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Quality Specialist – GMP Manufacturing & Compliance

Freyr Solutions, Client: Global Pharma company
West Point, PA Full Time
POSTED ON 3/6/2025
AVAILABLE BEFORE 5/29/2025

Freyr is hiring for a leading pharmaceutical client!!

You could be just the right applicant for this job Read all associated information and make sure to apply.

Job Title : Quality Specialist

Location : West Point, PA 19486

Duration : Long term contract

Qualifications : Required Education :

  • Bachelor's degree, in a scientific or engineering field (preferred); candidates with degrees in other fields will be considered if accompanied by significant relevant experience.

Required Experience and Skills :

  • Minimum 1-2 years of relevant post-degree work experience in GMP Manufacturing or Laboratory environment, Pharmaceutical / Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing or laboratory operations, or related industry experience in a laboratory, manufacturing, science related or regulated setting.
  • Familiarity with GMP documentation review
  • Understanding of cGMPs and of regulatory requirements as they apply to the pharmaceutical field or a related area..
  • Responsibilities :

    The Quality Specialist provides direct Quality support to a production area as part of a Quality IPT (Integrated Product Team). With guidance from the Batch Record Review Quality Manager, the Quality Specialist ensures quality, and compliance of products manufactured by the functional area and adherence to Good Manufacturing and Documentation Practices.

    Primary Activities :

  • Fully trained in relevant Standard Operating Procedures (SOPs), Work Instructions (WIs) and competency-based activities
  • Learns cGMPs, the manufacturing process, and our company quality systems, including SAP, GLIMS and electronic logbook, laboratory data, and batch record platforms
  • Provides presence on the shop floor to support compliance and data integrity.
  • Reviews production documentation such as batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures and ensures completion of proper remediation of errors
  • Reviews and approves new and updated SOPs and Controlled Job Aids
  • Actively participates in the Tier process and uses this forum to make concerns visible and to partner with the functional area on resolution
  • Fosters a customer service attitude within the functional area
  • For more details and prompt consideration, please share your resume and we can schedule a call to discuss further.

    Regards,

    Praveen B

    Team Lead, Staffing Dept

    Phone : 609-681-2417

    praveen.bodike@freyrsolutions.com

    www.freyrsolutions.com

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