Contingent Quality Control Technician

Portsmouth, NH

Posted: 04/24/2020 Job Number: JN -062020-11674

Job Description

Quality Control Technician

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Title: Contingent Quality Control Technician
Location: Portsmouth, NH
Industry: Pharmaceutical
Shift Hours: Sunday to Wednesday, or Wednesday to Saturday. First and Second shifts available.
Salary: $25.00 Based on Experience
Employment Type: Long Term Contract (Benefits Available)

Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.

Summary
The Contingent Quality Control Technician will act as a team member of the Quality Control department to support routine environmental monitoring of air, surface, and clean utilities for manufacturing of in-process and final product drug lots for customers. Provide on-time, high quality results to meet Manufacturing demands.

Overview
  • Oversee assigned projects in group and ensure on track for on-time completion
  • Represent QC in customer meetings to receive/deliver information, request and requirements.
  • Document writing/review for transfers/validations/investigations
  • Measures throughput, performance and other appropriate metrics and report them to management
  • Other such as leading OE initiatives and improvements.
  • Perform other duties as assigned
Qualifications
  • High school Diploma or equivalent, advanced education in life science, microbiology, biology or similar preferred
  • Adherence to cGMP (Good Manufacturing Practices) is required.
  • Use of Laboratory computer systems or GMP Quality Systems
  • Perform routine monitoring and obtaining of samples
  • May assist with testing and analysis of samples
  • Working experience completing tasks or assignments within dedicated deadlines
  • Experience with Microsoft Suite Products (Outlook, Excel)
  • Ability to follow instructions and processes
  • Strong ability to communicate, both verbal and written
  • GMP and Aseptic Technique experience or training preferred
  • Displays commitment to quality and performs job functions to the best of your ability
  • Ability to work at least one weekend day
EOE/ADA
Search words: GMP, Quality Control, Aseptic
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