About Hovione
At Hovione, we help partners turn scientific innovation into medicines that reach patients around the world. For more than 65 years, we have connected science, technology, and manufacturing to scale complex ideas into high-quality and innovative solutions that truly make a difference.
As an international Contract Development and Manufacturing Organization (CDMO), we support the development and manufacture of drug substances, intermediates, and drug products across the full life cycle. We are globally recognized for our leadership in specialized technologies such as Spray Drying and Continuous Tableting. But what truly sets us apart is not just what we do — it is how we do it: with purpose, care, collaboration, and a deep commitment to doing the right things right.
Our people are the reason for our success. We are a global and diverse team of more than 2,600 team members across Europe, the USA, and Asia, bringing together different experiences and perspectives to help our partners to overcome complex challenges. We believe that an inclusive environment — where everyone, regardless of background, identity or ability, is respected, heard and empowered to contribute — is essential to drive innovation, ensure quality, and secure long‑term sustainable success.
And as we grow, so do the opportunities for our people to develop, broaden their perspectives, and build meaningful careers. Because at Hovione, better starts with those who choose to make a difference every day. Will you be one of them?
You will be responsible to:Define and implement Quality Control (QC) techniques to ensure the quality of raw materials, intermediates, finished products, and analytical services in compliance with GMP, regulatory requirements, and client specifications.Execute, manage, and support analytical projects, ensuring timely, safe, compliant, and cost-effective delivery.Perform and coordinate analytical activities including:- Method development
- Method creation and transfer
- Method validation
- Protocol preparation
- Report preparation
- Bachelor's degree (or equivalent) in:
- Chemistry
- Chemical Engineering
- Pharmaceutical Sciences
- Biochemistry
- Health Sciences
- Related scientific discipline
- Experience or training within a Quality Control laboratory environment.
- Hands-on experience in Analytical Chemistry and QC activities preferred.
- Experience with method development, validation, and transfer is advantageous.
- Working knowledge of GMP and ICH guidelines is desirable.
- Knowledge of analytical techniques including:
- HPLC
- GC
- Other chromatographic and analytical methodologies
- Familiarity with Empower software is preferred.
- Strong understanding of analytical chemistry principles, laboratory practices, and GMP requirements.
- Experience with laboratory information management systems and electronic documentation.
- Strong attention to detail and documentation skills.
- Excellent organizational and problem-solving abilities.
- Ability to work effectively in cross-functional teams.
- Strong communication and stakeholder management skills.
- Proactive mindset with a continuous improvement approach.
- Commitment to quality, compliance, and safety.
- Fluency in English.
- Proficiency in Microsoft Office applications.
- Ability to work in accordance with GMP, HSE, and regulatory standards
Hovione is a proud Equal Opportunity Employer
Inclusion and diversity are key to us. We are committed to creating an inclusive recruitment experience and welcome applications from all qualified candidates. If you require any reasonable accommodation or support during the application or interview process, please contact us, and we will be happy to assist.
Notice to Agencies and Search Firms Representatives
Hovione does not accept unsolicited resumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral.
Skills Required
- Bachelor's degree or equivalent in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Health Sciences, or a related scientific discipline
- Experience or training within a Quality Control laboratory environment
- Hands-on experience in analytical chemistry and QC activities
- Experience with method development, validation, and transfer
- Working knowledge of GMP and ICH guidelines
- Knowledge of HPLC, GC, and other chromatographic or analytical methodologies
- Familiarity with Empower software
- Understanding of analytical chemistry principles, laboratory practices, and GMP requirements
- Experience with laboratory information management systems and electronic documentation
- Fluency in English
- Proficiency in Microsoft Office applications
- Ability to work in accordance with GMP, HSE, and regulatory standards
What We Do
Hovione is an international company with over 60 years of experience in pharmaceutical development and manufacturing operations. As a Contract Development and Manufacturing Organization (CDMO) with a fully integrated offering of services for drug substances, drug product intermediates and drug products. The company has four FDA inspected sites in the USA, Portugal, Ireland and China and development laboratories in Lisbon, Portugal and New Jersey, USA. Hovione provides pharmaceutical customers services for the development and compliant manufacture of innovative drugs, including highly potent compounds, and customized product solutions across the entire drug life cycle. In the inhalation area, Hovione offers a complete range of services, from API, formulation development and devices. Hovione´s culture is based on innovation, quality and dependability. Hovione was the first Chemical/ Pharmaceutical Company to become a Certified B Corp, is a member of Rx-360, EFCG and participates actively in industry quality improvement initiatives to lead new global industry standards.
