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HPLC Analyst

HPLC Analyst

Russell Taylor

Posted 19 hours ago, valid for 5 days

Cambridge, Cambridgeshire CB2 8AG, England

Full Time

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Sonic Summary

The role of HPLC Analyst is available in Cambridgeshire with a competitive salary based on experience and additional benefits including 25 days of holiday and a flexible working schedule.
Russell-Taylor Group is seeking both junior and senior analytical chemists with experience in LCMS or HPLC, although GMP experience is not mandatory.
Candidates should have a degree in a scientific subject and previous experience in pharmaceutical manufacturing is desirable, along with HPLC method validation and development skills.
Responsibilities include performing analytical techniques, developing and validating methods, and ensuring compliance with safety regulations and good laboratory practices.
The position offers training for junior candidates, making it an excellent opportunity for those looking to advance their careers in pharmaceutical analysis.

Role: -HPLC AnalystLocation: -CambridgeshireSalary & Benefits: -Competitive Salary (DOE), 25 days holiday plus benefits, flexible working schedule, company pension, cycle to work scheme & onsite parking.Russell- Taylor Group have multiple opportunities for Analytical Chemists to join our Pharmaceutical Analysis client in Cambridgeshire.Our client is recruiting for a number of junior and senior analysts with experience in LCMS or HPLC, GMP is not essential for this role.Roles are available for people who already have method validation and development experience, but also more junior candidates can apply as you will be trained and developed in this area.Responsibilities• Perform analytical techniques such as HPLC and LCMS- Develop, validate and implement analytical methods.• Conduct analysis on pharmaceutical products. • Follow specified methods and help to write up reports. • Communicate with clients for standard requests, but with support of the team manager.• Ensure compliance with safety regulations and good laboratory practices (GLP)• Keep accurate records of laboratory results and updating SOPs as needed.The Person• Educated to degree level or equivalent in Scientific subject.• Previous Pharmaceutical Manufacturing experience (GMP) • HPLC experience- method validation & method development would be valuable.• Experience in the analysis pharmaceutical products (desirable)• Experience of method development and validation would be advantageous.• Experience working to GLP or GMP • Previous experience of problem solving and working in a fast-paced environment.Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.

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