Job Description
This role is for an individual who can work independently or as part of a team, communicating with transparency and demonstrating respectful behavior at all times. The ideal candidate will be able to gather and organize information, meet commitments on scope and time, and follow directions to perform well-defined tasks effectively.
Responsibilities
* Generate, execute, and review master and completed qualification and validation protocols, summary reports, and associated data for conformance to regulations, SOPs, specifications, and other applicable acceptance criteria.
* Analyze the results of testing and determine the acceptability of results against pre-determined criteria.
* Investigate and troubleshoot problems that occur and determine solutions or recommendations for changes and/or improvements.
* Review, edit, and approve deviation notifications, deviation investigations, and corrective actions.
* Review and approve change controls, SOPs, reports, and other documentation.
* Coordinate with other departments or outside contractors/vendors to complete validation tasks.
Requirements
* A BS/BA in Engineering, Chemistry, or Life Science.
* Associate Level: 0-2 years of experience; Specialist Level: 3+ years of experience directly related to the field.
Benefits
The company offers comprehensive benefits, which may include health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels. The company is an equal opportunity employer and provides reasonable accommodation to known disabilities or chronic illnesses of an otherwise qualified applicant for employment.
About Us
We have an inclusive and diverse culture that values respect, communication, and teamwork. If you are a motivated and detail-oriented individual who is passionate about delivering high-quality results, we encourage you to apply for this exciting opportunity.