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Quality Assurance Associate, Biopharma (JP10223)
Thousand Oaks, CA · Biotech/PharmaceuticalJob Title: Quality Assurance Associate, Biopharma (JP10223)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Drug Product Quality Assurance
Duration: 3 years with possible conversion to FTE
Posting Date: 05/06/2022
3 Key Consulting is hiring a Quality Assurance Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Primary responsibilities of this position include inspecting raw materials, components, and labels, in addition to sampling raw materials, labels, and sanitary utilities, and generating/compiling quality data and reports (e.g. lot track/trace, incidents). Will also assist with document review and initiate incidents, as well as coordinate and compile general documents and oversee room clearance inspection.
Skills: quality assurance or manufacturing experience in the pharmaceutical or medical device industry
Top Must-Have Skill Sets:
Day to Day Responsibilities:
Performing incoming inspection of raw materials (incoming quality assurance for all raw materials on the campus)
Employee Value Proposition:
Career growth/ opportunity
Red Flags:
Candidate cannot be color blind - vision requirements listed above
Lack of willingness to learn - candidate needs to be a "go - getter"
Interview process:
Panel Interview
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Drug Product Quality Assurance
Duration: 3 years with possible conversion to FTE
Posting Date: 05/06/2022
3 Key Consulting is hiring a Quality Assurance Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Primary responsibilities of this position include inspecting raw materials, components, and labels, in addition to sampling raw materials, labels, and sanitary utilities, and generating/compiling quality data and reports (e.g. lot track/trace, incidents). Will also assist with document review and initiate incidents, as well as coordinate and compile general documents and oversee room clearance inspection.
Skills: quality assurance or manufacturing experience in the pharmaceutical or medical device industry
Top Must-Have Skill Sets:
- Bachelor’s degree not required but preferred
- Firm quality mindset is vital**** the job needs to be treated like everyday is their 1st day
- Highly motivated and willing to lear
- Team player
Day to Day Responsibilities:
Performing incoming inspection of raw materials (incoming quality assurance for all raw materials on the campus)
Employee Value Proposition:
Career growth/ opportunity
Red Flags:
Candidate cannot be color blind - vision requirements listed above
Lack of willingness to learn - candidate needs to be a "go - getter"
Interview process:
Panel Interview
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team