QC Technologist
SRG is looking for an QC Technologist in Slough
Job description
- Job title: Technologist/Documentation Coordinator
- Location: Slough
- Contract Length: 6 months
- Working Hours: 37.5 hours/week
- Pay Rate: £14.42 p/h
About the Role
- 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
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 sites 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.
Skills/Competencies
- 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.
Education
- Preferred-BSc
- Field of Study-Pharmaceutical Sciences, Chemistry
Work Experience
- GMP Lab environment with the Pharma Industry
- Level-Entry Level - 0-4 years
Extra information
- Status
- Open
- Education Level
- Secondary School
- Location
- Slough
- Type of Contract
- Part-time jobs
- Published at
- 29-12-2025
- Full UK/EU driving license preferred
- No
- Car Preferred
- No
- Must be eligible to work in the EU
- No
- Cover Letter Required
- No
- Languages
- English
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