ALK-Abelló A/S

Automation Engineer

Are you looking for an exciting opportunity to develop your manufacturing skills in a growing, international pharmaceutical company? At ALK, we are on a mission to improve the lives of people living with allergies, and we are seeking a dedicated and driven Automation Specialist to join our Automation Department. 

 

Your key responsibilities:

Automation Specialist supports all production activities regarding automated processes, systems and equipment on-site to ensure work is performed and ensures compliance with corporate requirements and site policies. Key responsibilities include:

  • Provide support to the areas associated with qualified systems.
  • Lead changes related to qualifications when modifications affect the qualified status of equipment or systems.
  • Perform initial qualifications of computerized equipment and systems. 
  • Ensure qualified status is maintained through periodic reviews according to evaluated frequency. 
  • Provide support in handling deviations, especially those impacting the qualified status of equipment in production and utilities areas.
  • Manages the scope, deliverables, schedule, budget and quality of engineering projects related to cGMP production equipment and systems.
  • Manages the design, implementation, and qualification of automation systems.
  • Maintains company reputation by enforcing compliance with local, state and federal regulations.
  • Work closely with global IT teams to ensure adherence to corporate cybersecurity policies and global system design standards.
  • Prepares and develops User Requirement Specifications for automated equipment, software, and systems. 
  • Supports QA/validations through preparation of design documents and protocol review. 
  • Recommends and manages implementation of appropriate corrective/preventative actions for existing equipment and manufacturing processes. 
  • Experience on Automation Systems and processes; involved in different phase of Definition, deployment, integration or qualifications: 
  • Development of projects of Automation, Control and Instrumentation (PLCs, sensors etc). 
  • Lean Manufacturing and Historical data Systems (KPIs). 
  • Software Management and Support for production equipment, vision systems, labelling, and Packaging. 
  • Evaluates, approves, prepares and executes change control documentation and validation documentation. 
  • Acts as Subject Matter Expert during regulatory inspections. 
  • Maintains clean and safe working environment by enforcing SHE policies and procedures. 
  • Maintains company reputation by enforcing compliance with local, state and federal regulation.

 

Your profile:

  • Education: Degree in Engineering, Electronics and industrial automation, or related technical field.
  • Experience: Minimum 5 years in pharmaceutical engineering or validation roles.
  • Proven ability to understand and follow written and verbal instructions in English.
  • Knowledge of GMP and qualification principles.
  • Knowledge in production OT systems and IT architectures. 
  • Experience with systems, utilities and production equipment. 
  • Demonstrate proficiency with industry project management practices and tools. 
  • Strong documentation and organizational skills. 
  • Ability to lead technical changes and manage cross-functional communication. 
  • Ability to analyze data and make conclusions based on the data 
  • Able to work in a team across departments and sites 
  • Clear understanding of other team members roles and responsibilities 
  • Ability to represent the department or organization in local and global projects with assistance from other cross functional team members.  
  • Identifies opportunities for improvement and makes constructive suggestions for change to improve both project management and/or process effectiveness.  
  • Demonstrate initiative and good interpersonal skills, able to work in a team. 
  • Ability to work with Quality Systems and regulatory requirements such as:  CFRs, GMP, FDA, OSHA. 
  • Demonstrated ability to comply with required safety practices. 
  • Understanding of validation principles and applications for computer systems, equipment and PLC’s. 

We provide:

  • Competitive salary package.
  • Career development opportunities and continuous trainings.
  • Stable employment and a positive work environment.
  • A comprehensive benefits package including health insurance, subsidized meals, and a pension plan.

 

If you’re excited about building a better future in health, ALK is the right place for your ambitions.

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Region:

  • Comunidad de Madrid

Job type:

Permanent

Working hours:

Full-time

Working days:

Day

Industry sector:

Maintenance/Technical support

Job level:

Employee

Position type:

Engineer

Application deadline:

30/09/2026

Location:

Madrid, Spain

Company homepage:

http://www.alk.net

Office address:

Calle Miguel Fleta 19, 28037 Madrid

Office location: