Instrument Connectivity and Qualification Engineer (Consultant)
About The Position
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Requirements
- Experience with LabVantage
- Experience with URS, IQ, OQ, IVI documentation
- Experience with instrument qualification
- Experience with CSV deliverables
Responsibilities
- Develop and maintain a tracking log (e.g., Excel, Smartsheet) of site-specific documentation required to enable instrument connectivity for all instruments in scope for LabVantage (e.g., URS, IQ, OQ, IVI, and related deliverables).
- Complete LabVantage instrument registration in accordance with site procedures and project standards.
- Provide additional support, as required and commensurate with experience, to prepare and/or execute instrument qualification and/or CSV deliverables.
Benefits
- Diversity, equity, and inclusion initiatives
- Opportunity to unleash innovative, collaborative, and entrepreneurial spirits
- Safe space where all employees feel empowered to succeed
- Personalized application review by a recruitment team member
- Outcome provided for all applications
- Support for remote working
- Encouragement for hybrid work model for those near offices
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
501-1,000 employees
