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2 jobs found in Maidenhead, Berkshire

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    • maidenhead, berkshire
    • contract
    • £45.00 - £55.00, per hour, Depending on experience
    • full-time
    My client, a leading Pharma Biotech has an exciting opportunity for an experienced Regulatory Affairs Manager to join their team in Maidenhead on a 6 Month contract. As Regulatory Affairs Manager, you will:Define strategies for meeting and keeping post-approval compliance. Responsible for regulatory documents, submissions, and compliance issues.Provide strategic guidance and regulatory leadership at project team meetings as well as represent the Global Emerging Markets strategy for assigned products in the region. Identify and assess regulatory risks associated with the execution of regulatory strategies in assigned regions. Define strategies to mitigate risks. o Keep abreast of changes in regional legislation. - To be considered for the position of Regulatory Affairs Manager, you will have:Minimum 7 years pharmaceutical/biotech industry experience5 years of Regulatory Affairs experienceEducated to degree level in a related Life science field This is an Inside IR35 contract position, via Randstad. 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, a leading Pharma Biotech has an exciting opportunity for an experienced Regulatory Affairs Manager to join their team in Maidenhead on a 6 Month contract. As Regulatory Affairs Manager, you will:Define strategies for meeting and keeping post-approval compliance. Responsible for regulatory documents, submissions, and compliance issues.Provide strategic guidance and regulatory leadership at project team meetings as well as represent the Global Emerging Markets strategy for assigned products in the region. Identify and assess regulatory risks associated with the execution of regulatory strategies in assigned regions. Define strategies to mitigate risks. o Keep abreast of changes in regional legislation. - To be considered for the position of Regulatory Affairs Manager, you will have:Minimum 7 years pharmaceutical/biotech industry experience5 years of Regulatory Affairs experienceEducated to degree level in a related Life science field This is an Inside IR35 contract position, via Randstad. 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
    • £18.00 - £23.00, per hour, Depending on experience
    • full-time
    My client, a leading Pharma Biotech, has a requirement for a Regulatory Affairs administrator to join their small team on a 12 month contract at their Maidenhead site. As RA Administrator, you will:Regulatory administration tasks; Coordinate and execute end-to-end changes for existing portfolio of products and support the launch of new products - e.g Change control, artworks, label updates etc. Work closely with internal stakeholders to update them on any changes to the existing portfolio and new product launches.Maintain oversight of ongoing regulatory procedures and pro-actively coordinate these To be considered for the RA Administrator role, you will:1-3 years years working experience in the Regulatory fieldRelevant technical experience - e.g. MTA, PTA, CTAPharma/ Biopharma experience Very strong organisational skills]A strong want to develop in a regulatory affairs environment This is a 12 month PAYE contract based in Maidenhead. Remote/ hybrid working 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.
    My client, a leading Pharma Biotech, has a requirement for a Regulatory Affairs administrator to join their small team on a 12 month contract at their Maidenhead site. As RA Administrator, you will:Regulatory administration tasks; Coordinate and execute end-to-end changes for existing portfolio of products and support the launch of new products - e.g Change control, artworks, label updates etc. Work closely with internal stakeholders to update them on any changes to the existing portfolio and new product launches.Maintain oversight of ongoing regulatory procedures and pro-actively coordinate these To be considered for the RA Administrator role, you will:1-3 years years working experience in the Regulatory fieldRelevant technical experience - e.g. MTA, PTA, CTAPharma/ Biopharma experience Very strong organisational skills]A strong want to develop in a regulatory affairs environment This is a 12 month PAYE contract based in Maidenhead. Remote/ hybrid working 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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