Materials Control Associate Ii

Immediate Opportunity!

Schedule: Rotating Shifts (2-2-3) 

7:00 AM – 7:00 PM

ROTATION SCHEDULE. WAREHOUSE EXP.
The Materials Control Associate II is accountable for GMP (Good Manufacturing Practices) 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 receiving/processing, logistical support in a manufacturing facility, electronic inventory control and distribution/shipping of products. Be able to train peers in functional execution.
 

KEY RESPONSIBILITIES

• Will distribute materials for GMP operations following approved procedures. This includes assisting in the reconciliation of all GMP materials after client campaigns. (primary duties)
• Proper labeling accountability assessing and adherence. (primary duties)
• Reconciling inventory discrepancies, cycle counts, investigate and troubleshoot root cause inventory deficiencies. (primary duties)
• Attention to detail. (primary duties)
• Reviews of GMP documentation associated with material control (material specifications, inbound material inspection forms, SOP’s, inventory records, item request forms etc.)
• Will take part in the receipt of all GMP materials – rectify discrepancies, matching vendors’ documentation against Catalent requirements (GMP and accounting).
• Ensure alignment with applicable procedures relating to shipment of CRT, Ambient, Cold-Chain shipments.
• Works closely with QA (Quality Assurance) to quarantine and release all GMP materials on time
• Participation in the organization and cleanliness of the warehouse will be critical
• Aids in the training of “junior” personnel
• Will work closely with various departments at Catalent and aid as needed. This may include support for pre-clinical projects
• Assessing the Materials Control operation on a continuing basis and supplying recommendations for improvement is encouraged.
• Compile and maintain inventory records
• Deviation, CAPA (Corrective Action Preventive Action) and Change Control knowledge.
• Understanding of process quality controls that support raw material integrity.
• Takes receipt and inventory control of Catalent generated material (cell banks, bulk protein, etc.)
• Aids with performing internal audits
• Works under general supervision to meet project goals.
• All other duties as assigned.

QUALIFICATIONS/REQUIREMENTS:

• Education: GED or High School Diploma required
• Experience: 2 years of general warehouse and/or Supply Chain experience
• Experience and a thorough understanding in coordination of warehousing activities with manufacturing and other departments (QA, QC) to maintain internal and project schedules.
• Will need experience in the shipping of a variety of materials requiring special conditions (temperature, hazardous).
• Ability to walk, stand, and bend for extended periods of time
• Ability to lift and carry up to 40 lbs.