What are the responsibilities and job description for the Quality Assurance Associate, Biopharma Medical Device (JP9524) position at 3 Key Consulting?
Job Title: Quality Assurance Associate, Biopharma Medical Device (JP9524)
Location: Thousand Oaks, CA. Onsite
Employment Type: Contract
Business Unit: Plant Quality Assurance Incoming and Packaging
Duration: 2 years with possible extension or conversion to FTE
Posting Date: 12/14/2021
3 Key Consulting is hiring a Quality Assurance Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
This position will provide operational QA support of a clinical drug product packaging and labeling team. Primary responsibilities will include review and approval of printed clinical labels, finished clinical pack inspection, expiration date calculation and batch record review. Secondary responsibilities will include generation and compilation of quality data and reports (e.g. lot track/trace, deviations). Individual will also assist with procedure reviews and initiation of deviation reports. There is the potential for role expansion into support of a product distribution function.
Skills: quality assurance or manufacturing experience in the pharmaceutical or medical device industry
Must have 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:
Primary responsibilities will include review and approval of printed clinical labels, finished clinical pack inspection, expiration date calculation and batch record review. Secondary responsibilities will include generation and compilation of quality data and reports (e.g. lot track/trace, deviations). Individual will also assist with procedure reviews and initiation of deviation reports. There is also the potential for role expansion into support of a product distribution function.
Employee Value Proposition:
Good team atmosphere and supportive team
Opportunity to learn and grow
Red Flags:
* Jumping from position to position
* Lack of attention of details
* A minimum of 1 year of experience in Quality Assurance
Interview process:
Phone screen
Virtual 1:1 (45 minutes- 60) with panel
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to take a 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. Onsite
Employment Type: Contract
Business Unit: Plant Quality Assurance Incoming and Packaging
Duration: 2 years with possible extension or conversion to FTE
Posting Date: 12/14/2021
3 Key Consulting is hiring a Quality Assurance Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
This position will provide operational QA support of a clinical drug product packaging and labeling team. Primary responsibilities will include review and approval of printed clinical labels, finished clinical pack inspection, expiration date calculation and batch record review. Secondary responsibilities will include generation and compilation of quality data and reports (e.g. lot track/trace, deviations). Individual will also assist with procedure reviews and initiation of deviation reports. There is the potential for role expansion into support of a product distribution function.
Skills: quality assurance or manufacturing experience in the pharmaceutical or medical device industry
Must have 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:
- 1 GMP processes and documentation experience
- Good Manufacturing practices
- Inspection and QA background.
- Attention to detail; assign expiration dates on labels, providing info on labels, and documentation
- Packaging experience, is preferred
Day to Day Responsibilities:
Primary responsibilities will include review and approval of printed clinical labels, finished clinical pack inspection, expiration date calculation and batch record review. Secondary responsibilities will include generation and compilation of quality data and reports (e.g. lot track/trace, deviations). Individual will also assist with procedure reviews and initiation of deviation reports. There is also the potential for role expansion into support of a product distribution function.
Employee Value Proposition:
Good team atmosphere and supportive team
Opportunity to learn and grow
Red Flags:
* Jumping from position to position
* Lack of attention of details
* A minimum of 1 year of experience in Quality Assurance
Interview process:
Phone screen
Virtual 1:1 (45 minutes- 60) with panel
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to take a 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.