QC Technologist/Documentation Coordinator

3 days ago

Slough, United Kingdom SRG Full time

Job title: Technologist/Documentation CoordinatorLocation: SloughContract Length: 6 monthsWorking Hours: 37.5 hours/weekPay Rate: £14.42 p/hAbout the RoleTo be able to work effectively within the QC Raw Materials team, maintaining required timelines with general guidance and supportFlawless 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 environmentProvide 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 TeamKey ResponsibilitiesTesting of samples and reporting of all results according to relevant GMP procedures if requiredAdd results generated by other team membersAct 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 ideasSome 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-BScField of Study-Pharmaceutical Sciences, ChemistryWork Experience GMP Lab environment with the Pharma IndustryLevel-Entry Level - 0-4 yearsGuidant,

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