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Expired
  • Location: Sandwich
  • Salary: Up to £23 per hour (£35K salary equivalent)
  • Job Type:Contract

Posted over 1 year ago

  • Sector: Scientific Development, Quality
  • Contact: Tunde Olashore
  • Contact Email: tunde.olashore@nextphaserecruitment.com
  • Contact Phone: 01403 216216
  • Duration: 18.0 MONTH
  • Start Date: 2022-07-27
  • Job Ref: V-47427

Are you looking to take your analytical skills to the next level? Do you have some experience of working in a solid dose pharmaceutical environment? Do you have some experience working in a regulated analytical laboratory setting with a strong background inHPLC and GC?

This is an exciting opportunity to join a global pharmaceutical organisation, working as an Analytical Scientist. You will support the application of chromatography methods to understand impurities in a broad range of excipients and active pharmaceutical ingredients.

The role is an 18-month contract and it’s based in Sandwich, Kent. There is a competitive hourly rate ranging from £17 to £23, working through an umbrella company.


SKILLS NEEDED:

  • Proven experience with the application of chromatography methods to quantify impurities

  • Demonstrated application of wider suite of analytical methods to build understanding of material attributes.

  • Understanding of analytical approaches to evaluate elemental impurities

  • Ability to work independently, and to present analytical results and conclusions.

  • Excellent communication and interpersonal skills, both written and verbal are required.

  • Design, follow and review protocols, scientific methods, and departmental procedures.

  • Experience with HPLC/UPLC method development & validation

    • Strong written and oral communication skills.

    • Independent, accountable, attention to detail, ability to effectively balance multiple projects, and strong interpersonal/communication skills are required.

    • Must be highly motivated and self-directed

    • Demonstrates good interpersonal skills and works well with personnel at all levels.


 ROLE RESPONSIBILITIES:

  • Support the development and application of chromatography methods for the quantitation of small molecule impurities.

  • Evaluate chemical properties of a broad range of excipients using suite of analytical methods.

  • Determine the elemental chemical profiles of APIs, excipients and drug products to enable understanding of composition and impurities to support product investigations and process understanding.

  • Perform experiments in accordance with good laboratory practices (GLP), established business processes and protocols, and applicable SOPs.

  • Document laboratory work that is detailed, timely and in compliance with GLP requirements

  • Conduct technical data reviews, and present data interpretation and conclusions to customers for making informed decisions.

  • Prepares and reviews technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.