Principal Method Development Scientist

Principal Method Development Scientist

Biotechnology Clinical Life Sciences

Location Adelaide, Australia

Salary £50,000 - £65,000

Contract Permanent

Reference HMAUPMDSc

Date Posted

Consultant

Apply now

6 weeks left to apply


We have an exciting opportunity for a highly experienced Principal Method Development Scientist at a leading CRO based in Australia. The ideal candidate will have proven experience in LCMS/MS assay development for NCEs, with working knowledge in a regulated, GLP bioanalytical laboratory.

Key Responsibilities and Duties:

  • Perform Principal Method Development Scientist duties in the LCMS bioanalytical lab
  • Develop, transfer and pre-validate assessments of assays and analytical methods to support drug analysis
  • Provide technical expertise on troubleshooting and technical investigations of analytical methods
  • Design LCMS/MS protocols for drug optimisation, method development and the processing of analytical runs
  • Liaise with clients (external) and SDs (internal) on project status and timelines, including on-site visits; perform audits when required
  • Author and/or review of Analytical Laboratory Methods (ALMs)
  • Review and manage new projects as required
  • Prepare and review bioanalytical reports
  • Provide leadership and supervision, as well as training of R&D staff
  • Contribute to the Continuous Improvement

Ideal Skills and Qualifications:

  • Degree qualified, or equivalent, in a relevant scientific discipline
  • 5-10 years’ experience in LCMS/MS development in a regulated bioanalytical and Assay Development laboratory
  • Proven GLP and CRO experience; required
  • Demonstrated Study Director/Principal Investigator experience; required
  • Previous experience in communicating with clients on high level science issues as well as remaining strictly confidential
  • Ability to mentor, train and supervise
  • Ability to work effectively both in isolation and as part of a team
  • Ability to analyse problems, formulate effective solutions and coordinate tasks simultaneously

The company is a Contract Research Organisation specialising in providing drug development services for the pharmaceutical and biotechnology industries. You will be working in their state-of-the-art facilities based in Adelaide, Australia with Visa and relocation support provided.

If you are interested or have any questions about this role, feel free to contact Harriet at CY Partners.

Tagged as: , , , , , , , , , ,


Principal Method Development Scientist

Biotechnology Clinical Life Sciences

Apply now

6 weeks left to apply

Quick Apply

Already a member?

Yes, send me relevant communications
I accept the terms and conditions and privacy policy of CY Partners.


Related Vacancies

QC Specialist

Life Sciences Pharmaceuticals

Location

ContractContract

An exciting opportunity has arisen for a number of QC Specialists to join a world leading pharmaceutical company, based at their site in Maidenhead. As a QC Specialist you will be responsible…

Lab Analyst

Chemical Life Sciences Pharmaceuticals

LocationMaidenhead

Salary£11.54 per hour

ContractTemporary

Lab Analyst An opportunity has arisen for a number of Lab Analysts to join a world leading pharmaceutical company. Based at their site in Maidenhead on an initial 6-month period, this could be…

Project Manager – Drug Development

Biotechnology Clinical Pharmaceuticals

LocationOxford

SalaryUp to £30,000

ContractPermanent

Project Manager – Drug Development An exciting position for an experienced drug development project manager to join a biotechnology start-up company. The role of Project Manager is a critical role in successfully…