Job Description

About Torbay Pharmaceuticals

At TP we have our own special kind of chemistry. Our heritage spans over 50 years with a track record of manufacturing essential medicines across the UK and beyond. With backing from an investment partner are now forging a new path in the private sector.


We are a growing and ambitious business and with this comes opportunities for our people. At TP, we are going places. A career with us means a career helping save lives. We bring skills of all levels and experiences together; not all of our people begin their working lives in pharma. Together we can make lives better.

Position:

-------------

About the Role

We're looking for a technically skilled and compliance focused

QC Equipment Specialist

to lead the introduction, validation, and lifecycle management of laboratory instruments and computerised systems. This is a pivotal role in our Quality Control team -- ensuring our equipment meets the highest regulatory standards (MHRA, FDA) and supports data integrity from day one.


You'll work closely with internal teams and external vendors to deliver projects that are technically sound, fully compliant, and future-ready.

What you can expect in a

QC Equipment Specialist

role at TP:

Deliver on the QC equipment strategy. Lead in the validation of new and replacement QC equipment, following our internal change control process. Define the user requirement (URS) for each project and ensuring it is aligned with all relevant regulatory and safety guidance. Facilitate technical and compliance discussions with internal stakeholders & suppliers. Lead the development and execution of IQ/OQ/PQ protocols for instruments and CSV protocols of computerised systems. Ensure systems support data integrity, audit trails, electronic signatures, and secure access controls. Act as the primary liaison with new equipment and software vendors. Define the equipment service & calibration schedules. Initial set up of contracts, warranties, and maintenance agreements. Support the administration and ongoing development of the Laboratory Information Management System (LIMS).

Requirements:

-----------------

What are we looking for:

Familiarity with analytical instruments such as HPLC, GC, UV-Vis, FT-IR, and ICP. This should include the scientific principles behind the techniques, typical instrument functionality and process flow in a regulated QC environment. Strong computer literacy, including experience with laboratory informatics systems (e.g. CDS, LIMS). Ability to interpret regulatory guidance, technical specifications, equipment manuals and 3 party validation protocols. Strong understanding of general GxP principles (FDA, MHRA) The ability to combine the analytical, technical, regulatory and compliance elements into relevant and clear technical documents. Able to manage multiple: projects, documents, timelines, and reviews. Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field. Relevant experience in a regulated laboratory environment, preferably in the pharmaceutical industry. Experience with laboratory informatics systems. Excellent communication, documentation, and project management skills.

What we offer in return

At the heart of Torbay, we offer roles and career opportunities on your doorstep that you won't find elsewhere. With defined career pathways, and the chance to move between roles and different departments, we support your career journey at every stage. TP is going places. International expansion means growth and new opportunities.


Our benefits set us apart. With 27 days holiday as standard, group life assurance, pension and more - we reward our people for getting the job done.