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Quality Associate

Malvern, PA

Posted: 02/18/2021 Industry: R&D Scientist Job Number: JN -022021-12546

Job Description

QUALITY ASSOCIATE

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: QUALITY ASSOCIATE
  • Location: Malvern, PA
  • Industry: Pharmaceutical
  • Hours: 1st shift Mon-Fri 8am - 5pm
  • Salary: $31hr (Paid Weekly - Benefits Available)
  • Employment Type: Long Term Contract
Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Job Scope:

The Quality job function within is responsible for ensuring all the products and services offered by
Catalent:
are of the highest quality in terms of satisfaction, predictability, and sustainability.
comply with the appropriate local regulations and laws.

Essential Functions:
Management of Batch Manufacturing Record Issuance and Reconciliation
Provide Clients/Regulatory Agencies Copies of Batch Manufacturing Records and other documents, as required
Review, approval and release of controlled supplies and packaging materials
Review, approval and release of materials for micronization
Batch Manufacturing Record Review/Approval and Product Release
Mill and Equipment Release
Secondary Responsibilities
Maintaining QA Databases
Copying/Scanning/Filing Documents
Document Development Issuing Reconciling Laboratory/Operations Worksheets/Log Sheets
Assisting with internal, external and client audits with Lead Auditor
Assist with continuous improvement projects and team objectives, as directed

Position Requirements:
Bachelor of Science in a scientific discipline or a High School Degree with 2+ years of Quality Assurance experience in a GMP manufacturing environment.
Six Sigma or ASQ certification preferred
Minimum Experience Required: 1+ years of experience in a GMP manufacturing environment

Knowledge/Skills Requirements:
Analytical Thinking Effective Communication oral & written
Attention to Detail Planning and Prioritization
cGMP Quality Principles & Concepts
Continuous Improvement Excellent Time Management Skills
Computer Skills (MS Office, Trackwise, Excel) Ability to Be a self-starter and multi-task oriented

EOE/ADA



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