Senior C&Q Validation Engineer – GMP Analytical & Process Equipment- (JP15147)
3 Key ConsultingThousand Oaks, California, United States
Posted March 31, 2026
130000 - 140000 USD
Full Time
About the Company
3 Key Consulting is a specialized staffing and consulting firm with 12 years of experience placing business and IT professionals in the life sciences and healthcare sectors. Leveraging a broad network of industry experts and partnerships with leading academic institutions, the firm offers a full suite of talent acquisition services—including PEO, compliance, and niche domain staffing in biomedical, pharma, medical devices, and business intelligence. Its core focus on people, process, and technology enables faster, cost‑effective solutions that improve workforce productivity and market efficiencies. 3 Key’s collaborative culture and commitment to delivering better, faster, and more efficient staffing and consulting services distinguish it as a trusted partner for organizations seeking high‑quality talent and operational excellence.
Job Description
The Senior C&Q Validation Engineer will lead and/or execute commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities for a leading global biopharmaceutical company. Key skills include experience in commissioning/qualification/validation, knowledge of cGMP commissioning/qualification/validation practices, and experience working with cross-functional stakeholders.
Requirements
- Demonstrable experience in a pharmaceutical, biotech, or life science organization in a C&Q/CQV role
- Knowledge of quality assurance principles
- Experience working within project teams and multiple projects in parallel
- Effective communication skills, both verbal and written
- Able to think analytically with the ability to resolve issues
- Able to manage own time efficiently
- Experience with Kneat Gx Platform or other digital C&Q systems