Validation Engineer

Join to apply for the Validation Engineer role at PharmEng Technology

Join to apply for the Validation Engineer role at PharmEng Technology

About The Job Validation Engineer

About The Job Validation Engineer

Job Title : Validation Engineer Lyophilization Specialist

Location : Sanford, NC (Long-Term Contract)

About the Role : We are seeking an experienced Validation Engineer specializing in lyophilization processes and equipment. The ideal candidate will lead validation activities, ensuring compliance with regulatory standards while supporting manufacturing excellence in a pharmaceutical or biotech setting.

Key Responsibilities

• Develop and execute validation protocols for lyophilization equipment and processes.
• Perform Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for lyophilizers.
• Create, review, and maintain validation documentation, including protocols, reports, and risk assessments.
• Conduct validation testing to meet regulatory and industry compliance standards.
• Collaborate with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing.
• Address validation issues and implement corrective and preventive actions (CAPA).
• Stay updated on industry trends and regulatory changes related to lyophilization and validation.
• Participate in audits concerning validation processes.
• Provide training and guidance on validation protocols and best practices.

Qualifications

Preferred Skills

Apply Now : If you are a detail-oriented Validation Engineer with expertise in lyophilization, we encourage you to apply and contribute to cutting-edge pharmaceutical advancements. This is a unique opportunity to work on impactful projects in a dynamic and innovative environment.

Seniority level

Seniority level

Mid-Senior level

Employment type

Employment type

Full-time

Job function

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing

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