Inspect verify and release all incoming materials in accordance with companyestablished procedures specifications and requirements. Process the commissioning of new equipment and systems. Conduct validation studies for equipment computerized systems and products ensuring compliance with company standards and medical industry regulations.
Support the implementation of improvements in the area.
MAJOR RESPONSIBILITIES
- Perform inspections and release of all incoming materials in accordance with established procedures specifications and company the inspection records from Technician I and II. Perform transactions in the ERP system as required and route the material for storage.
- Train personnel on the proper use of equipment and systems provide technical guidance and mentorship to Quality Technician I and II personnel.
- Execute and create first article inspection and other material validation activities.
- Maintain and oversee the commissioning of new equipment and direct communication with equipment suppliers for inquiries training failures and other related matters.
- Conduct validation studies for equipment computerized systems and products ensuring compliance with company standards and medical industry equipment and computerized systems in the Incoming area to ensure they remain in a validated state.
- Participate in continuous improvement initiatives to enhance inspection processes and efficiency.
- Escalate nonconforming material to the Supplier Quality Engineer and assist the Quality Technician III for system record creation.
- Support the audit process before (readiness) during (audit) and after (CAPA compliance and commitment).
- Ensure compliance with established procedures for equipment and identify necessary changes for improvement and documentation updates.
- Perform other duties as assigned by the immediate supervisor such as handling deviations nonconformances (NCs) CAPAs document control changes (DCCs) change control boards (CCBs) and document audits.
- Work overtime including weekends and holidays when required by business needs.
Qualifications :
- Quality Technician or Electromecanical Technician
- 80 Industrial Engineering/Chemical Enginering/Electromechanical Engineering Student or other related field to incoming inspection (Desirable)
- 3 years in quality inspector or related field in ISO compliance company.
- Electromechanical component inspection.
- Experience in hazardous waste and hazardous substances handling.
- Knowledge of proper ergonomic positions for lifting and material handling.
- Root CauseDMAICA3 tools (Desirable)
- MS office aplications/SAP
- Ability to read and interpret engineering drawings and technical specifications. Basics of GD&T
- Proficiency in using measuring instruments (calipers micrometers optic comparator etc..
- A2 English
- Basic knowledge of statistical process control (SPC)
- Attention to details/Continuos improvement
- Driving License (Desirable)
Additional Information :
We offer:
- Chance to become a part of dynamically growing biopharmaceutical company.
- Friendly organizational culture
- Training opportunities and professional development.
- Flexible working hours and additional days off (Abbvie Days).
- Charity initiatives incl. Week of possibilities days of employee volunteering.
- Extensive benefits package (Multisport private medical care life insurance).
- Wellness initiatives global events promoting worklife balance physical and mental wellbeing
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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Work :
No
Employment Type :
Fulltime