QUALITY ASSURANCE SITE MANAGER

The HOUSE OF ABY Group brings together 10 brands within a single ecosystem, covering a wide range of sectors such as aerospace, digital technologies, nuclear, pharmaceuticals, railways, and infrastructure. This diversity makes HOUSE OF ABY a true environment for professional growth, offering its consultants and Business Partners the opportunity to develop their careers across different industries, roles, and projects while continuously taking on new challenges. Thanks to this multi-brand organization, everyone can build a tailored career path, develop their skills, explore new fields, and work on high value-added projects. ABYLSEN is the engineering consulting company of the HOUSE OF ABY Group, supporting its clients in the implementation of technological projects through highly qualified consultants. Its mission is to deliver expertise, innovation, and execution capability. For more than 20 years, Abylsen has established itself as one of the leading engineering consulting companies in Europe, supporting over 660 clients in their industrial, digital, and operational projects. Our areas of expertise:

• Research & Development (R&D)
• Production & Operations
• Digital & IT
• Industrialization
• Validation & Testing
• Maintenance & Safety

As part of the growth of Abylsen Italy, specializing in Transportation (Automotive, Aeronautics, Defence, Space, and Railway), Heavy Industry (Metallurgy and Steelmaking), Energy, and IT, we are looking for a Quality Assurance Site Manager for a leading client operating in the Pharma sector. What will be your challenge? You will join a long-term international project within the pharmaceutical industry, playing a key role in Quality Assurance activities in highly regulated and structured environments. Your responsibilities will include the handling of deviations, non-conformities, CAPAs, and change controls, as well as supporting documentation review processes and quality-related activities across the organization. Working closely with multidisciplinary teams and international stakeholders, you will contribute to maintaining high-quality standards while driving continuous improvement initiatives. Technical Skills:

• Master’s degree in Pharmacy, Chemistry, Biotechnology, Biology, Pharmaceutical Sciences, or a related scientific discipline.
• At least 5 years of experience in Quality Assurance within the pharmaceutical industry.
• Strong understanding of quality systems and quality-related processes within regulated pharmaceutical environments.
• Experience managing deviations, non-conformities, CAPAs, and change controls.
• Ability to manage quality documentation and interact effectively with cross-functional teams.

Soft Skills:

• Excellent command of English (minimum C1 level).
• Candidates must have the legal right to work within the European Union.

Additional Information:

• Location: Copenhagen, Denmark.
• Long-term international project within the pharmaceutical industry.
• On-site position with a standard Monday-to-Friday working schedule.
• Employees have the opportunity to return to their home country every four weeks.

What We Offer:

• Permanent Italian employment contract.
• Annual gross salary (RAL) between €35,000 and €40,000, depending on experience and in accordance with Italian employment regulations.
• Daily allowance of €125 for the entire duration of the international assignment.
• Additional breakfast allowance of €15 per day.
• Accommodation fully covered by the company.
• Company car available for both business and personal use.
• Fuel expenses fully covered by the company.

No barrier should stand in the way of talent! Committed to equal opportunities, our Group embraces an inclusive approach: every position is open to everyone, and we actively support the integration of people with disabilities. This vacancy is open to all genders, in accordance with Italian Laws No. 903/77 and No. 125/91, as well as to candidates of all ages and nationalities, in accordance with Legislative Decrees No. 215/03 and No. 216/03.