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Commonwealth Sciences

Contract Logistics Specialist II (GMP)

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What they do

A Contracts Analyst reviews business contracts for a company or organization. Reviews proposed contract terms and conditions, communicates with management about contract obligations, and communicates and negotiates with clients. Prepares contract cost estimates and reviews proposals for contract changes. Confirms that contract terms have been met before a contract is closed out.

$79,381 / year median in Massachusetts

-3% projected decline

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Job Description

Contract Logistics Specialist II (GMP) Commonwealth Sciences - 4.5 Waltham, MA Job Details Contract 14 hours ago Qualifications High school diploma or GED Cross-functional collaboration Cross-functional communication
Full Job Description Job ID:
#10558 Contract Logistics Specialist II (GMP) Waltham, MA Science GMP Manufacturing Position located in
Waltham, MA Responsibilities:
Coordinate day-to-day material movement activities, including receiving, shipping, storage, and internal distribution. Process incoming deliveries, inspecting shipments for quantity, condition, and potential damage. Review purchase orders, packing lists, and related documentation to ensure received materials match established requirements. Assist with inventory control through routine cycle counts, inventory reconciliations, and stock verification. Properly identify, label, store, and distribute materials according to established procedures and operational requirements. Keep warehouse and storage areas orderly, clean, and maintained in a state of readiness for internal and external inspections. Work closely with Operations and Quality Assurance to verify that incoming materials are appropriately reviewed and released for use. Complete additional material management and departmental activities as needed.
Requirements:
High School diploma, GED, or equivalent required. 1-3 years of experience in warehouse operations, materials management, shipping/receiving, or inventory control; experience in a cGMP, pharmaceutical, biotech, medical device, or other regulated setting is preferred. Strong attention to detail with effective written and verbal communication skills. Ability to prioritize tasks, work independently, and collaborate effectively with cross-functional teams. Familiarity with cGMP material handling and storage practices, including the segregation and control of Quarantine, Released, and Rejected materials, preferred. IND1