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 and technology 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:- Organize daily priorities and execute sample analyses accurately and on time to meet laboratory plans and KPI targets;
- Adhere to laboratory testing schedules to ensure an efficient and effective Quality Control system;
- Generate, review, and maintain analytical data in full compliance with GMP, HSE, operating procedures, and industry standards;
- Maintain laboratory records, checklists, and notebooks to GMP standards and in accordance with internal procedures;
- Ensure high standards of laboratory hygiene, housekeeping, and overall QC laboratory compliance;
- Perform routine calibration, preventive and corrective maintenance of laboratory equipment, and manage required consumables and spare parts;
- Identify, report, and support the investigation of deviations, OOS/OOT/atypical results, non-conformances, and QC incidents;
- Communicate effectively with internal departments and support audits using established processes and IT systems;
- Proactively seek information, undertake additional tasks as required, and complete all performance review requirements;
- Conduct all activities safely and in compliance with GMP, legal, environmental, health, and safety regulations, while promoting Hovione processes and good practices.
- Master's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Health Sciences, or a related scientific discipline;
- Relevant work experience;
- Proven practical pharmaceutical or related industry experience in a GMP regulated environment;
- Hands-on experience in Analytical Chemistry and quality control testing methodologies;
- Strong knowledge of GMP, GLP, ICH guidelines, and pharmaceutical quality systems;
- Ability and availability to work in shift patterns, as required by business needs;
- Strong analytical thinking, problem-solving capabilities, and attention to detail;
- Fluency in English, both written and spoken;
- Proficiency in MS Office applications and excellent technical documentation skills.
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 RepresentativesHovione does not accept unsolicited résumes 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. Thank you for your understanding.
Skills Required
- Master's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Health Sciences, or a related scientific discipline
- Relevant work experience
- Practical pharmaceutical or related industry experience in a GMP-regulated environment
- Hands-on experience in analytical chemistry and quality control testing methodologies
- Strong knowledge of GMP, GLP, ICH guidelines, and pharmaceutical quality systems
- Ability and availability to work assigned shift patterns
- Strong analytical thinking, problem-solving capabilities, and attention to detail
- Fluency in written and spoken English
- Proficiency in Microsoft Office applications
- Excellent technical documentation skills
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.
