2 jobs found in sittingbourne, kent

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    • sittingbourne, kent
    • permanent
    • £30,000 - £35,000 per year
    • full-time
    Quality Assurance Officer My Client, an established pharmaceutical manufacturing business has a requirement through expansion for a Quality Officer at their Queenbourgh site. As Quality Officer, you will:Ensure that all activities within Development are undertaken to established standards of GMPAssist in internal/external quality audits. Ensure implementation of resulting improvement recommendations or compliance gaps, in accordance with the site Quality System process.To assist in ensuring that all deviations are reported and investigated with corrective actions completed to agreed timescales.Work with Development Centre in developing reports on quality issues e.g. deviations, batch failures, etc. To Be considered for the role of Quality Officer, you will:Educated to degree level in a related scientific fieldKnowledge of Microsoft Office software.ERP software experience preferable.Demonstrate a good understanding of GMP for IMP and developmentInvestigational Medicinal Products This is a permanent position based in Queenborough, Kent. You will need to be able to commute and hold current, valid right to work status. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    Quality Assurance Officer My Client, an established pharmaceutical manufacturing business has a requirement through expansion for a Quality Officer at their Queenbourgh site. As Quality Officer, you will:Ensure that all activities within Development are undertaken to established standards of GMPAssist in internal/external quality audits. Ensure implementation of resulting improvement recommendations or compliance gaps, in accordance with the site Quality System process.To assist in ensuring that all deviations are reported and investigated with corrective actions completed to agreed timescales.Work with Development Centre in developing reports on quality issues e.g. deviations, batch failures, etc. To Be considered for the role of Quality Officer, you will:Educated to degree level in a related scientific fieldKnowledge of Microsoft Office software.ERP software experience preferable.Demonstrate a good understanding of GMP for IMP and developmentInvestigational Medicinal Products This is a permanent position based in Queenborough, Kent. You will need to be able to commute and hold current, valid right to work status. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    • sittingbourne, kent
    • permanent
    • £35,000 - £50,000 per year
    • full-time
    QC Laboratory Validation Specialist My Client, an independent Pharmaceutical business has a great opportunity for an experienced Laboratory Validation specialist to join their business in Kent. The Quality Control Laboratory Validation Specialist is responsible for the oversight of the qualification status and maintenance of the laboratory's instrumentation and operational equipment and reports to the QA & Compliance Manager. You will be responsible for establishing and maintaining suitable systems to allow the visibility and tracking of instrument availability, qualification / calibration status, scheduling of planned maintenance activities, and rapid resolution of breakdowns to ensure the Quality Control department is properly supported and able to execute testing requirements. Experience required: Trackwise, Empower, Tiamo 2.5, WinLab UV, TruScan 2.6.0, TOC DataPro900 0.1.51, Spectrum 2, Lab Network, LabX, SEAL CSFAs, Agilent Baths.Ensure GMP environment systems and software validation and process compliance with internal policies and external (Data Integrity, FDA, ICH and MHRA) regulations. Ensure QC Systems and data comply with Data Integrity regulations. Whilst the role is not specifically required to execute repair / maintenance work directly on / to the QC instrumentation / equipment / software, there is an expectation that the role will maintain a suitable level of technical competence to conduct or assist in identifying faults and causes to facilitate rapid resolution.This is a permanent position based in Queenborugh, Kent. Valid Right to work status required or application will not be considered. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    QC Laboratory Validation Specialist My Client, an independent Pharmaceutical business has a great opportunity for an experienced Laboratory Validation specialist to join their business in Kent. The Quality Control Laboratory Validation Specialist is responsible for the oversight of the qualification status and maintenance of the laboratory's instrumentation and operational equipment and reports to the QA & Compliance Manager. You will be responsible for establishing and maintaining suitable systems to allow the visibility and tracking of instrument availability, qualification / calibration status, scheduling of planned maintenance activities, and rapid resolution of breakdowns to ensure the Quality Control department is properly supported and able to execute testing requirements. Experience required: Trackwise, Empower, Tiamo 2.5, WinLab UV, TruScan 2.6.0, TOC DataPro900 0.1.51, Spectrum 2, Lab Network, LabX, SEAL CSFAs, Agilent Baths.Ensure GMP environment systems and software validation and process compliance with internal policies and external (Data Integrity, FDA, ICH and MHRA) regulations. Ensure QC Systems and data comply with Data Integrity regulations. Whilst the role is not specifically required to execute repair / maintenance work directly on / to the QC instrumentation / equipment / software, there is an expectation that the role will maintain a suitable level of technical competence to conduct or assist in identifying faults and causes to facilitate rapid resolution.This is a permanent position based in Queenborugh, Kent. Valid Right to work status required or application will not be considered. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

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