Job Details
Duration:0-6 month(s)
Description/Comment:PAY - *** - MARKUP - 50% - ONSITE POSITION - DURATION - 6 MONTHS - SHIFT - 7AM - 7PM - 2-2-3 ROTATION SCHEDULE.
The Materials Control Associate I 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, SOPs, 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 of High School Diploma required
Experience: At least 6 months of general warehouse experience
Ability to walk, stand, and bend for extended periods of time
Ability to lift and carry up to 40 lbs.
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.