Application and Validation Scientist
$63,400–$120,000 year
On-siteBurlington, Massachusetts, United States
Job Summary
Execute IQ/OQ validation protocols for microbiological testing equipment at customer sites, installing supplies, performing tests, documenting results, and writing reports. Train customers on equipment operation and provide PQ consulting for test method suitability. Troubleshoot on-site equipment issues and assist with calibration and preventive maintenance. Coordinate with customers and internal functions to complete validations while partnering with sales to support opportunities. Prepare weekly and monthly reports, manage workloads, and develop testing protocols. Requires 50-70% travel.
Required Qualifications
- Bachelor's Degree in Chemical Engineering, Biomedical Engineering, Chemistry, Biology, or other Engineering or Life Science discipline
- 1+ years lab experience in the pharmaceutical industry
- Must be eligible to work in the US
- This position requires 50-70% travel
Desired Qualifications
- Ability to develop and execute IQ/OQ validation protocols
- Extremely proficient planning and organizational ability, able to coordinate work schedule on short notice
- Comprehensive knowledge of cGMP regulations and documentation requirements
- Strong analytical and problem-solving skills
- Effective writing and verbal communication skills
- Ability to be a team player/work well alone and with others
- Ability to multi-task
- Customer-focused
- Agile, flexible and adaptable
- Proactive/action oriented
- Well developed customer-facing skills
- May lead small projects with limited risks and resource requirements
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