Job Title: Quality Assurance Senior Associate - (JP9291) Location: Thousand Oaks, CA. (100 REMOTE) Employment Type: Contract Business Unit: ATO Drug Product Quality Assurance Duration: 2 years (with likely extensions and/or conversion to permanent) Posting Date: 10/21/2021
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: This position supports client’s Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering staff in the execution of their processes, procedures, and use of quality systems. Duties include purposeful presence on the shop floor, electronic batch record creation, batch record review, SOP revision approval, work order approval, and quality approval of minor deviations and CAPA records. Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. The Sr. Associate will also represent functional area quality for the Drug Product Quality Assurance department in the execution of projects necessary to achieve departmental operational goals and will work in a team matrix environment.
Why is the Position Open? Additional workload on team
Top Must Have Skills:
Day to Day Responsibilities:
Batch record approvals.
Visual inspection of final product.
Employee Value Proposition:
At main headquarters with wide areas to grow.
Video Skype Panel Interview
We invite qualified candidates to send your resume to email@example.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.