* 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
o To be able to work effectively within the QC Raw Materials team, maintaining required timelines with general guidance and support
o 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
o Provide support to more junior members of staff, ensuring high standards of quality are being maintained throughout the department.
o To Coordinate everyday job when required within the Raw Materials Team
Key Responsibilities
o Testing of samples and reporting of all results according to relevant GMP procedures if required
o Add results generated by other team members
o Act in accordance with all safety requirements relevant to the tasks being performed.
o Continuously identify, assess and implement improvements in GMP compliance, safety and efficiency.
o Manage the archiving of assay forms and Raw Materials Specification (RMS).
o Prepare and send RMS releases packs to other sites or inter customer audits and provide documentation for internal audits as required.
o Supply vendor certification upon request.
o Take ownership of processing RMS for release, ensuring accuracy and compliance.
o Support the monthly retain audit process.
o Be in control of own schedule with general direction from Group Leader/Schedulers and able to complete work in required timelines.
o Be able to manage, change effectively and escalate any delays to QC management.
Skills/Competencies
o 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
o Some chemical / Biochemical techniques and methods. Reporting of data. Quality records. Ability to maintain a high standard of work when required.
o 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.
o 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.
o Ability to deliver work / projects to agreed timelines whilst maintaining a high standard of quality.
o Demonstrates loyalty and commitment to the team, supportive. Train and assist more junior members of staff.
Education
o Preferred-BSc
o Field of Study-Pharmaceutical Sciences, Chemistry
Work Experience
o GMP Lab environment with the Pharma Industry
o Level-Entry Level - 0-4 years