What are the responsibilities and job description for the Validation Engineer position at Tranzeal Incorporated?
Job Title: Validation Engineer
Location: Phillipsburg, NJ (Onsite)
Schedule: Monday–Friday, 8-Hour Shift
About the role:
We are seeking a Quality Engineer with experience supporting quality systems and compliance activities within pharmaceutical, biotech, or chemical manufacturing environments.
Required Qualifications:
• 5 years of Quality Assurance/Quality Engineering experience
• GMP investigations and CAPA management
• Root Cause Analysis and Change Control processes
• Customer Complaint Investigations
• Internal Audits and ISO 9001 compliance
• Validation support experience
• Experience in pharmaceutical, biotechnology, or chemical manufacturing
Preferred Education:
• BS in Chemistry, Biology, Biochemistry, Microbiology, or Chemical Engineering
Key Responsibilities:
• Lead quality system and continuous improvement initiatives
• Manage customer complaint investigations and CAPA activities
• Support GMP, regulatory, customer, and internal audits
• Ensure compliance with cGMP and ISO requirements
• Participate in validation activities and process improvements
• Collaborate with cross-functional teams to resolve quality issues
If you have a strong background in regulated manufacturing environments and quality systems, we'd like to connect.