2 jobs found in 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.
    • queenborough, kent
    • permanent
    • £40,000 - £60,000 per year
    • part-time
    My Client, an established Pharmaceutical company has a great opportunity for a Quality Manager to join their QA Team on a Permanent, part time basis. To lead and control activities of the Development Quality Team in line with both Development and Quality requirements to ensure that all products developed and produced as Clinical or investigations materials comply with regulatory and quality standards. As Quality Manager, you will: Contributes, and where applicable facilitates the resolution of operational problems in Development whilst maintaining compliance to cGMP and license commitments. Ensures in conjunction with Compliance Manager that all quality systems are managed appropriately, compliant to GMP and fit for purpose these include Deviation Management CAPA Management Complaint Management Level 1 and 2 Audits have been conducted in accordance with predefined schedules e. Host customer and regulatory audits Provide oversight and support for day to day customer queries Provide support and mentoring for Quality Officers Batch Record Review Initiation and management of QTAs Provides a day - to - day contact, aiming for consistency in approach for quality related issues for Development through direct review of operational areas and practices 4. Liaise with Project Managers to ensure that time-lines are met and regulatory compliance is maintained Liaise with Donor laboratories, Development Laboratory, Analytical Development Group and QC Laboratory for method transfer and validation for raw materials and finished product Implements policies and procedures relating to Regulatory and cGMP. Knowledge & Experience Required: Science degree and at least 10 years relevant experience within the pharmaceutical industry. At least 5 years at management level with demonstrated experience An in-depth knowledge of the appropriate European, US regulations Experience in Pharmaceutical Production. Experience of production of Investigational Medicinal Products This is a Part Tine position, minimum of 24 hours per week. Salary Prorata. 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.
    My Client, an established Pharmaceutical company has a great opportunity for a Quality Manager to join their QA Team on a Permanent, part time basis. To lead and control activities of the Development Quality Team in line with both Development and Quality requirements to ensure that all products developed and produced as Clinical or investigations materials comply with regulatory and quality standards. As Quality Manager, you will: Contributes, and where applicable facilitates the resolution of operational problems in Development whilst maintaining compliance to cGMP and license commitments. Ensures in conjunction with Compliance Manager that all quality systems are managed appropriately, compliant to GMP and fit for purpose these include Deviation Management CAPA Management Complaint Management Level 1 and 2 Audits have been conducted in accordance with predefined schedules e. Host customer and regulatory audits Provide oversight and support for day to day customer queries Provide support and mentoring for Quality Officers Batch Record Review Initiation and management of QTAs Provides a day - to - day contact, aiming for consistency in approach for quality related issues for Development through direct review of operational areas and practices 4. Liaise with Project Managers to ensure that time-lines are met and regulatory compliance is maintained Liaise with Donor laboratories, Development Laboratory, Analytical Development Group and QC Laboratory for method transfer and validation for raw materials and finished product Implements policies and procedures relating to Regulatory and cGMP. Knowledge & Experience Required: Science degree and at least 10 years relevant experience within the pharmaceutical industry. At least 5 years at management level with demonstrated experience An in-depth knowledge of the appropriate European, US regulations Experience in Pharmaceutical Production. Experience of production of Investigational Medicinal Products This is a Part Tine position, minimum of 24 hours per week. Salary Prorata. 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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