Sr. Site Quality Authority (SQA), Investigations & Compliance
United States - Kansas - McPhersononsitesenior$99K – $165K
Posted yesterday · via Workday
About this role
ROLE SUMMARY The Sr. Site Quality Authority (SQA), Investigations & Compliance role provides is responsible for overseeing GMP manufacturing investigations, including review and approval of investigations, interim reports, commitments, and complex deviation records. In addition, to any other GMP documentation such as validation & qualification reports, procedures. The candidate will be responsible for performing thorough, detailed, and timely investigation reviews and approvals.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
For this role: teams
2
Level fit
This role is senior-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in United States - Kansas - McPherson. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
Pulled from the job description. These are the keywords we'll weight when scoring your fit.
teams
More at Pfizer
- View →医学信息沟通专员CHN - JS - Jiangsu
- View →Operational Excellence Project ManagerRomania - Bucharest
- View →医学信息沟通地区经理-II&GE-北京China - Beijing - Beijing
- View →Key Account Manager, Private and Government Hospitals, MindanaoPhilippines - Makati City
- View →Director, Operational ExcellenceUnited States - New York - New York City
- View →Sr. Manager, Solution Engineer, Visualization, Analytics & CollaborationUnited States - New York - New York City
