We are seeking an accomplished professional to fill a pivotal role within our Biopharmaceutical organization.
About the Role
This exciting opportunity is perfect for a driven individual who is passionate about delivering exceptional results in a dynamic environment.
The successful candidate will be responsible for designing, authoring, reviewing, and approving qualification/validation documentation and process development studies, as well as executing execution/development of change controls. They will also contribute to Kaizen events, provide technical input into quality notifications, and execute equipment/qualification validation programs.
Key Responsibilities
* Design, author, review, approve, and execute qualification/validation documentation and process development studies.
* Execute execution/development of change controls.
* Contribute to Kaizen events.
* Provide technical input into quality notifications.
* Execute equipment/qualification validation programs.
Requirements
To be considered for this position, applicants should possess a Bachelor's Degree or higher in a Science, Engineering, or Technical discipline, with a minimum of 3 years' experience in manufacturing, preferably in a GMP setting. Strong leadership skills, project management experience, and evidence of continuous professional development are highly desirable.
What We Offer
In return for your expertise, we offer a competitive compensation package, opportunities for growth and development, and a collaborative work environment that values innovation and excellence.
If you are a motivated and experienced professional looking for a new challenge, please do not hesitate to contact us for further information.