Validation Engineer - Pharmaceutical Sterile Manufacturing

Nivagen Pharmaceuticals • Sacramento, CA

11d • $90,000 - $105,000 • Onsite

About The Position

At Nivagen as a Validation Engineer you will be responsible for ensuring that manufacturing processes, equipment, utilities, and systems in the sterile pharmaceutical production environment meet all regulatory requirements, industry standards, and company specifications.
The role involves independently working and supporting the validation lifecycle from installation through qualification and routine re-validation activities, ensuring that the company's sterile manufacturing processes are in compliance with cGMP (current Good Manufacturing Practices) and other regulatory guidelines such as FDA, EMA, and ISO standards.

Requirements

• Bachelor's degree or Diploma in Pharmaceuticals, or a related field.
• Minimum 2 years of experience in a pharmaceutical manufacturing or validation role, with a focus on sterile manufacturing (e.g., aseptic processing, sterile filling, isolator, autoclave sterilization).
• Strong understanding of cGMP, FDA, EMA, ISO standards, and other relevant regulatory requirements.
• Experience with equipment validation (e.g., filling machines, autoclaves, and HVAC systems) and process validation.
• Familiarity with the documentation requirements for validation, including protocol development, execution, and report writing
• Excellent technical writing and documentation skills.
• Strong attention to detail and ability to manage complex technical documentation.
• Ability to work cross-functionally and manage multiple priorities.
• Familiarity with data analysis tools and software used for validation testing and reporting (e.g., Excel, Validation Master Plans, LIMS systems).
• Aseptic processing or sterile manufacturing practices.
• Must live or willing to move to Sacramento Metropolitan Region (Approx. 40 miles’ radius)
• Willing to travel as needed basis to other manufacturing sites for vendor support

Responsibilities

• Perform or oversee the Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of new and existing equipment and systems.
• Qualification of equipment in sterile manufacturing facility (e.g., aseptic processing, sterile filling, isolators, autoclave sterilization).
• Ensure compliance with regulatory requirements for equipment qualification and validation.
• Knowledge of validation equipment like Kaye validator, temperature and RH data loggers etc.
• Prepare and review validation reports to ensure they meet regulatory and company requirements.
• Maintain traceability of validation activities and ensure all validation records are accurately documented, maintained, and stored.
• Conduct and manage process validation studies to confirm the sterility and quality of pharmaceutical products.
• Work with cross-functional teams (e.g., production, quality control, engineering) to optimize manufacturing processes and ensure consistency and repeatability.
• Support the development and implementation of new processes, ensuring that they are validated per regulatory requirements.
• Knowledge of cleaning validation will be an added advantage
• Perform any additional tasks as assigned by the Validations Lead

Benefits

• $90,000 to $105,000
• Yearly bonus eligibility
• Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being
• Medical, dental and vision coverage
• Paid time off plan
• 401k savings plan

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 11-50 employees