Incoming Quality Control Technician - Operations
AstraZenecaUs - west chester - ohUpdate time: January 11,2020
Job Description

At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe.

Description:

The Incoming Quality Control Technician autonomously performs tasks related to inspection and sampling to support the release of production materials and components.

  • Performs testing of samples. Maintains and troubleshoots testing equipment.

Essential Job Functions:

  • Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts from technical documentation.
  • Maintain accurate and complete records (for example: laboratory notebooks, quality records, sample receipts).
  • Complete required training.
  • Ensure that weights, measures, and raw materials are managed appropriately so that manufactured batches contain proper ingredients and quantities.
  • Perform visual inspections.
  • Verify count, measure and check materials to ensure proper components, quantities, and/or characteristics.
  • Use MAXIMO and/or CMMS (Computerized Maintenance Management System) to manage logistics. Use SAP to track inventory and materials.
  • Guide others on SOPs (Standard Operating Procedures), control documents, and/or other work instructions. Coordinate activities of support groups.
  • Identify temporary and permanent fixes to address issues.
  • Monitor records to ensure compliance with regulatory requirements.
  • Create, generate, type, proof, and distribute correspondences.
  • Ensure that incoming materials are inspected and released.
  • Ensure that others carry out laboratory duties in a manner consistent with cGMP.
  • Interpret quality standards to ensure all incoming materials comply with requirements.
  • Perform regular audits of SOPs (Standard Operating Procedures) and/or work instructions.
  • Perform routine sampling activities and associated data entry.
  • Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities.
  • Read and interpret diagrams, drawings, and other schematics.
  • Recommend and initiate activities to ensure area and equipment is maintained in a state of compliance.
  • Provide 24/7 "on-call" support to others.
  • Provide feedback on service and quality issues on a timely basis.
  • Provide general office support (for example: directing calls, filing, photocopying, etc.)

Minimum Requirements:

  • High school diploma or GED required
  • 1 Year of experience in a pharmaceutical or regulated environment
  • Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language.
  • Good attention to detail is required. Individual must be capable of keeping accurate records and performing mathematical calculations.

Preferred Background:

  • 2 years of experience in a pharmaceutical environment supporting incoming quality.

Next Steps – Apply today!

 

To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience – it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity.  If you know someone who would be a great fit, please share this posting with them.

Date Posted

10-Jan-2020

Closing Date

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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