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Hovione

CDMO for complex drug APIs manufacturing

Assembly Engineering Manager

Engineering LeadershipPosted on Nov 5
Full-timeLoures, PortugalNo salary listedIn-person

About the Job

Requirements

  • A degree in Engineering—Mechanical, Electrical, Electronic, Instrumentation, Civil, or a related field—is mandatory.
  • A proven track record in industrial engineering or maintenance environments is required; experience in pharmaceutical, chemical, or food and beverage industries is preferred.
  • Demonstrated experience leading and developing engineering teams in project or operational contexts is required.
  • Solid knowledge of cGMP, HSE practices, and applicable regulatory requirements, including FDA and EMEA, is strongly desirable.
  • Familiarity with ICH, ISPE, and ISO guidelines applicable to pharmaceutical technical installations is required.
  • Strong leadership and the ability to inspire, develop, and hold teams accountable are required.
  • A solid command of engineering principles, technical regulations, and industry standards is required.
  • The candidate must be fluent in English.
  • Proficiency in MS Office is required.

Responsibilities

  • Lead assembly, commissioning, and qualification activities for facilities, utility systems, and process equipment at the Sete Casas site, and oversee assigned capital projects from early design through GMP-compliant handover.
  • Work cross-functionally with Process, Quality, HSE, and Automation to deliver projects on time, on budget, and to cGMP standards.
  • Lead, coach, and develop team members, including recruitment, onboarding, training, and performance management in line with company HR policies.
  • Translate business objectives into departmental and individual goals, ensuring team alignment and accountability; foster engagement and motivation.
  • Conduct performance reviews, define individual development plans, manage underperformance with HR, and support succession planning and career progression.
  • Plan, manage, and execute engineering and maintenance activities following asset lifecycle management principles.
  • Develop and implement annual master plans covering budgets, resource allocation, and success metrics; deliver area KPIs, monitor performance, and drive corrective actions and continuous improvement.
  • Manage outsourced contractors and service providers to meet site quality, safety, and schedule requirements; report project progress, pending items, and deadlines weekly and escalate relevant deviations.
  • Lead assembly, commissioning, and qualification phases (DQ/IQ/OQ/PQ) for assigned capital projects.
  • Incorporate cGMP and HSE requirements into URS and design specifications from early project phases; develop installation plans showing criticality, dependencies, and milestones.
  • Identify and implement technical solutions to construction and commissioning challenges without compromising design intent or process functionality.
  • Participate in, issue, review, and approve commissioning and qualification documentation, including protocols, test datasheets, instrument impact assessments, and reports.
  • Coordinate commissioning and qualification with Design Engineering, Automation, QC, QAU, and user areas; lead external qualification contractors and optimize their time and cost.
  • Ensure facilities are handed over fully commissioned and qualified, meeting user requirements and cGMP guidelines; maintain punch lists with accountable owners and deadlines while ensuring cGMP and HSE compliance.
  • Ensure equipment and processes comply with applicable local, national, and industry regulations, including FDA, EMEA, ICH, ISPE, and ISO, and ensure adherence to GMP requirements and internal standards including SOPs, COPs, and HBR.
  • Promote and maintain an EHS culture across engineering activities and teams.
  • Execute change control assessments, obtain authorization before scope changes or additional work, investigate deviations, and implement CAPAs.
  • Define technical competency requirements for the team and implement structured training plans.
  • Participate in client and health authority audits within Qualification and Validation.
  • Own and monitor departmental budgets, track deviations, and implement corrective actions; optimize internal and external resource allocation to meet operational, project, and financial targets.
  • Ensure assigned tasks are planned and delivered on time, safely, efficiently, and cost-effectively.

Desired Qualifications

  • Experience in pharmaceutical, chemical, or food and beverage industries is preferred.
  • Experience with capital project management, including planning, cost control, and reporting, is valued.
  • Knowledge of project management tools and CAD software is a plus.
  • Portuguese language skills are an advantage.

About the Company

Hovione

CDMO for complex drug APIs manufacturing

Hovione is a contract development and manufacturing organization that creates and scales active pharmaceutical ingredients (APIs) for medicines. It handles complex chemistry and specializes in processes like particle engineering and spray drying to improve drug absorption. It differentiates itself through a long history of tackling difficult compounds, deep manufacturing expertise, and an FDA-inspected global footprint across Portugal, Ireland, China, and the US. Its goal is to help drug developers bring new medicines to market efficiently by providing high-quality, scalable manufacturing and expanding capacity, especially in the U.S.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Loures, Portugal
Founded
1959

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