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Research Scientist/ Technical Specialist

Employer
Thornshaw Recruitment
Location
Westmeath, Leinster (IE)
Salary
Negotiable depending on experience
Start date
23 Sep 2020
Closing date
23 Oct 2020

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Discipline
Quality, GMP, QC Analyst
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

My client, a global CRO company based in the midlands, is recruiting for Technical Specialist/ Associate Research Scientist to join their team.

This role is a senior level Technical Specialist role. The role of the ARS is to act as a Subject matter expert, lead scientific projects and provide full analytical testing support in accordance with GMP practices, including analytical method development, validation and transfer. This is an exciting opportunity to join a Lab that focuses on method development, validation, transfer, stability and quality control testing for all phases of drug development. 

Key Responsibilities:

  • Co-ordinate all aspects of managing method development and validation
  • Supervise and assist senior technical staff in laboratory operations
  • Interface with clients on scientific issues, study design and project technical requirements
  • Plan, direct and implement improvements in systems and processes in order to enhance efficiency and quality
  • Assist with strategic planning, business development and new technology implementation

Skills and experience:

The successful candidate will possess a Degree (or equivalent) in Chemistry. Significant industry experience within an analytical testing laboratory and GMP environment is essential, as well as solid scientific supervisory experience in the pharmaceutical or analytical contract laboratory industry (to include R&D project and program management, direct supervision of technical staff, and direction of laboratory operations).

This person should be an SME with HPLC, Dissolution, Physicals testing (Foreign Particulates, KF, Particle Size Distribution, etc).

Other requirements also include: 

  • 6-8 years of solid experience in GMP regulated Laboratory environment.
  • Expertise in GMP regulated environment in the areas of analytical method development, validation and transfer for a variety of dosage forms, using a variety of instrumentation which may include (but not limited to) the following:  HPLC, Dissolution, HIAC, KF, Zetasizer, Mastersizer, and other applicable analytical instruments.
  • Extensive knowledge with Foreign Particulate tests & Particle Size Distribution tests, as well as extensive knowledge of all the Physicals Testing techniques.
  • Excellent analytical expertise in method development, validation and transfer
  • Excellent communication and presentation skills
  • Excellent technical writing skills
  • Excellent ownership skills for Laboratory Investigations and Deviations
  • Strong technical mentoring and training skills
  • Ability to build and develop client relationships
  • Understanding of budgeting and revenue projection
  • Ability to plan, organize and work to deadlines

For more information and to apply for this role please call Zoe on +353 1 2784671 or e-mail zhamilton@thornshaw.com

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. Www.thornshaw.com Tel: +353 1 2784671

Company

thornshaw-title

Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission

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For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com

 

Company info
Website

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