Scientist I Immunoassay- New Grad (ELISA needed) at Alliance Pharma
Fordham, England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

26 Aug, 25

Salary

26000.0

Posted On

27 May, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Hospital/Health Care

Description

Responsibilities

  • Development & validation of Immunoassay methods for quantitation of drugs & biomarkers.
  • Be familiar with and work in accordance with, SOP’s and Study Documents.
  • Applocation of these methods to routine analysis of samples from pre-clinical toxicology and clinical safety studies.
  • Record keeping in compliance with GLP.
  • Be able to accurately communicate the outcomes of your experiments
  • Make suggestions for how processes can be improved
  • Take an interest in your own personal development, seek out training, and look for opportunities to grow
  • Embrace the Laboratory Charter, keeping your work areas clean and tidy and being respectful to your colleagues
  • Be flexible and productive; realise that timelines, priorities and requirements will change regularly and respond to these challenges positively.
  • Be familiar with, and work to the Resolian Health and Safety Policy relevant to your role, paying particular attention to COSHH in the lab.
  • Complete any mandatory training appropriate for your role.

Education, Skills & Experience

  • Degree in biological science, or equivalent relevant experience (essential)
  • Excellent attention to detail (essential)
  • Experience in a GXP accredited laboratory (desirable)
  • Familiarity with ELISA techniques (essential)
  • Ability to communicate effectively to peers and customers (essential)

Job Type: Full-time
Pay: £24,000.00-£26,000.00 per year

Schedule:

  • Monday to Friday

Work Location: In perso

How To Apply:

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Responsibilities
  • Development & validation of Immunoassay methods for quantitation of drugs & biomarkers.
  • Be familiar with and work in accordance with, SOP’s and Study Documents.
  • Applocation of these methods to routine analysis of samples from pre-clinical toxicology and clinical safety studies.
  • Record keeping in compliance with GLP.
  • Be able to accurately communicate the outcomes of your experiments
  • Make suggestions for how processes can be improved
  • Take an interest in your own personal development, seek out training, and look for opportunities to grow
  • Embrace the Laboratory Charter, keeping your work areas clean and tidy and being respectful to your colleagues
  • Be flexible and productive; realise that timelines, priorities and requirements will change regularly and respond to these challenges positively.
  • Be familiar with, and work to the Resolian Health and Safety Policy relevant to your role, paying particular attention to COSHH in the lab.
  • Complete any mandatory training appropriate for your role
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