Senior GMP Material Coordinator
Tewksbury, MA 
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Posted 30 days ago
Job Description
Description

As the leading company in a niche scientific market, CIL works with cutting edge researchers in clinical diagnostics, metabolic research, proteomics, environmental testing, protein discovery, drug development, metabolomics, and industrial research. CIL's growing customer base spans academia, pharmaceutical and industry, enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

Cambridge Isotope Laboratories, Inc. is seeking a Senior GMP Material Coordinator based onsite in our Tewksbury, MA location. The Senior GMP Material Coordinator will be working under general supervision, perform GMP related functions and daily activities of Supply Chain and Inventory management.

Responsibilities

  • Perform QC submission of GMP products/systems/processing aids
  • Responsible for the inventory management processes and work on improving the inventory accuracy to reduce/eliminate inventory disruption in the supply chain
  • Ensure the right level of safety stock for all critical/noncritical material to limit disruptions to our processes/production schedule
  • Perform inventory count of GMP raw materials/processing aids/finished products and reconciliation to ensure accuracy in inventory management
  • Perform quarterly reviews of controlled logbooks
  • Attend biweekly production meeting with stakeholders
  • Collaborate and coordinate interfacility transfer of materials with Andover, MA & Xenia, OH locations
  • Provide support for all GMP duties in both location including, but not limited to, receiving GMP incoming goods/raw materials, performing weekly GMP raw material inventory check, and stock, rotate and segregate GMP materials, bulk, and packaged product
  • Provide support for Packaging department with weighing and/or packaging of finished products
  • Perform all GMP related Quality functions - Deviation, Risk assessment, CAPAs
  • Perform any additional tasks as necessary
  • Issuance of GMP controlled documents/batch records for operations
  • Review/reconcile all dispensing forms (raw materials, bulk and finished) upon completion. Investigate discrepancies prior to submission to QA
  • Coordinate disposals/transfer of expired materials
Requirements
  • High School Diploma
  • Minimum of 2 years' experience working within a warehouse or product handling environment
  • GMP/GDP experience preferred
  • Must have a strong work ethic, be flexible to changing work demands and an effective team player
  • Must have a strong understanding of GMP concepts and procedures
Benefits

CIL offers a competitive salary and a comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.

CIL is an EEO/Affirmative Action employer.

Learn more about us on our website:


About us:

As the leading company in a rapidly expanding increasingly critical scientific market, CIL and our subsidiaries supply over 15,000 products to 30,000 research customers around the world and work with cutting edge researchers in clinical diagnostics, metabolic research, proteomics, environmental testing, protein discovery, nuclear medicine, drug development, metabolomics, semiconductor, OLED and industrial applications. CIL has had consistent growth and profitability for over 40 years. CIL's growing customer base spans academia, pharmaceutical and industry, enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well as pioneering research groups that have expertise in product development to drive market growth.

Cambridge Isotope Laboratories, Inc., with headquarters in Tewksbury, MA, is the world's premier producer of stable isotope labeled compounds and a world leader in the field of stable isotope separations. CIL has over 675 employees with laboratories in the U.S., Canada, France and Germany. CIL is a subsidiary of the Otsuka Pharmaceutical Group.

For over 40 years, CIL has specialized in the development, production, and marketing of stable isotopes and chemical compounds labeled with stable isotopes. Join us for excellent career opportunities as we drive the expansion of market applications with innovative product development.

Learn more about us on our website:

 

Job Summary
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
High School or Equivalent
Required Experience
2+ years
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