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 I’s 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 – 318 -6506 | (W) # 732-549-2030 – Ext – 324 | (F) 732-549-5549
Email id – seema @irionline.com| www.irionline.com
LinkedIn: https://in.linkedin.com/in/seemachawhan
Gold Seal JCAHO Certified ™ for Health Care Staffing
“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES
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 I’s 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.
Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. ITLife Sciences Allied Healthcare CRO Certified MBE|GSA - Schedule 66IGSA - Schedule 621I DIRECT # - 732 – 318 -6506 | (W) # 732-549-2030 – Ext – 324 | (F) 732-549-5549 Email id–seema @irionline.com|www.irionline.com LinkedIn:https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™for Health Care Staffing “INC5000’sFASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
