Technologist

Summary: The Technologist/Documentation Coordinator role in Slough involves testing samples and reporting results in compliance with GMP procedures. The position requires managing documentation, supporting audits, and ensuring safety and efficiency in a GMP lab environment within the pharmaceutical industry. The candidate will also be responsible for processing RMS for release and managing their schedule effectively. A degree in Chemistry is preferred, with some experience in a laboratory setting being advantageous.

Key Responsibilities:

• Testing of samples and reporting of all results according to relevant GMP procedures if required
• Add results generated by other team members
• Act in accordance with all safety requirements relevant to the tasks being performed
• Continuously identify, assess and implement improvements in GMP compliance, safety and efficiency
• Manage the archiving of assay forms and Raw Materials Specification (RMS)
• Prepare and send RMS releases packs to other site or inter customer audits and provide documentation for internal audits as required
• Supply vendor certification upon request
• Take ownership of processing RMS for release, ensuring accuracy and compliance
• Support the monthly retain audit process
• Be in control of own schedule with general direction from Group Leader/Schedulers and able to complete work in required timelines
• Be able to manage change effectively and escalate any delays to QC management

Key Skills:

• Chemistry degree, preferably BSc
• Knowledge of GMP and laboratory environment
• Familiarity with chemical/biochemical techniques and methods
• Data reporting skills
• Ability to manage schedules and work timelines
• Effective communication and escalation skills

Salary (Rate): undetermined

City: Slough

Country: United Kingdom

Working Arrangements: on-site

IR35 Status: undetermined

Seniority Level: undetermined

Industry: Other