QC Technologist

Job Details

• Job title: Technologist/Documentation Coordinator
• Location: Slough
• Working Hours: 37.5 hours/week

• To be able to work effectively within the QC Raw Materials team, maintaining required timelines with general guidance and support
• Flawless execution of work with the ability to adapt to change to produce high quality work in accordance with the expectations of working within a GMP custom manufacturing environment
• Provide support to more junior members of staff, ensuring high standards of quality are being maintained throughout the department.
• To Coordinate everyday job when required within the Raw Materials Team

• 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 sites or inter customer audits and provide documentation for internal audits as required.
• 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 elevate any delays to QC management.
• Ability to adapt to change. Willing to undertake a range of tasks for the effective running of the department. Proactive - Anticipates problems and shows initiative for problem-solving and generating new ideas
• Some chemical / Biochemical techniques and methods. Reporting of data. Quality records. Ability to maintain a high standard of work when required.
• Ability to review data and ensure high standards are being adhered to by other members of staff. Ability to work well alone and within a team. Willing to work with others to achieve the common goal.
• Actively promotes the department. Able to deal with confidential information in an appropriate and sensitive way. Does not divulge confidential information outside of the department / company.
• Ability to deliver work / projects to agreed timelines whilst maintaining a high standard of quality.
• Demonstrates loyalty and commitment to the team, supportive. Train and assist more junior members of staff.

• Preferred-BSc
• Field of Study-Pharmaceutical Sciences, Chemistry

• GMP Lab environment with the Pharma Industry
• Level-Entry Level - 0-4 years

Associate

Temporary

Quality Assurance and Science

Pharmaceutical Manufacturing