Sr Res Assoc II vacancy at Gilead in Foster City

Gilead is in need of Sr Res Assoc II on Thu, 21 Mar 2013 04:28:28 GMT. Independently plans and executes experiments that support method validation and method transfer actives. Writes method validation and method transfer protocols and reports. Writes and revises methods, specifications, and SOPs as needed. Lead/coordinate QC and cross-functional projects with limited direction. Is able to identify, effectively communicate and troubleshoot complicated issues...

Sr Res Assoc II

Location: Foster City California

Description: Gilead is in need of Sr Res Assoc II right now, this vacancy will be placed in California. For complete informations about this vacancy opportunity kindly read the description below. Independently plans and executes experiments that support method validation and method transfer actives. Writes method validation and method transfer protocols and reports. Writes and revises methods, specifications, ! and SOPs as needed. Lead/coordinate QC and cross-functional projects with limited direction. Is able to identify, effectively communicate and troubleshoot complicated issues. Proactively seeks out senior personnel to discuss potential solutions to problems. Is able to clearly present results of work, interpret data and draw conclusions. May act as a resource as needed in other areas in QC. Demonstrates and applies advanced level of understanding of ICH guidance with regards to method validation planning. Participates and presents updates at group meetings.

Essential Duties and Job Functions:

  • Conducts routine analyses based on written procedures
  • Reviews data and results of testing to ensure compliance to appropriate specifications and protocols.
  • Performs maintenance and calibration of analytical instrumentation.
  • Begins to learn and apply knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Pract! ices (GLPs) on a daily basis.
  • Writes simple protocols! and reports.
  • Must have working knowledge of Microsoft Office software.
  • Participates in group meetings. May present data or prepare information for others to present.
  • Conduct non-routine analysis of raw materials, intermediates, and finished product samples.
  • Troubleshoot instrumentation and test methods.
  • Assists in the training of QC staff as needed.
  • Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory
  • Working knowledge and proficiency with Microsoft Office software.
  • Writes and executes protocols and reports.
  • Evaluates equipment for purchase and performs installations and qualifications of the new instruments.
  • Troubleshoot instrumentation/test methods. Lead/coordinate QC and cross-functional projects with limited direction.
  • Leads the training of QC staff.
  • Independently plans and executes assigned experiments that support routine develo! pment activities and project goals.
  • Writes and revises methods, specifications, and SOP’s as needed.
Knowledge, Experience and Skills:
  • 5+ years of experience with BS degree in a relevant scientific discipline.
  • 3+ years of experience with MS degree in a relevant scientific discipline.

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If you were eligible to this vacancy, please email us your resume, with salary requirements and a resume to Gilead.

If you interested on this vacancy just click on the Apply button, you will be redirected to the official website

This vacancy starts available on: Thu, 21 Mar 2013 04:28:28 GMT



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