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

Slough | Part-time jobs | Secondary School

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