AstraZeneca

Engineer, Facilities and Engineering

AstraZeneca$101K — $152K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Facilities Management, or related field; Master's preferred.
  • 4-6 years of experience in facilities, validation, metrology, engineering, and capital projects within a pharmaceutical setting.
  • In-depth knowledge of GMP, FDA regulations, and compliance standards.
  • Experience leading mid-size validation processes and managing capital projects.
  • Strong project management skills with budgeting and scheduling experience.
  • Excellent analytical and communication abilities.
  • Ability to manage multiple priorities in a high-pressure environment.

Responsibilities

  • Lead cross-functional teams for facilities maintenance and capital projects.
  • Oversee operations in labs and GMP spaces to ensure compliance and improvements.
  • Develop validation strategies and documentation for FDA compliance.
  • Manage metrology programs to ensure measurement accuracy and compliance.
  • Direct maintenance and engineering projects following GMP standards.
  • Manage capital projects from planning to execution.
  • Generate project status reports and ensure documentation accuracy.
  • Conduct audits and enforce safety protocols to comply with regulations.

Benefits

  • Qualified retirement programs.
  • Paid time off including vacation, holidays, and leaves.
  • Health, dental, and vision coverage as per plan terms.
  • Short-term incentive bonuses for performance.
  • Equity-based awards for eligible roles.
Full Job Description
Job Summary:

The Engineer - Facilities & Engineering is responsible for various technical aspects of facilities maintenance, validation activities, engineering projects, and mid-size capital investments within a pharmaceutical organization. This role involves providing technical input, overseeing facility and engineering related projects, and ensuring that all systems and processes meet regulatory requirements and support operational efficiency.

Key Responsibilities:
  • Lead cross-functional teams supporting facilities maintenance, validation, metrology, engineering solutions, and capital projects.
  • Oversee facilities operations across labs, manufacturing, and GMP spaces, driving improvements while ensuring health, safety, environmental, and regulatory compliance.
  • Lead validation strategies, protocols, and documentation for systems and equipment, ensuring compliance with FDA/EMA requirements.
  • Oversee metrology programs, including calibration, inspection, and measurement system accuracy, while maintaining industry compliance.
  • Lead corrective maintenance, engineering projects, and preventive/predictive maintenance initiatives in accordance with GMP requirements.
  • Manage capital projects (upgrades, expansions, and new installations), including planning, budgets, schedules, and execution.
  • Prepare and review validation, metrology, engineering, and capital project documentation and generate project status reports.
  • Conduct audits, enforce safety protocols, and ensure compliance with regulatory and quality standards.
  • Drive continuous improvement initiatives to enhance efficiency, reliability, and cost-effectiveness while staying current with industry and regulatory trends.

Qualifications:
  • Bachelor's degree in Engineering, Facilities Management, or a related field; Master's degree preferred.
  • 4-6 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.
  • 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.

Working Conditions:
  • Office and on-site facilities environment, with occasional travel to various company sites or off-site locations.
  • May require occasional evening or weekend work to address urgent issues or project needs.


The annual base pay for this position ranges from $101,643.20 - $152,464.80. 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.

Date Posted
09-Aug-2026

Closing Date
30-Aug-2026

About AstraZeneca

AstraZeneca is a British-Swedish multinational pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs. The company was formed in 1999 through the merger of Astra AB and Zeneca Group plc. AstraZeneca's products are used to treat a wide range of medical conditions, including cancer, cardiovascular disease, respiratory disease, and diabetes. The company has operations in over 100 countries and employs more than 76,000 people worldwide. AstraZeneca is committed to developing innovative medicines that improve the health and well-being of people around the world.
Learn more about AstraZeneca
Size
83,100 employees
Market Cap
$211.5 billion
Industry
Net Income
$3.1 billion
Founded
1999
5 Year Trend
+10.2%
Revenue
$26.6 billion
NASDAQ

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