Manufacturing Technical Specialist (1 Year Contract)

Overview

Our client is a leading biopharmaceutical manufacturing organisation with a strong commitment to quality, operational excellence and patient safety. They are seeking a Manufacturing Technical Specialist on a contract basis to support manufacturing operations across campaign readiness, execution and product release.

Role

You will support Manufacturing Operations throughout the full campaign lifecycle, ensuring activities are appropriately planned, documented and executed in accordance with GMP requirements. This includes preparing and revising Master Batch Records, change controls, GMP documentation and operational risk assessments.

You will support technology transfers, pre-campaign readiness and manufacturing training activities, partnering closely with Manufacturing, Quality and Engineering teams. A key aspect of the role will be managing manufacturing deviations, CAPAs, investigation actions, rejected materials and related follow-up activities.

You will lead or support root-cause, product-impact and trend investigations, contribute to deviation review forums, and ensure actions are completed to enable timely lot disposition and product release. You will also support audit readiness and the timely resolution of audit observations.

Requirements

The successful candidate will hold a degree in Engineering, Biotechnology, Life Sciences or a related discipline, with relevant experience gained in a GMP pharmaceutical or biologics manufacturing environment.

You should possess a sound understanding of manufacturing processes, equipment and GMP documentation requirements. Hands-on experience in Master Batch Records, deviations, CAPAs, change controls, risk assessments and root-cause investigations is essential.

Candidates should demonstrate strong technical writing, communication and stakeholder-management skills, with the ability to work independently and manage changing priorities in a fast-paced manufacturing environment.

To Apply

To apply, please submit your resume to Tahmid Bin Zafar at [Confidential Information], citing reference number TZ36382. We regret to inform that only shortlisted candidates will be notified.

Desired Skills and Experience

Pharmaceutical Manufacturing · GMP Documentation · Deviation & Investigation Management · CAPA and Change Control · Technology Transfer & Campaign Readiness