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Go to next pageKatalyst Healthcares and Life Sciences
Katalyst Healthcares and Life Sciences - St Joseph
Work at Katalyst Healthcares and Life Sciences
Responsibilities: - Validation documentation Authoring (validation plans, user requirements specifications, risk assessment, IQ-OQ-PQ protocols, trace matrix and summary reports).
- Experience in validating GMP Lab systems and Equipment.
- Responsible for assuring a system/application meets its requirements as outlined in system specification (URS/FRS) per process defined in the Validation Plan for the project.
- Identify and escalate, as necessary project risks and issues to the CSVC Manager.
- Engage in multiple CSVC projects through the assimilation of data, establishing facts and drawing valid conclusions to deliver results in accordance with resources, constraints and business needs.
- Be able to prepare reports on defects and problems that arise during system testing.
- Have solid oral and written communication skills and teamwork skills.
- Be a good team player, able to meet deadlines and handle changing priorities.
- Have strong judgment capabilities to clarify requirements when necessary.
- Have the ability to work with cross functional teams.
- Have solid experience working with validated systems.
- Work with business representatives to ensure the test cases reflect business rules and processes.
- Fulfills a subject matter expert role(s) for critical quality and compliance GxP end-use applications supporting Animal Health business processes.
Requirements: - GMP/Regulated lab, more than 5 years of CSV experience required.
- Technical writing Experience.
- Highly skilled in Computerized System testing and validation in the healthcare industry.
- Knowledge of GxP regulations (e.g. 21 CFR Part 11, Annex 11).
- Solid project organizational skills. Ability to multi-task.
- Must have strong analytical problem-solving skills.
- Excellent communication including written, verbal, and listening skills.
- Self-motivated, detail oriented, takes initiative and ability to work independently without close supervision.
- BS in Science or Technical Writing Degree.
See details and apply
Sr. Computer system Validation Engineer
