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Materials Control Associate II

Harmans, MD

Posted: 12/10/2020 Industry: Manufacturing Technician Job Number: JN -122020-12275

Job Description

Materials Control Associate II

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: Materials Control Associate II
  • Location: Harmans, MD
  • Industry: Pharmaceutical
  • Hours: Mon-Fri 8AM - 5PM
  • Salary: $20.00hr (Paid Weekly - Benefits Available)
  • Employment Type: 12 month 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:

This role is responsible for supporting the overall GMP materials control/warehousing operations for a Phase II/III GMP biopharma manufacturing facility. The position requires practical experience and knowledge of a variety of activities such as materials receipt/quarantine/release, logistical support in a manufacturing facility, electronic inventory control and distribution/shipping of products

Knowledge/Skills Requirements:
Conducts reviews of GMP documentation associated with materials control (material specifications, receipt inspection forms, inventory records, item request form)
Assessing the Materials Control operation on a continuing basis and providing recommendations for improvement is encouraged
Generation of GMP documentation (SOPs, etc.) is expected
Will participate in the receipt of all GMP materials rectify discrepancies, matching vendors documentation against Company requirements (GMP and accounting).
Will distribute materials for GMP operations following approved procedures. This includes assisting in the reconciliation of all GMP materials after client campaigns
Compile and maintain inventory records
Takes receipt and inventory control of Company generated material (cell banks, bulk protein, etc.)
Assists with performing internal audits
Will participate in regulatory (FDA, EMEA) and client audits/inspections of Company and the facility
Works under general supervision to meet project goals
Works closely with QA to quarantine and release all GMP materials in a timely manner
Participation in the organization and cleanliness of the warehouse will be critical
Assists in the training of junior personnel
Will work closely with various departments at the Company and aid as needed. This may include support for pre-clinical projects
Working closely with various departments and aids as needed

SKILLS & TECHNICAL EXPERTISE:
Experience with Good Manufacturing Practices (GMPs) a plus
High School Diploma with at least 2 years of relevant experience with warehousing operations
Experience with electronic inventory control systems as well as MS Outlook and Excel
Documented training (certification) of hazardous materials
Mature professional capable of independent work
Ability to lift and carry up to 40 lbs. is required

EOE/ADA


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