Materials Control Coordinator I - Contract - Bristol, PA
Join a trailblazing biotech on the cutting edge of science and technology.
À±½·ÊÓƵ is seeking a Materials Control Coordinator I for a contract role in Bristol, PA. In this position, you will play a key role in managing inventory, shipping, purchasing, and receiving operations within a GMP environment.
Primary Responsibilities:
The successful candidate will be involved in ensuring materials are properly allocated, tracked, and maintained to support R&D lab activities, manufacturing processes, and quality control operations.
Skills & Requirements:
- High school diploma or equivalent.
- Experience in materials control coordination; familiarity with Quality Assurance environments is a plus.
- Ability to read and understand test plans, SOPs, and documentation in English.
- Strong communication skills across manufacturing and testing teams.
- Knowledge of standard practices in manufacturing and biologics environments.
- Proficiency in Microsoft Office applications.
The Materials Control Coordinator I's responsibilities will be:
- Maintain inventory for raw materials used in R&D and GMP manufacturing.
- Pull and issue materials for specific projects, including staging and un-staging for GMP processes.
- Monitor, review, and report on physical inventory levels and capacity requirements.
- Collaborate with Quality Control to ensure inspection and testing of incoming materials.
- Verify materials against internal specifications and release requirements.
- Check received materials against purchase orders and report any damaged or defective items.
- Accurately maintain records of received materials and update chemical/solvent inventory systems.
- Reconcile inventory variances with technical operations teams.
- Follow established procedures for receiving, inspection, inventory management, material transfer, and shipping.
- Oversee shipping and receiving duties and assist in maintaining the warehouse's physical condition.
- Operate ERP systems to track inventory usage and requirements.
- Communicate effectively with clients, supervisors, and colleagues.
- Adhere to quality standards, ethical practices, and company policies.
- Participate in safety initiatives, such as the Spill Team and Safety Committee.
- Perform other duties as assigned.
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
À±½·ÊÓƵ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓƵ is acting as an Employment Agency in relation to this vacancy.
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