Manufacturing Visual Inspection Technician
This role will require shift work.
Responsibilities
Document all activities in line with cGMP requirements.
Perform final product visual inspection.
Perform product intermediary packaging, as applicable.
Perform process testing methods.
Monitor Process Alarms.
Transfer final materials to warehouse inventory.
Ensure all manufacturing documentation is completed in a timely manner without errors, following cGMP's.
Diagnose and resolve events or exceptions of VI process.
Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulation, following the procedures and policies of the plant, division, and the corporation.
Keep detailed records, manual or electronic, of the operations carried out during the work shift.
Testing and commissioning and qualification of equipment.
Adhering to all relevant policies relating to Quality & Safety.
Ensure successful external inspections, and Division and Corporate audits.
Active participant in the development of batch records and electronic batch records for the site.
Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures.
Qualifications
3rd level qualification in a relevant Science discipline OR 2 years of experience in a GMP Environment.
Previous experience in a GMP environment (Pharma preferably).
Flexibility, great concentration & attention to detail.
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,
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
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