Engineer, Supplier Quality II
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Heredia, Heredia Province
- Operations
- Hybrid
- Full-time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Support and follow up the suppliers to ensure that quality relevant materials and services meet
specifications and Company requirements.
Keep approved suppliers in compliance and document the entire process to meet the requirements of
regulatory agencies and QMR03 Supplier Controls policy.
Coordinate with other areas of the Company to comply with the procedures and goals established in the
area.
- Open, notify and track progress SCARs (supply corrective actions) to suppliers. Approve the corrective actions from the supplier and confirm with submitted evidence that committed activities were met
- Notify “alerts” to suppliers based on trend analysis, supplier metrics (supplier performance) or defects found during manufacturing or complaints processes. Perform follow-up of supplier notice alert, when needed.
- Track blocked, on hold and quarantine materials to determine a material disposition to comply with
the business goals or metrics. Define and execute material disposition of non-conforming materials. - Update and review the supplier metrics which show the quality performance of local and global
suppliers. Present monthly data to management. - Encourage suppliers to comply with periodic review and maintenance requirements for supplier
qualification such as “Quality Agreements (QTA)”, quality questionnaires (survey or self-assessment,
QQ), supplier audit, Supply chain maps, change notification, etc. Coordinate with the supplier the
completion and submission of QQ, QTA and material documentation. - Support and track the annual schedule of supplier audits (on site or quality questionnaire) to assure
that they are executed and completed on time. Present monthly status or supplier audit results to
management. - Provide corporate auditors with information needed about supplier performance, SCARs, CoC,
material specifications and receival verification process as part of preparation of an incoming audit.
Perform any assessment or action needed as a result of supplier audits. - Maintain ASL (Approved Supplier Lits in GTW) and S/4 system updated as the result of supplier
qualifications, change control actions, new material qualifications or projects activities. - Train contractors and consultants in the procedure of quality standards, requirements and GMPs
- All other duties inherent to the position and those assigned by his/her immediate supervisor, including opening or closure of actions related to deviations, NC’s, CAPAS, DCC’s, CCs, AIAs, OMR presentations and internal audit responses.
EDUCATION:
- Bachelor's degree in electrical, mechanical, electronic, electromechanical, industrial engineering, biotechnology, chemistry, computer science or related career or a combination of equivalent career experience in supplier quality rols.
- English B1
EXPERIENCE:
- 1 year of experience in regulated industries. Expertise in supplier quality management is a plus.
SKILLS:
- Knowledge on root cause determination tools, such as DMAIC or A3, among others.
- Advanced knowledge of Office applications (Windows)
- Ability to communicate written and oral ideas in a clear, concise and precise manner.
- Critical thinking and continous improvement
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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https://www.abbvie.com/join-us/reasonable-accommodations.html
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Where We Work
Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.