Job title: Quality Control Associate
Location: Research Triangle Park, NC
Duration: 12+ months (possibility of extension)
ROLES & RESPOSNISBILTIES:
- The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Client RTP Drug Product facility.
- This includes performing incoming sampling and inspections for various raw materials for both the oral solid dose and parenteral facilities.
- The Raw Material Associate Iβs responsibilities include, but are not limited to, training, sampling/inspection support for raw materials, including active pharmaceutical ingredients, packaging components as well as excipients, while maintaining, robust and compliant cGMP documentation practices.
- Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, maintaining retention (retain) samples, and completing all training/course requirements while maintaining 100% compliance on all assignments.
- This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.
- The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.
- The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.
*Must be able to move 50 lbs with assistance of equipment.
We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.
Thanks & Regards,
Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
DIRECT # - 732 β 318 -6506 | (W) # 732-549-2030 β Ext β 324 | (F) 732-549-5549
Email id β seema @irionline.com| www.irionline.com
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