AstraZeneca

Senior Engineer, Automation Controls - Facilities & Engineering

AstraZeneca$132K — $199K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, preferably Electrical Engineering; Master's degree preferred.
  • 7-10 years of experience in automation/controls systems, qualification/validation, and facilities engineering, preferably in pharmaceuticals.
  • Extensive knowledge of GMP, FDA regulations, and compliance requirements.
  • Experience leading complex automation processes, engineering projects, and capital investments.
  • Strong project management skills, including budgeting and scheduling.
  • Excellent analytical, problem-solving, and communication skills.
  • Ability to manage multiple priorities and work effectively under pressure.

Responsibilities

  • Lead and guide technical teams in automation controls and engineering solutions.
  • Mentor junior engineers and foster cross-functional support for automated systems.
  • Oversee the maintenance and operation of automation/control systems across facilities.
  • Develop and implement strategies to improve automation/control systems.
  • Lead validation strategies and ensure compliance with regulatory requirements.
  • Manage capital projects related to automation/control systems.
  • Prepare, review, and ensure compliance of project documentation.

Benefits

  • 401(k) retirement program with contributions.
  • Paid vacation and holidays.
  • Health benefits including medical, dental, and vision coverage.
  • Paid leaves for various circumstances.
Full Job Description
Introduction to role

The Senior Engineer, Automation Controls - Facilities & Engineering is responsible for leading and managing the technical aspects of facilities and process automation/controls, including development and validation, engineering projects, and capital investments within a pharmaceutical organization. This role involves providing expert technical guidance, overseeing complex projects, and ensuring that all systems and processes meet regulatory requirements and support operational efficiency.

Accountabilities

Leadership and Oversight:

  • Lead technical teams and provide guidance on facilities and process automation/controls, including development and validation activities, engineering solutions, and capital projects.


  • Mentor and support junior engineers and other technical staff in development of cross functional support for automated systems.


  • Collaborate with cross-functional teams to align engineering and project activities with organizational goals.


Facilities Management:

  • As asset owner, oversee the maintenance and operation of automation/control systems and equipment within the site including critical facilities/utilities, laboratories, production areas, and administrative spaces.


  • Develop and implement strategies for facility automation/controls improvements and upgrades to enhance operational efficiency and compliance.


  • Ensure automation/controls systems adhere to health, safety, and environmental regulations.


Validation Management:

  • Lead the development and execution of validation strategies, protocols, and documentation for site systems, equipment, and processes with focus on assets associated with automation/controls.


  • Ensure that validation activities meet regulatory requirements (e.g., FDA, EMA) and internal standards.


  • Manage complex validation projects, including protocol design, execution, and reporting.


Automation/ Controls Oversight:

  • Oversee automation/controls programs to ensure the reliability of systems including electrical components, software environments, and automated field devices.


  • Develop and implement maintenance and inspection programs for critical equipment.


  • Ensure automation/controls engineering procedures and processes comply with industry standards and regulatory requirements.


Engineering Leadership:

  • Lead engineering projects related to the design, installation, and commissioning of systems and equipment.


  • Ensure engineering activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations.


  • Develop and implement preventive and predictive maintenance programs to enhance equipment reliability.


Capital Projects Management:

  • Manage all aspects of capital projects, including automation/controls systems upgrades, expansions, and new installations.


  • 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.


Documentation and Reporting:

  • Prepare and review comprehensive documentation for qualification/validation, engineering procedures and work instructions, and capital projects.


  • Generate detailed reports on project status, validation results, project activities, and asset ownership/maintenance work.


  • Ensure that documentation is accurate, complete, and compliant with regulatory requirements.


Compliance and Safety:

  • Ensure all facilities, systems, and processes comply with regulatory requirements and industry standards.


  • Develop and enforce safety protocols and emergency response plans.


  • Conduct regular audits and inspections to ensure compliance and address any issues promptly.


Continuous Improvement:

  • Identify and implement process improvements to enhance efficiency, reduce costs, and improve system reliability.


  • Stay current with industry trends, technological advancements, company guidance, and regulatory changes to ensure best practices are applied.


Essential Skills/Experience

  • Bachelor's degree in Engineering, Electrical Engineering preferred, or a related engineering field; Master's degree preferred.


  • 7-10 years of experience in automation/controls software and equipment systems, with background in qualification/validation, facilities engineering, and capital projects. Significant experience in a pharmaceutical or regulated industry is preferred.


  • Extensive knowledge of GMP, FDA regulations, and other relevant compliance requirements.


  • Proven experience in leading complex automation/controls processes, asset ownership, 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.


Desirable Skills/Experience
  • Cell Therapy Experience


The annual base pay for this position ranges from $$132,900 - $199,351. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions 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.

Date Posted
01-Jul-2026

Closing Date
23-Jul-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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