Job Description
Seeking a mid- to senior-level Validation Engineer to support commissioning and qualification activities within a pharmaceutical manufacturing environment. The role will be responsible for generating and executing IQ, OQ, and PQ protocols for equipment, utilities, and packaging systems, ensuring compliance with cGMP and regulatory expectations. The candidate should be comfortable working both independently and collaboratively, with the ability to lead validation activities and drive projects to completion.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin...