Job Description
Support pharmaceutical manufacturing operations and technical groups in owning document revision and routing, driving timely approval, and designing facility/process procedures and business processes. This role involves managing documents in line with site quality assurance programs and local standard operating procedures.
Key Responsibilities:
* Design, update, and improve facility/process procedures and business processes
* Own document revision and routing on document management systems
* Drive timely approval of documents
* Manage documents in line with site quality assurance programs and local standard operating procedures
Required Skills and Qualifications
Relevant engineering/science qualification or operational experience is required. A master's degree in engineering/science is desirable. Previous pharma production, operations/project experience is necessary, along with a strong sense of customer focus and teamwork.
* Relevant engineering/science qualification or operational experience
* Master's degree in engineering/science (desirable)
* Previous pharma production, operations/project experience
* Strong sense of customer focus and teamwork
Benefits
This role offers the opportunity to support a dynamic large molecule manufacturing environment, develop a key understanding of core manufacturing principles, and be involved in new product introductions (NPI).
* Support a dynamic large molecule manufacturing environment
* Develop/learn key understanding of core manufacturing principles
* Involved in new product introductions (NPI)
Others
This role requires a self-motivated/proactive approach with the ability to operate without close supervision, proven problem-solving skills, and a commitment to meeting deadlines.
* Self-motivated/proactive approach with the ability to operate without close supervision
* Proven problem-solving skills
* Commitment to meeting deadlines
Additional Information
Covalen champions diversity and equality, recognizing the collective strength found in diverse backgrounds, skills, and experiences.
We are an equal opportunity employer and welcome applications from all qualified candidates.