Job Title: Quality Assurance Senior Associate, GMP Deviation - Remote (JP9587) Location: West Greenwich, RI. 02817 (100% Remote) Employment Type: Contract Business Unit: ARI QC Lab Assurance, Systems and Technical Services Duration: 1+ years (with likely extensions and/or conversion to permanent) Rate: $33-36/Hr W2 Posting Date: 1/3/20222
3 Key Consulting is hiring a Quality Assurance Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Quality oversight of Quality Control laboratories activities equipment, systems and process with alignment into the client Quality Systems.
Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations.
Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA)
Why is the Position Open? Backfill.
Top Must Have Skills:
Track wise System
Experience with working in manufacturing or quality lab setting in the past 3+ years.
Day to Day Responsibilities: Quality oversight to QC Labs, deviation write up and closure, CAPA support.
Basic Qualifications: Quality assurance or quality control laboratory testing experience in the pharmaceutical or medical device industry
Lack of lab experience
Large gaps of employment
Video Skype Panel Interview.
We invite qualified candidates to send your resume to email@example.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.