Project Engineer, Validation Engineer

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Glendale, CA, US

30+ days ago Requisition

Salary Range: $90,000.00 To $ Annually

ELIQUENT Life Sciences is a leading global consulting group delivering regulatory affairs, pharmacovigilance, quality, and compliance solutions that support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.

ELIQUENT Life Sciences is a trusted global consulting firm helping life sciences companies navigate regulatory complexity and bring breakthrough therapies to market. Founded by former regulators and industry experts, we offer end-to-end support in regulatory affairs, pharmacovigilance, and quality compliance. Our team is driven by a shared mission to improve global health through innovation, collaboration, and integrity. At ELIQUENT , you will be part of a purpose-led organization where your expertise contributes to meaningful impact and your growth is supported every step of the way.

As a Project Engineer specializing in Pharmaceutical Engineering within the manufacturing sector, you will play a critical role in supporting the design, development, and commissioning of pharmaceutical manufacturing processes and equipment. Your primary objective will be to ensure that all engineering solutions meet regulatory standards and operational efficiency requirements, facilitating the successful production of high-quality pharmaceutical products. You will collaborate closely with cross-functional teams including quality assurance, production, and project management to implement best practices and troubleshoot technical challenges.

This role demands a proactive approach to commissioning activities, ensuring that new systems and equipment are validated and fully operational according to project timelines. Ultimately, your contributions will help optimize manufacturing workflows, enhance compliance, and support the company’s commitment to delivering safe and effective pharmaceutical products to market.

• Bachelor’s degree in Pharmaceutical Engineering, Chemical Engineering, or a related engineering discipline.
• Demonstrated experience in pharmaceutical manufacturing environments, specifically in commissioning and validation activities.
• Strong understanding of regulatory requirements such as FDA, cGMP, and other relevant industry standards.
• Proficiency in interpreting engineering drawings, specifications, and technical documentation.
• Excellent communication and teamwork skills to effectively collaborate with multidisciplinary teams.

• Advanced degree or certifications related to pharmaceutical engineering or manufacturing.
• Experience with automation systems and control technologies used in pharmaceutical production.
• Familiarity with project management methodologies and tools.
• Knowledge of risk management and quality assurance processes within pharmaceutical manufacturing.
• Previous consulting experience in a pharmaceutical or biotech environment.

• Lead and support commissioning activities for pharmaceutical manufacturing equipment and systems, ensuring compliance with industry regulations and company standards.
• Collaborate with engineering, quality, and production teams to develop and implement process improvements and validation protocols.
• Conduct technical assessments and provide recommendations to optimize manufacturing processes and equipment performance.
• Prepare and review technical documentation, including commissioning plans,…