Laura Sharpe laura@pfizer.com & | Highly innovative and motivated individual having worked across various industries and skill sectors spanning 25 years, for example; Leisure, Retail, NHS, Academia, Science and Research and now Pharma. Each experience shows a proven track record of year on year targets achieved, process improvements made and deliverables met. I have been successful in each area, by applying my transferable skill set with a flexible approach and adapting to each role as necessary. This has now lead me into the world of cold chain validation, working as part of a dynamic team in Temperature Controlled Logistics (TCL) at Pfizer. Having worked at Pfizer since Jan 2017 as a validation specialist gaining much knowledge and allowing me to further expand my skillset during this time. Attendence at FAT in order to test a new line to bring to site as well as new product introduction. Development of IQ,OQ and PQ protocols in order to support testing at site. Execution of protocols to ensure validation and GMP regulatory compliance. Development of decommissioning plan and protocols in order to ensure compliant decommissioning. I have a full understanding of the validation lifecycle and the importance of working in a GMP regultory environment. I have a strong sense of leadership and great communication skills and I am expirenced in playing a key role in multi-functional environments and communicating and collaborating with a broad range of people at all levels both internally and externally as well as internationally. I have over 13 years’ experience in Clinical trials, including sample, operations and logistics management, Laboratory Information Management Systems (LIMS) management and in cold chain storage of samples (Cryopreservation). BioBank Management of over 500,000+ clinical trial samples. I possess extensive knowledge and solid technical skills in laboratory and sample management processes, as well as project management fundamentals (lean six sigma yellow belt). I enjoy applying my skill set to new areas and expanding on these skills and I thrive on new challenges.

Laura Sharpe

Highly innovative and motivated individual having worked across various industries and skill sectors spanning 25 years, for example;...

United Kingdom

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Laura Sharpe’s Emails [email protected]

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Laura Sharpe’s Location United Kingdom

Laura Sharpe’s Expertise Highly innovative and motivated individual having worked across various industries and skill sectors spanning 25 years, for example; Leisure, Retail, NHS, Academia, Science and Research and now Pharma. Each experience shows a proven track record of year on year targets achieved, process improvements made and deliverables met. I have been successful in each area, by applying my transferable skill set with a flexible approach and adapting to each role as necessary. This has now lead me into the world of cold chain validation, working as part of a dynamic team in Temperature Controlled Logistics (TCL) at Pfizer. Having worked at Pfizer since Jan 2017 as a validation specialist gaining much knowledge and allowing me to further expand my skillset during this time. Attendence at FAT in order to test a new line to bring to site as well as new product introduction. Development of IQ,OQ and PQ protocols in order to support testing at site. Execution of protocols to ensure validation and GMP regulatory compliance. Development of decommissioning plan and protocols in order to ensure compliant decommissioning. I have a full understanding of the validation lifecycle and the importance of working in a GMP regultory environment. I have a strong sense of leadership and great communication skills and I am expirenced in playing a key role in multi-functional environments and communicating and collaborating with a broad range of people at all levels both internally and externally as well as internationally. I have over 13 years’ experience in Clinical trials, including sample, operations and logistics management, Laboratory Information Management Systems (LIMS) management and in cold chain storage of samples (Cryopreservation). BioBank Management of over 500,000+ clinical trial samples. I possess extensive knowledge and solid technical skills in laboratory and sample management processes, as well as project management fundamentals (lean six sigma yellow belt). I enjoy applying my skill set to new areas and expanding on these skills and I thrive on new challenges.

Laura Sharpe’s Current Industry Pfizer

Laura Sharpe’s Prior Industry
Imperial College London | Pfizer

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Work Experience

Pfizer

Senior Manager Transport Validation and Innovation

Thu Jun 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Pfizer

Transport Qualification Manager

Sat Oct 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jun 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)

Pfizer

Transport Qualification Specialist

Mon Mar 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Oct 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Pfizer

Validation Specialist

Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Mar 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)

Imperial College London

Sample Logistics and Distribution Manager

Sun Oct 01 2000 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Dec 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)

Skills

Languages

FAQ About Laura Sharpe

Laura Sharpe is located at
United Kingdom

Laura Sharpe is a
Highly innovative and motivated individual having worked across various industries and skill sectors spanning 25 years, for example; Leisure, Retail, NHS, Academia, Science and Research and now Pharma. Each experience shows a proven track record of year on year targets achieved, process improvements made and deliverables met. I have been successful in each area, by applying my transferable skill set with a flexible approach and adapting to each role as necessary. This has now lead me into the world of cold chain validation, working as part of a dynamic team in Temperature Controlled Logistics (TCL) at Pfizer. Having worked at Pfizer since Jan 2017 as a validation specialist gaining much knowledge and allowing me to further expand my skillset during this time. Attendence at FAT in order to test a new line to bring to site as well as new product introduction. Development of IQ,OQ and PQ protocols in order to support testing at site. Execution of protocols to ensure validation and GMP regulatory compliance. Development of decommissioning plan and protocols in order to ensure compliant decommissioning. I have a full understanding of the validation lifecycle and the importance of working in a GMP regultory environment. I have a strong sense of leadership and great communication skills and I am expirenced in playing a key role in multi-functional environments and communicating and collaborating with a broad range of people at all levels both internally and externally as well as internationally. I have over 13 years’ experience in Clinical trials, including sample, operations and logistics management, Laboratory Information Management Systems (LIMS) management and in cold chain storage of samples (Cryopreservation). BioBank Management of over 500,000+ clinical trial samples. I possess extensive knowledge and solid technical skills in laboratory and sample management processes, as well as project management fundamentals (lean six sigma yellow belt). I enjoy applying my skill set to new areas and expanding on these skills and I thrive on new challenges. Pfizer

Laura Sharpe currently works in the
Pfizer

Laura Sharpe specializes in
Highly innovative and motivated individual having worked across various industries and skill sectors spanning 25 years, for example; Leisure, Retail, NHS, Academia, Science and Research and now Pharma. Each experience shows a proven track record of year on year targets achieved, process improvements made and deliverables met. I have been successful in each area, by applying my transferable skill set with a flexible approach and adapting to each role as necessary. This has now lead me into the world of cold chain validation, working as part of a dynamic team in Temperature Controlled Logistics (TCL) at Pfizer. Having worked at Pfizer since Jan 2017 as a validation specialist gaining much knowledge and allowing me to further expand my skillset during this time. Attendence at FAT in order to test a new line to bring to site as well as new product introduction. Development of IQ,OQ and PQ protocols in order to support testing at site. Execution of protocols to ensure validation and GMP regulatory compliance. Development of decommissioning plan and protocols in order to ensure compliant decommissioning. I have a full understanding of the validation lifecycle and the importance of working in a GMP regultory environment. I have a strong sense of leadership and great communication skills and I am expirenced in playing a key role in multi-functional environments and communicating and collaborating with a broad range of people at all levels both internally and externally as well as internationally. I have over 13 years’ experience in Clinical trials, including sample, operations and logistics management, Laboratory Information Management Systems (LIMS) management and in cold chain storage of samples (Cryopreservation). BioBank Management of over 500,000+ clinical trial samples. I possess extensive knowledge and solid technical skills in laboratory and sample management processes, as well as project management fundamentals (lean six sigma yellow belt). I enjoy applying my skill set to new areas and expanding on these skills and I thrive on new challenges.