Qualifications

• Bachelor's Degree in STEM field required; Biomedical or Chemical Engineering preferred
• 1-3+ years of experience in CQV, validation, or related roles
• Hands-on experience with IQ/OQ protocols and commissioning activities
• Familiarity with GMP/GDP documentation processes
• Proficient in reading P&IDs and technical documentation
• Strong organizational and problem-solving skills
• Ability to work independently in fast-paced settings

Responsibilities

• Execute IQ/OQ protocols to ensure compliance and functionality
• Perform detailed walkdowns and verification of engineering systems
• Support change management and field verification aligned with engineering documentation
• Assist in temperature mapping and process validation activities
• Document and resolve non-conformances and discrepancies
• Maintain accurate compliance documentation within a cross-functional team
• Collaborate with various departments to ensure operational readiness

Benefits

• High growth potential in a fast-paced, people-focused environment
• Performance-based incentive programs alongside competitive pay
• Comprehensive company-paid insurance options including life and disability
• Medical, dental, and vision coverage available
• 401(k) with employer matching
• Paid Time Off with rollover options and additional sick leave
• Tuition reimbursement to support ongoing education
• Team social activities fostering a fun workplace culture
• Recognition programs to celebrate employee contributions