We have a current opportunity for a Associate Director QC (m/f/d) on a permanent basis. The position will be based in Spain.
Our client is a global pharmaceutical company expanding their activities in Spain. Therefore there are looking for a QC Associate Director to overview the team.
If your profile matches the following requirements and you are looking for new challenges, apply directly.
Activities:
* Oversees day-to-day operations of the Quality Control commercial program testing functions, including stability
* Manages laboratory personnel and oversees their selection, performance management, mentoring, and career development
* Supports laboratory investigations, change controls, and CAPAs for relevant QC operations
* Contributes to budget planning and resource allocation
* Provide testing data and other required quality-related information needed to support product studies
* Assists in development, implementation, and maintenance of general laboratory operational QC/IT systems in accordance with cGMP requirements
* Provides support to audit teams for Health authority, Internal/External and vendor audits
* Ensures teams performs tasks as needed to maintain GMP compliance
Profile:
* Minimum education required: Bachelor's Degree in a relevant scientific discipline
* Minimum experience required: 10 + years in applied industry experience; 4-6 years of management/supervisory experience
* Demonstrated proficiency with Quality System Records, Deviations, Change Controls and CAPAs
* Familiarity with QC operations including bioassay, chemistry, and microbiology
* HPLC Instrumentation/ Software experience is preferred
* Strong written and oral communication skills as well as organizational skills
* Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
* Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations.
