- Location
- Thousand Oaks, CA
- Workplace
- Remote
- Type
- Contract
- Department
- IT
- Seniority
- Entry
- Source
- CATS
Description
Job Title: Quality Assurance Associate, Biopharma (JP9947)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Plant Quality Assurance Incoming and Packaging
Duration: 3 years with possible conversion to FTE
Posting Date: 03/15/2022
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
Preferred qualifications:
Experience with GMP processes and documentation. Without that fundamental skillset the training for document review tasks, label approval and packaging inspection will have no foundation. Must be able to methodically and meticulously inspect printed materials for print quality defects, clinical product components (e.g. syringes and vials) for physical defects, and batch record documentation for accuracy and completeness. Must be able to work in a team with shifting priorities and shifting responsibilities, such that the team members must be confident verbal communicators able to discuss responsibilities, divide them, reassess them, and potentially reassign them throughout the day or week.
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:
Phone screen
Virtual 1:1 (45 minutes- 60) with panel
We invite qualified candidates to send your resume to [email protected]. 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: Plant Quality Assurance Incoming and Packaging
Duration: 3 years with possible conversion to FTE
Posting Date: 03/15/2022
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
Preferred qualifications:
Experience with GMP processes and documentation. Without that fundamental skillset the training for document review tasks, label approval and packaging inspection will have no foundation. Must be able to methodically and meticulously inspect printed materials for print quality defects, clinical product components (e.g. syringes and vials) for physical defects, and batch record documentation for accuracy and completeness. Must be able to work in a team with shifting priorities and shifting responsibilities, such that the team members must be confident verbal communicators able to discuss responsibilities, divide them, reassess them, and potentially reassign them throughout the day or week.
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:
Phone screen
Virtual 1:1 (45 minutes- 60) with panel
We invite qualified candidates to send your resume to [email protected]. 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.
Skills
GMP
