Employment Opportunities

Analytical Chemist

Dated: January 11, 2012

Validation Resources is looking for an experienced analytical chemist to join a team of dedicated scientists who are engaged in studies to identify trace unknowns extracted from polymeric materials.

Position responsibilities include: sample preparation and sample analysis using various analytical instruments governed by controlled procedures/methods; data analysis; interpreting results; writing reports and coordinating studies with laboratory resources. Position also includes the maintenance, troubleshooting and repair of analytical instruments. The ideal candidate is a self-manager and a team player who can thrive in an FDA-regulated environment where practices are governed by cGMP. Key skills include problem-solving, precise analytical technique, good laboratory hygiene, excellent communication abilities, technical writing and accurate data handling.

Requirements:

  • Education: BS in chemistry (with focus on analytical techniques)
  • Experience: Minimum two years relevant industry experience including:
  • Hands-on experience with Agilent 6890/7890-5975 GC-MS and/or Agilent 1100/1200-SL series HPLC-UV-MS performing sample analysis, data analysis and instrument maintenance/troubleshooting.
  • Background working in a regulated laboratory (FDA cGMP or GLP preferred).

Employment Details:

  • Position: Full-time with benefits
  • Location: Bend, Oregon
  • Compensation: Competitive and dependent on experience and qualifications.
  • Potential Start Date: Feb 2012
  • Principals only. Recruiters, please don't contact this job poster.
  • Please no phone calls about this opening.
  • Qualified Candidates: please submit cover letter and current CV to info@validation-resources.com.

Quality System Manager

Dated: October 3, 2011

Validation Resources is looking for a Quality Systems Manager. The Quality Systems Manager will be responsible for maintaining and enhancing the Quality System of an FDA regulated laboratory providing analytical services to the pharmaceutical industry. Responsibilities include all facets of Quality System management including but not limited to: CAPA program; internal/external audits; training program; equipment qualification; calibration and preventive maintenance program; document control; quality records maintenance and Part 11 compliance. The position includes responsibility for the evaluation of processes leading to the accurate and reliable generation of data for a drug or biologic product; defining and implementing quality metrics; and providing ongoing training for employees in Quality System compliance.

The qualified candidate must have experience managing a Quality System in a GMP, GLP and/or relevant ISO laboratory environment supporting the pharmaceutical industry and be experienced in the applicability of Part 11 requirements to a contract analytical laboratory. The qualified candidate must also have analytical instrument experience including hands on use of HPLC-UV, GC-MS, LC-MS, FTIR, and/or UV-Vis systems as well as data analysis and interpretation. Experience with USP test methods is desired. Ability to work well with a team is a requirement for success.

  • Education/Experience: Bachelor degree or higher in analytical chemistry or related field with minimum five years of experience in a controlled laboratory environment.
  • Position: Full-time with benefits
  • Location: Bend, Oregon
  • Compensation: Competitive and dependent on experience and qualifications.
  • Potential Start Date: Feb/Mar 2012
  • Principals only. Recruiters, please don't contact this job poster.
  • Please no phone calls about this opening.
  • Submit cover letter and CV toinfo@validation-resources.com.