Validation Specialist III

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Job Title: Validation Specialist III

Location: Framingham, MA

Duration: 8 Months (Possible Extension)

Job Responsibilities:

• Perform validation (IQ, OQ, PQ) of various types of equipment and systems including validation or requalification of temperature controlled chambers and lab equipment.

• This would include refrigerators, cold rooms, freezers, incubators, liquid N2, etc.

• Write and execute validation protocols and write validation reports including thorough resolution of protocol deviations or non-conformances.

• Investigate/troubleshoot validation problems or issues; conduct statistical analysis of testing results.

• Perform 21 CFR Part 11 and EU Annex 11 gap assessment on existing scientific application software that is being used in laboratories. Develop 21 CFR Part 11 and EU Annex 11 compliance plan.

• Assess compatibility of instrument software with existing windows operating system.

• Collaborate with instrument software vendors to execute 21 CFR Part 11 and EU Annex 11 compliance plan including preparation of user requirement specifications (URS) and functional specifications, GxP impact assessment, risk assessment and validation (IQ/OQ/PQ).

• Receive instructions on related assignments under general supervision.

• The position will report to Manager, Quality Process Analysis with a dotted line to the Manager, R&D Validation.

Qualifications

Qualification:

• Experience or familiarity with applicable US and worldwide regulatory requirements for the biotechnology industry (EU Annex 11, 21CFR Part 11, etc.).

• Demonstrated knowledge of GMP regulations and good documentation practices is required.

• Familiarity with application software such as Waters MassLynx, Beckman-Coulter 32 Karat, Applied Biosystems 7500 SDS, Molecular Devices Softmax Pro, Gage InSite, TrackWise, etc.

• Proficiency with MS Word, MS Excel, MS Access, MS PowerPoint, MS Project.

• Experience with Microsoft Word, Excel, Project, and Visio.

Additional Information

All your information will be kept confidential according to EEO guidelines.