Key Role:
We are seeking a skilled Document Specialist to join our Pharmaceutical Manufacturing Operations team.
The successful candidate will be responsible for owning document revision and routing, designing and improving facility/process procedures and business processes, as well as creating and updating various documentation.
Responsibilities:
* Manage documents in the site documentation management system in line with the site quality assurance program and local standard operating procedures.
* Design, update, and improve manufacturing batch records, operations area logbooks, training documentation, and other related documents.
* Support multiple manufacturing functions (Eng, Chemistry, QA, EHS, Micro) and participate in New Product Introductions (NPI).
Requirements:
* A relevant engineering or science 3rd-level qualification or operational experience is required.
* A Master's degree in engineering or science is desirable.
* Previous pharma production, operations, or projects experience is essential.
* Demonstrated flexibility, problem-solving skills, and a proactive approach are necessary.
Benefits:
This role offers a dynamic work environment, opportunities for professional growth, and a chance to develop key understanding of core manufacturing principles.
As an equal opportunity employer, we value diversity and equality, promoting an inclusive environment for all team members.
About Us:
We are industry pioneers collaborating with organizations worldwide for over 25 years. Our tailored BPO solutions forge powerful partnerships, helping clients achieve their unique goals.