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Senior Principal Scientist - Analytical Development

SRG
Posted 16 days ago, valid for 9 days
Location

Macclesfield, Cheshire SK117UX, England

Salary

£60,000 - £72,000 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The position is for a Senior Principal Scientist in Analytical Science at a growing pharmaceutical development company located in South Manchester, with a negotiable salary.
  • Candidates must have a PhD and over 5 years of experience in pharmaceutical sciences and drug development, or a bachelor's degree with over 10 years of experience.
  • The role involves ensuring excellence in analytical science, driving client projects, mentoring junior staff, and staying updated with technological advances.
  • Responsibilities include developing analytical methods, managing global regulatory requirements, and acting as a project leader for client projects.
  • Occasional travel within the UK and abroad will be required for client meetings and business development events.

Job Title: Senior Principal Scientist - Analytical ScienceDepartment: Pharmaceutical DevelopmentLine Manager: Team Director

Salary: NegotiableLocation: South Manchester (occasional travel will be required to attend client meetings, CRO visits and business development events across the UK and potentially abroad. Occasional overnight stays will be required).

SRG are working exclusively with a rapidly growing pharmaceutical development company that's looking to expand and take on a new Senior Principal Scientist in Analytical Development department.

Job purpose:The primary purpose of this role is to ensure excellence in company's analytical science provision. You have responsibility for driving the analytical science and associated regulatory components of client projects and providing mentoring and coaching to more junior analytical staff.You keep up to date with the latest technical advances in analytical science and, where appropriate, introduce those technologies into the business.

If successful, you will be expected to support the growth of the business by providing technical consultancy and advice to the company's clients, scientific guidance to internal staff and support to business development activities.Typical responsibilities/accountabilities:

  • Bring analytical expertise to guide the development of fit for purpose analytical methods for a range of simple and complex drug products, and trouble shoot any method development issues.
  • Understand and articulate global regulatory requirements for a CMC submission and design the product strategy accordingly.
  • Ensure the company has the right analytical expertise and capability to support existing and new client programmes, including the introduction of new analytical technologies as appropriate
  • Provide hands on laboratory trouble shooting for complex analytical challenges when required.
  • Act as pharmaceutical development project leader / manager for some client projects
  • Manage and review CRO activities on behalf of clients
  • Management of the financial and contractual aspects of projects with clients, such as costing proposals and invoicing.
  • Act as a key point of contact for the company's global client base.
  • Participate and present at network events, conferences

Education, Qualifications, Experience, Skills and Capabilities:

  • Educated to PhD and greater than 5 years' experience in the pharmaceutical sciences and drug development or bachelor's degree and greater than 10 years' experience in the pharmaceutical sciences and drug development
  • Experience of progressing the analytical components of various drug projects through different development phases (discovery to launch) across global markets
  • Wide ranging experience of interactions with global regulatory authorities
  • Good understanding of ICH quality guidelines and global CMC regulatory requirements

If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV to Selby at Selby. For more information regarding this position or any others, please call Selby on .

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit www.srg.co.uk to view our other vacancies.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.