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4 jobs found for biotechnology & pharmaceutical

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    • maidenhead, berkshire
    • contract
    • £50.00 - £75.00, per hour, Depending on experience
    • full-time
    Do you have 3 years pharmaceutical/biotechnology industry experience in International/Regulatory Emerging Markets?Are you passionate about regulatory affairs? My Client, a leading Pharma Biotech has a great opportunity for an Senior Manager, Regulatory Affairs -International Growth Markets on a 12 month contract based in Maidenhead. As Senior RA Manager IGM, you will:Responsible for driving development and implementation of International Growth Market (IGM) regulatory strategies for all new product registration submissions and lifecycle management activities in the CEER region including Israel, Russia, Turkey.Represent IGM Regulatory on the global regulatory project teams representing the International Growth markets (APAC, LATAM, MART regions) for 1-3 marketed products.To Be considered for the role of Senior RA Manager IGM, you will:Minimum 3 years Pharma/biotech experience in International/Regulatory Emerging MarketsSkills and experience to represent the IGM group on project teams.Experience in the preparation of major regulatory submissions supportive amendments, supplements and labelling lifecycle management.Good knowledge and understanding of applicable regions (Russia, Turkey, Israel preferred).This is an INSIDE IR35 role. 12 Month Contract. Valid Right to work status required. 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.
    Do you have 3 years pharmaceutical/biotechnology industry experience in International/Regulatory Emerging Markets?Are you passionate about regulatory affairs? My Client, a leading Pharma Biotech has a great opportunity for an Senior Manager, Regulatory Affairs -International Growth Markets on a 12 month contract based in Maidenhead. As Senior RA Manager IGM, you will:Responsible for driving development and implementation of International Growth Market (IGM) regulatory strategies for all new product registration submissions and lifecycle management activities in the CEER region including Israel, Russia, Turkey.Represent IGM Regulatory on the global regulatory project teams representing the International Growth markets (APAC, LATAM, MART regions) for 1-3 marketed products.To Be considered for the role of Senior RA Manager IGM, you will:Minimum 3 years Pharma/biotech experience in International/Regulatory Emerging MarketsSkills and experience to represent the IGM group on project teams.Experience in the preparation of major regulatory submissions supportive amendments, supplements and labelling lifecycle management.Good knowledge and understanding of applicable regions (Russia, Turkey, Israel preferred).This is an INSIDE IR35 role. 12 Month Contract. Valid Right to work status required. 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.
    • maidenhead, berkshire
    • contract
    • £40.00 - £48.00 per hour
    • full-time
    Responsible for all local Pharmacovigilance-related activities for provision of safety report handling relating to Development and maintenance of local PV processes and procedures.As PV Scientist, you will: Reviewing local and national legislation (MHRA or HPRA) to maintain an awareness of local regulations and ensuring local processes are aligned Notifying Global Drug Safety of any programmes/contractual arrangements with external providers with significance for handling AE information Monitoring the MHRA portal for safety reports To be considered for the role of PV Scientist, you will:At least 5 years experience in Drug safety/ Pharmacovigilance in a Pharmaceutical businessDrafting and Revising safety detailsextensive PV affiliate experience beyond just ICSR managementRSG Database 12 Month Contract, full time. This is an Inside IR35 role, based in Maidenhead. 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.
    Responsible for all local Pharmacovigilance-related activities for provision of safety report handling relating to Development and maintenance of local PV processes and procedures.As PV Scientist, you will: Reviewing local and national legislation (MHRA or HPRA) to maintain an awareness of local regulations and ensuring local processes are aligned Notifying Global Drug Safety of any programmes/contractual arrangements with external providers with significance for handling AE information Monitoring the MHRA portal for safety reports To be considered for the role of PV Scientist, you will:At least 5 years experience in Drug safety/ Pharmacovigilance in a Pharmaceutical businessDrafting and Revising safety detailsextensive PV affiliate experience beyond just ICSR managementRSG Database 12 Month Contract, full time. This is an Inside IR35 role, based in Maidenhead. 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.
    • maidenhead, berkshire
    • contract
    • £55,000 per year
    • full-time
    Job title: Contracts & Tenders Manager, UK & IrelandLocation: MaidenheadPay rate: £55,000Contract We are recruiting on behalf of a global healthcare organisation, for a Contracts & Tenders Manager to provide commercial support and advice to the sales teams . The ideal candidate will have a good understanding of the procurement within the UK and experience in contract management. Responsibilities:The Tenders & Contracts Manager is a key business partner that enables the business demands to be met in a fully compliant, effective and efficient manner.To manage all Tenders and Contract knowledge to ensure there us a market picture readily available.To be a permanent advisor to sales, marketing and general management in relation to all process offerings.To ensure all price offerings are submitted on time are of a high quality. Requirements:Has a good understanding of the procurement process within the UK.Previous experience in a commercial environment is an advantage but not essential.Excellent verbal and written communication skills in English and local language.Good experience in use of analytical tools and software.Ability to work effectively within a team in a fast-paced changing environment.Bachelor's degree in medical / mechanical or medical technology is preferred or working.experience in a similar position.This role will require the management of 2/3 direct reports so experience in leading a team would be preferred.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
    Job title: Contracts & Tenders Manager, UK & IrelandLocation: MaidenheadPay rate: £55,000Contract We are recruiting on behalf of a global healthcare organisation, for a Contracts & Tenders Manager to provide commercial support and advice to the sales teams . The ideal candidate will have a good understanding of the procurement within the UK and experience in contract management. Responsibilities:The Tenders & Contracts Manager is a key business partner that enables the business demands to be met in a fully compliant, effective and efficient manner.To manage all Tenders and Contract knowledge to ensure there us a market picture readily available.To be a permanent advisor to sales, marketing and general management in relation to all process offerings.To ensure all price offerings are submitted on time are of a high quality. Requirements:Has a good understanding of the procurement process within the UK.Previous experience in a commercial environment is an advantage but not essential.Excellent verbal and written communication skills in English and local language.Good experience in use of analytical tools and software.Ability to work effectively within a team in a fast-paced changing environment.Bachelor's degree in medical / mechanical or medical technology is preferred or working.experience in a similar position.This role will require the management of 2/3 direct reports so experience in leading a team would be preferred.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
    • witney, oxfordshire
    • contract
    • £11.59 per hour
    • full-time
    Randstad is recruiting for a Lab Technician on behalf of a global medical device and health care leader, who are dedicated to helping people reach their full health potential. The successful candidate will have great attention to detail, be able to pick up the nature of the role quickly and be able to deliver quality and compliant products in a timely manner.Key Responsibilities:* Perform sampling, inspections, sensor testing, batch record review and approval* Perform inspections associated with laboratory investigations and / or technical / quality system investigations and generate associated reports* To visually inspect products (or with the use of specified instruments) as directed,for defects or imperfections in accordance with the relevant Standard Operating Procedures (SOP's)* Managing the product retain process, placing product lots into applicable storage conditions and coordinating the timely destruction of products at the end of their retention periodKey Requirements:* Excellent attention to detail* Experience in a similar role would be advantageous * Good problem solving abilities* Basic IT skills* Secondary education - Maths and English GCSE Please apply with an up to date CV and we will be in touch shortly. Randstad Business Support is acting as an Employment Business in relation to this vacancy.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
    Randstad is recruiting for a Lab Technician on behalf of a global medical device and health care leader, who are dedicated to helping people reach their full health potential. The successful candidate will have great attention to detail, be able to pick up the nature of the role quickly and be able to deliver quality and compliant products in a timely manner.Key Responsibilities:* Perform sampling, inspections, sensor testing, batch record review and approval* Perform inspections associated with laboratory investigations and / or technical / quality system investigations and generate associated reports* To visually inspect products (or with the use of specified instruments) as directed,for defects or imperfections in accordance with the relevant Standard Operating Procedures (SOP's)* Managing the product retain process, placing product lots into applicable storage conditions and coordinating the timely destruction of products at the end of their retention periodKey Requirements:* Excellent attention to detail* Experience in a similar role would be advantageous * Good problem solving abilities* Basic IT skills* Secondary education - Maths and English GCSE Please apply with an up to date CV and we will be in touch shortly. Randstad Business Support is acting as an Employment Business in relation to this vacancy.Randstad Business Support is acting as an Employment Business in relation to this vacancy.

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