Engineer – Facilities and Engineering

Engineer - Facilities and Engineering

Are you ready to engineer reliability at scale so life-changing medicines reach patients without delay? Join a team that turns robust engineering, smart investment, and disciplined execution into secure, efficient, and compliant production across a global network.

In this role, you will combine project leadership, GMP expertise, and a Lean mindset to lift performance across critical assets and facilities. From shaping maintenance strategies and capital renewals to resolving deviations, you will reduce downtime, strengthen compliance, and unlock capacity that supports product launches and stable supply in fast-moving markets.

This role will be based in Tarzana, CA.

Key Responsibilities

• Engage with cross functional technical teams and provide input on facilities maintenance, validation activities, metrology practices, engineering solutions, and capital projects.
• Work with senior engineers and technical staff and support major engineering initiatives via projects and standard work.
• Collaborate regularly with multiple departments to align engineering and project activities with organizational goals.

• Oversee assigned segments of the maintenance and operation of facilities, including laboratories, manufacturing areas, and ancillary GMP spaces.
• Support development and implementation of strategies for facility improvements and upgrades to enhance operational efficiency and compliance.
• Ensure facilities adhere to health, safety, and environmental regulations.

• Support the development and execution of validation strategies, protocols, and documentation for systems, equipment, and processes.
• Ensure that validation activities meet regulatory requirements (e.g., FDA, EMA) and internal standards.
• Manage mid-size validation projects, including protocol design, execution, and reporting.

• Support metrology programs by ensuring the accuracy and reliability of measurement systems and instruments.
• Develop and implement calibration, maintenance, and inspection programs for critical equipment.
• Review and revise metrology practices to ensure compliance with industry standards and regulatory requirements.

• Lead mid-size corrective maintenance/engineering projects related to the design, installation, and commissioning of new or modified systems and equipment.
• Ensure engineering activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations.
• Develop and implement preventive maintenance programs to enhance equipment reliability. Support predictive maintenance initiatives led my senior team members.

• Manage aspects of capital projects, including facility upgrades, expansions, and new construction, with minimal support from senior team members.
• Develop project plans, budgets, and schedules; monitor progress and ensure projects are completed on time and within budget.
• Coordinate with internal stakeholders, external contractors, and vendors to achieve project objectives and compliance.

• Prepare and review comprehensive documentation for validation, metrology, engineering, and capital projects.
• Generate detailed reports on project status, validation results, calibration activities, and maintenance work.
• Ensure that documentation is accurate, complete, and compliant with regulatory requirements.

• Ensure all facilities, systems, and processes comply with regulatory requirements and industry standards.
• Develop and enforce safety protocols and emergency response plans.
• Conduct routine audits and area inspections to ensure compliance and address any issues promptly.

• Identify and implement process improvements to enhance efficiency, reduce costs, and improve system reliability.
• Stay current with industry trends, technological advancements, and regulatory changes to ensure best practices are applied.

Minimum Qualifications:

• Bachelor’s degree in Engineering, Facilities Management, or a related field; Master’s degree.
• 4 years of experience in facilities, validation, metrology, engineering, and capital projects, with significant experience in a pharmaceutical or regulated industry.
• Extensive knowledge of GMP, FDA regulations, and other relevant compliance requirements.
• Proven experience in leading mid-size validation processes, asset management, metrology programs, facilities, engineering projects, and capital investments.

Desirable:

• Strong project management skills with experience in budgeting, scheduling, and resource allocation.
• Excellent analytical, problem-solving, and communication skills.
• Ability to manage multiple priorities and work effectively under pressure.

The annual base pay for this position ranges from  $101,643.20 - $152,464.80 USD Annual. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.  Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.