3 Key Consulting is hiring a Quality Assurance Senior Associate for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
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.
Top Must have Skill Sets:
batch record approvals
visual inspection of final product
Employee Value Proposition:
At main headquarters wide areas to grow in
Interview Process: Phone screen followed by video WebEx interview
We invite qualified candidates to send your resume to firstname.lastname@example.org. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.