Randstad Material Control Clerk in Norwood, Massachusetts
Material Control Clerk
salary:$25 - $28 per hour
date posted:Tuesday, May 4, 2021
job type:Temp to Perm
Material Control Clerk
Pharmaceutical GMP Materials - Logistics & Inventory SOP Assurance
Hours: This position will be 4 days x10hour schedule with a weekend day requirement or 8 hours x 5 days over night shifts
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials. He/she will support the handling and processing of materials within manufacturing operations in accordance with established processes and procedures. The successful candidate will be able to document and communicate their operational observations clearly and efficiently. They will be curious to learn and able to demonstrate a high degree of working flexibly.
Working hours: 7:00 AM - 11:00 PM
--Safely transport product, equipment and materials (buffers, drug substance) from the warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements in support of the manufacture of mRNA medicines
--Assist manufacturing, QA and logistics colleagues in other activities as required
--Strict adherence to current good manufacturing practices, standard operating procedures, and manufacturing documentation. Establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions, and of process data.
--Receiving goods and materials through ERP management system, inspect and prioritize distribution of goods, materials, supplies and/or products ensuring accurate quantities and completing records.
--Handling material ensuring compliance throughout CNC space
--Transport materials, supplies and/or products. Transfers materials to and from Logistics and Manufacturing. Ensure accurate quantities are delivered.
--Inventory Control: document all transactions/movements and perform physical inventory checks/reconciliations.
--Other responsibilities include: proper storage, verification for accuracy, wipe down, maintaining required logs, records, security and safety.
AS Degree and/or BioWork Certification preferred; High school diploma or GED required
Experience in a highly-regulated industry, Pharmaceutical, medical device or cGMP related field
At least 1-year regulated manufacturing or material handling a plus
At least 1-5 years experience with SAP/ Oracle a plus
Maintain Cleanroom/Gown Certification
GMP experience is a plus. Good documentation practices are important.
Ability to collaborate fluidly with peers, supervisors and cross functional support groups required
Good organizational skills required
Ability to lift and move products
Proficient use of Microsoft Office (Microsoft Word and Excel).
Ability to work overtime when required
Collaborative, customer focused attitude
Apply today! Send your updated resume to email@example.com
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