Zifo is working with a large pharma client to build a team of laboratory IT (lab computing, Lab IT systems, QA, Validation) professionals. This role will require a 100% on-site presence in Albany, NY.
Requirements
Responsibilities:
· Support life cycle documents and execution
· Author validation life cycle documents for client review and approval
· Route drafted documents for review
Request approval workflows to Doc Control
· Route reviewed documents for workflow approval
· Request performance copies for protocols
· Execute approved protocols
Qualifications:
- Bachelor’s/ Master’s degree or equivalent in a scientific or health care field.
- 2-5 years experience as a Technical Consultant, preferably in the pharmaceutical /Life sciences industry preferred.
A successful Zifo-ite is:
- Independent, Self-Motivated & Results driven
- Willing & able to quickly acquire new Technical Skills & Business Principles
- A critical thinker who possesses logical reasoning
- Curious and always looking for creative solutions to complex problems
Benefits
About Zifo:
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we deb...
Zifo
Zifo is a global scientific informatics service provider working across research, development, manufacturing, and clinical domains.
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