3key Consulting, Inc.
Quality Assurance Associate, Biopharma (JP9947)
3key Consulting, Inc., Thousand Oaks, California, United States, 91362
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 client, a leading global biopharmaceutical company.
Job Description: Primary responsibilities include inspecting raw materials, components, and labels; sampling raw materials, labels, and utilities; generating and compiling quality data and reports (e.g., lot track/trace, incidents). The role also involves assisting with document review, initiating incidents, and overseeing room clearance inspections.
Skills & Qualifications:
Experience in quality assurance or manufacturing within the pharmaceutical or medical device industry.
Experience with GMP processes and documentation.
Ability to methodically 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.
Strong teamwork skills with the ability to adapt to shifting priorities and responsibilities, and communicate effectively.
Bachelor’s degree is preferred but not required.
Day-to-Day Responsibilities: Perform incoming inspection of raw materials, ensuring quality standards are met.
Employee Value Proposition: Opportunity for career growth and development.
Red Flags:
Candidate cannot be color blind.
Lack of willingness to learn; candidate should be proactive and motivated.
Interview Process: Phone screening followed by a virtual 1:1 interview with a panel (45-60 minutes).
Qualified candidates are invited to send their resume to
recruiting@3keyconsulting.com . For other opportunities, visit our website at
www.3keyconsulting.com/careers . Feel free to share this opportunity with interested contacts.
#J-18808-Ljbffr
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 client, a leading global biopharmaceutical company.
Job Description: Primary responsibilities include inspecting raw materials, components, and labels; sampling raw materials, labels, and utilities; generating and compiling quality data and reports (e.g., lot track/trace, incidents). The role also involves assisting with document review, initiating incidents, and overseeing room clearance inspections.
Skills & Qualifications:
Experience in quality assurance or manufacturing within the pharmaceutical or medical device industry.
Experience with GMP processes and documentation.
Ability to methodically 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.
Strong teamwork skills with the ability to adapt to shifting priorities and responsibilities, and communicate effectively.
Bachelor’s degree is preferred but not required.
Day-to-Day Responsibilities: Perform incoming inspection of raw materials, ensuring quality standards are met.
Employee Value Proposition: Opportunity for career growth and development.
Red Flags:
Candidate cannot be color blind.
Lack of willingness to learn; candidate should be proactive and motivated.
Interview Process: Phone screening followed by a virtual 1:1 interview with a panel (45-60 minutes).
Qualified candidates are invited to send their resume to
recruiting@3keyconsulting.com . For other opportunities, visit our website at
www.3keyconsulting.com/careers . Feel free to share this opportunity with interested contacts.
#J-18808-Ljbffr