Technician, Incoming Laboratory IV (Temporal hasta diciembre 2025)
Technician, Incoming Laboratory IV (Temporal hasta diciembre 2025)
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Salary Not Disclosed
1 Vacancy
Job Description
Inspect verify and release all incoming materials in accordance with company-established procedures specifications and requirements. Process the commissioning of new equipment and systems. Conduct validation studies for equipment computerized systems 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 requirements. Verify the inspection records from Technician I and II. Perform
transactions set up new part numbers 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 II and III personnel.
Area SAP SME
Execute and create first article inspection and other material validation activities.
Oversee OEMs supplier communications and release/shipment coordination.
Oversee the purchase and commissioning of new equipment and systems ensuring compliance with the
laboratory budget.
Maintain and manage equipment while maintaining direct communication with suppliers for inquiries training
failures and other related matters.
Maintain software draft and execute test methods and Machine Operation (MO) procedures as well as upgrade existing ones to ensure compliance with AbbVie documentation standards.
Develop Draft and execute validation protocols for equipment computerized systems items and products
ensuring compliance with company standards and medical industry regulations. Revalidate 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 non-conforming 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 non-conformances
(NCs) CAPAs document control changes (DCCs) change control boards (CRBs) and document audits.
Work overtime including weekends and holidays when required by business needs.
Qualifications :
EDUCATION
Quality Technician or Electromecanical Technician
80% Industrial Engineering/Chemical Enginering/Electromechanical Engineering Student or other related field to incoming inspection(must)
EXPERIENCE
4 years in quality inspector Validation Technician or related field in ISO compliance company.
Electromechanical component inspection.
Experience in hazardous waste and hazardous substances handling.
Quotation purchasing equipments (Desirable)
Knowledge of proper ergonomic positions for lifting and material handling.
Root CauseDMAICA3 tools (Desirable)
SKILLS
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.).
B2 English
Basic knowledge of statistical process control (SPC)
Attention to details/Continuos improvement
Driving License (Desirable)
Additional Information :
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.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Employment Type
Full-time
