What are the responsibilities and job description for the Validation Engineer position at iS CLINICAL?
Embark on an extraordinary journey with us at Innovative Skincare, home of the renowned iS CLINICAL cosmeceutical brand. We are not just about creating groundbreaking skincare products; we are about creating chemistry that extends beyond the lab – a dynamic synergy between our products and our people.
At Innovative Skincare, we believe in a unique formula: the perfect blend of professional expertise and cultural harmony. This philosophy fuels our brand’s continuous growth and empowers each member of our team. We are more than a company; we are a community bound by passion, dedication, and a deep love for what we do, crafting an atmosphere that is as vibrant and energizing as our products.
Who we are: Discover a world where skincare innovation meets scientific excellence at Innovative Skincare, a globally acclaimed leader in high-performance cosmeceuticals. Our journey is rooted in the relentless pursuit of creating skincare products that are not only effective but transformative. At the heart of our brand is the iS CLINICAL line, renowned for its fusion of nature’s finest ingredients with cutting-edge science. We are driven by a deep understanding of skin biology and a passion for unlocking the secrets of skin health and rejuvenation.
Our ethos is built on the pillars of innovation, integrity, and excellence. Our team members at Innovative Skincare are part of a company that is shaping the future of skincare, where your work contributes to the well-being and confidence of people globally. Join us and be a part of this exciting alchemy where your talent meets our vision, creating a world of pure chemistry!
About the role: The Validation Engineer is responsible for developing, executing, and documenting validation protocols to ensure equipment, systems, and processes meet regulatory and company requirements. This role supports GMP compliance by validating new and existing equipment, utilities, and manufacturing processes.
This position will be on-site in our new Mesa, AZ facility.
Duties/Responsibilities:
- Develop and execute validation protocols (IQ, OQ, PQ) for equipment, utilities, and processes.
- Prepare and maintain validation documentation, reports, and records.
- Ensure compliance with GMP, SOPs, and regulatory guidelines.
- Support commissioning and qualification of new equipment and systems.
- Investigate and resolve validation deviations or non-conformances.
- Work with Quality, Engineering, and Production teams to implement validated systems.
- Participate in risk assessments and change control activities.
- Support audits, inspections, and continuous improvement in validation practices.
- Train staff on validation procedures when required.
Education and Experience:
- Bachelor’s degree in Engineering, Life Sciences, or related field required.
- 2 years of experience in validation, quality, or engineering in a GMP-regulated industry.
- Strong knowledge of validation principles, protocols, and regulatory standards (FDA, cGMP, ISO).
- Experience with equipment qualification and process validation preferred.
- Strong organizational, analytical, and documentation skills.
- Good communication and cross-functional teamwork abilities.
- Must be able to lift up to 40 lbs and work in lab, production, and utility environments.
Physical Requirements:
- Must be able to stand and walk for extended periods of time
- Must be able to sit and use a computer for long periods of time
Our company is dedicated to providing equal employment opportunities and embraces diversity and inclusion in our workplace. All eligible candidates will be considered for employment without bias towards their race, ethnicity, religion, gender, gender identity or expression, sexual orientation, national origin, genetic information, disability, age, or veteran status.
Benefits: 401k, Life, Dental, Vision, Health, PTO