Job Summary
We are seeking a highly motivated and detail‑oriented AIQ Engineer to join our Quality Control team. The AIQ Engineer will play a crucial role in ensuring reliability and compliance of Laboratory Systems. This is a full‑time on‑site role.
Responsibilities
Work with ELM team colleagues to deliver IT elements of Laboratory capital projects.
Author, review and approve documents for lab systems.
Work with site teams on generation of requirements and/or configuration of specifications and IOQ test protocols.
Involvement in risk assessments.
Support system content deployment and end‑user training.
Recognise the importance of the quality control function in pharmaceutical production; AIQ Engineer should display a high level of integrity in the performance of his/her work.
Qualifications
Experience in the support of IT applications is required.
Knowledge of 21CFR Part 11 requirements and data integrity guidelines is desirable.
Experience supporting QC laboratory systems is preferred but not essential.
Strong knowledge of Microsoft Windows Operating Systems (Windows 10/11 and server based Operating Systems).
Strong problem‑solving skills.
Strong oral and written communication skills with proven ability to communicate and build relationships cross‑functionally.
Excellent organizational and prioritization skills.
Excellent communication and interpersonal skills are essential.
Self‑motivated, detail‑oriented and possessing excellent organizational and time‑management skills.
Ability to work well both independently and in a team environment.
Ability and flexibility to perform all other job‑related and ad‑hoc duties as required.
Experience in the pharmaceutical industry is an advantage.
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