH SVHC, RoHS, PFAS, POPs, California Proposition 65, and emerging regulations.
- Provide technical guidance on material substitutions and compliance strategies.
- Build relationships and coordinate data collection from suppliers and TPMs (e.g., Product composition, Conflict Minerals form, Compliance declarations).
- Support the affiliates with Extended Producer Responsibility reporting
- Identify emerging regulations or new requirements impacting division products; if needed, communicate to the other division functions and ensure actions are put in place.
- Execute a Product Stewardship program that includes division-specific requirements and is aligned with division priorities.
Problem Solving / Innovation
- Address internal and external stakeholders’ needs.
- Explore multiple alternatives to meet the requirements.
- Develop solutions for complex problems when necessary; integrates regulatory and operational needs.
- Leverage expertise to quickly enact tactical decisions and develop strategic plans.
QUALIFICATIONS
Education
Required:
- Bachelor's degree in Materials Science, Chemical Engineering, Materials Engineering, Mechanical Engineering, Environmental Engineering, Chemistry, or related scientific discipline.
Preferred:
- Advanced degree in Materials Science, Materials Engineering, Mechanical Engineering or related scientific discipline
Experience
- Minimum 4 years of relevant experience
- Ability to navigate and interpret medical device product stewardship regulations.
- Expected to function with little direction and be able to independently drive complex projects to completion.
- Ability to successfully manage multiple projects and daily responsibilities.
- Experience working in a broader enterprise/cross-division business unit model preferred.
- Ability to work in a highly matrixed and geographically diverse business environment.
- Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
- Ability to leverage and/or engage others to accomplish projects.
- Strong verbal and written communications.
- Multitasks, prioritizes and meets deadlines in timely manner.
- Strong organizational and follow-up skills, as well as attention to detail.
The base pay for this position is
$90,000.00 – $180,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Engineering
DIVISION:
CRM Cardiac Rhythm Management
LOCATION:
United States > Sylmar : 15900 Valley View Court
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 5 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Work in a clean room environment
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf