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Project manager - GMP peptide services
Project manager - GMP peptide services
Project manager - GMP peptide services
Posted 8 days ago
- Leicester, Leicestershire
- Any
- External
We take great pride in our vast range of chemical and biochemical products, and our high standards are maintained through great people, who share our values, and want to do the very best job possible, every day.
We acknowledge the important part our team members, who are based over three continents with manufacturing laboratories in Switzerland, the United Kingdom, Slovakia and China, and distribution centres in the United States, play, in our continued success.
Main Purpose of the Job
To work as part of the GMP Peptide Services Team and to support the GMP sales process as well as acting as a Project Manager during project execution.
Key Responsibilities
Support the GMP sales process – by joining in customer (acquisition) calls as specialists – and prepare the proposals (quoting) as well.
Project manager is responsible for customer communication during project execution – and as such for customer experience.
Initiating and guiding of production process (including associated documentation) for GMP/PM projects.
Preparing of the necessary documentation for GMP and PM projects.
Representation of Operations in project team meetings.
Supporting the development of new GMP and PM processes.
Supporting the development of new methodologies and processes
Other duties as assigned.
Employee works in conformity with the installed quality assurance system ISO 9001 and GMP-API.
Candidate Requirements
Minimum education of Master's degree in relevant field (organic chemistry/peptide chemistry) ideally educated to PhD level
Previous experience in a similar role would be required
Excellent spoken and written command of the English language
Good theoretical and practical knowledge of the relevant professional field
Thorough knowledge of GMP
Software skills, e.g. Office, SAP etc.
Excellent social skills, structural / independent working attitude, team player
Experience with QMS system would be desirable but not essential
About us
Biosynth® is an innovative life sciences reagents, custom synthesis and manufacturing services company headquartered in Staad, Switzerland. We are by scientists, for scientists, securing supply chains with consistent quality, across the globe. As a trusted supplier, manufacturer and partner to the pharmaceutical, life science and diagnostic industries, as well as food, agrochemical and cosmetic customers, we have facilities on three continents and a rapid global distribution network. Our main production laboratories are located in Switzerland, the UK, Slovakia and China, with peptide and antibody production in the US, the UK and the Netherlands. Enzyme projects are based in Austria, bioconjugation projects in Germany and biological IVD reagents in Ireland.
Recruitment agencies - We do not use external recruitment agencies to recruit for any of our positions. We will not accept unsolicited CVs and communications from external recruiters.
We acknowledge the important part our team members, who are based over three continents with manufacturing laboratories in Switzerland, the United Kingdom, Slovakia and China, and distribution centres in the United States, play, in our continued success.
Main Purpose of the Job
To work as part of the GMP Peptide Services Team and to support the GMP sales process as well as acting as a Project Manager during project execution.
Key Responsibilities
Support the GMP sales process – by joining in customer (acquisition) calls as specialists – and prepare the proposals (quoting) as well.
Project manager is responsible for customer communication during project execution – and as such for customer experience.
Initiating and guiding of production process (including associated documentation) for GMP/PM projects.
Preparing of the necessary documentation for GMP and PM projects.
Representation of Operations in project team meetings.
Supporting the development of new GMP and PM processes.
Supporting the development of new methodologies and processes
Other duties as assigned.
Employee works in conformity with the installed quality assurance system ISO 9001 and GMP-API.
Candidate Requirements
Minimum education of Master's degree in relevant field (organic chemistry/peptide chemistry) ideally educated to PhD level
Previous experience in a similar role would be required
Excellent spoken and written command of the English language
Good theoretical and practical knowledge of the relevant professional field
Thorough knowledge of GMP
Software skills, e.g. Office, SAP etc.
Excellent social skills, structural / independent working attitude, team player
Experience with QMS system would be desirable but not essential
About us
Biosynth® is an innovative life sciences reagents, custom synthesis and manufacturing services company headquartered in Staad, Switzerland. We are by scientists, for scientists, securing supply chains with consistent quality, across the globe. As a trusted supplier, manufacturer and partner to the pharmaceutical, life science and diagnostic industries, as well as food, agrochemical and cosmetic customers, we have facilities on three continents and a rapid global distribution network. Our main production laboratories are located in Switzerland, the UK, Slovakia and China, with peptide and antibody production in the US, the UK and the Netherlands. Enzyme projects are based in Austria, bioconjugation projects in Germany and biological IVD reagents in Ireland.
Recruitment agencies - We do not use external recruitment agencies to recruit for any of our positions. We will not accept unsolicited CVs and communications from external recruiters.