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.
Job Description:
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:
Deviation experience
Track wise System
GMP
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
Red Flags:
Lack of lab experience
Large gaps of employment
Interview process:
Video Skype Panel Interview.
We invite qualified candidates to send your resume to resumes@3keyconsulting.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.