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QA Incoming Inspection and Material Disposition Associate

2 months ago

Devens, United States Actalent Full time

Great opportunity to get your foot in the door with one of the top Cell Therapy companies in the Devens, MA area

If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com

Description

QA Specialist Incoming Material Disposition

Onsite role Devens site

Work Schedule: Monday - Friday Business Hours

PURPOSE AND SCOPE OF POSITION

The Quality Assurance Incoming Material Disposition Specialist is responsible for supporting the incoming inspection and disposition of incoming materials such as consumables and raw materials at the Cell Therapy Facility. Perform incoming inspection and review of the disposition deliverables to support disposition of materials and batches within the inventory management systems. Assure materials comply with all company policies standards Network Global Standard Operating Procedures.

REQUIRED COMPETENCIES: Knowledge Skills and Abilities

  • Experience in a laboratory manufacturing quality or warehouse environment desired.

  • Prior evidence of successful participation on work/study teams where combined contribution collaboration and time bound results are expected.

  • Demonstrated proficiency in common computer tools such as word processing spreadsheet and web-based applications as well as ERP solutions such as SAP.

  • Previous work/academic experience where attention to detail and personal accountability were critical to success.

  • Strong communication skills and the ability to follow written and verbal instructions.

DUTIES AND RESPONSIBILITIES

  • Works closely with Supply Chain and Manufacturing with regards to discrepancy with nonconforming material as well as the incoming material process.

  • Inspects incoming materials such as consumables packaging and raw materials per Standard Operating Procedures and material specifications.

  • Performs review of the disposition deliverables to support disposition of materials and batches within the inventory management systems.

  • Assures materials comply with all company policies standards Network Global Standard Procedures.

  • Reviews documentation to support disposition of incoming materials.

  • Works in electronic systems such as SAP Learning Management and Document management systems.

  • May contribute to drafting reviewing or approving procedural documents.

  • Works on assignments of simple to moderate complexity where some judgment is required in resolving problems and making routine recommendations.

  • Other duties as required.

EDUCATION AND EXPERIENCE

  • B.S. in science engineering biochemistry related discipline or its equivalent

  • 1-2 years of directly relevant experience in a regulated cGMP environment.

  • Any combination of education experience and military service in line with recommendations above will be considered.

WORKING CONDITIONS:

  • Work is generally performed seated in a Warehouse condition but may require standing and walking for up to 10 of the time. Lighting and temperature are adequate and there are no abnormal conditions caused by noise dust etc.

  • Work in a cGMP laboratory and/or manufacturing environment following techniques which require one to maintain a high attention to detail. Properly use Personal Protective Equipment PPE gowning for restricted areas aseptic processing handling chemicals and work in a general office environment.

Experience Level

Intermediate Level

About Actalent

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  • Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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