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?
Oversee and supervise all production activities to ensure efficient, safe, and right‑first‑time operations aligned with cGMP, HSE, and business requirements;
Promote a strong safety and quality culture by identifying risks, implementing mitigation actions, and ensuring compliance with all regulations and standards;
Drive continuous improvement by proposing and implementing optimizations in processes, equipment, procedures, and team performance;
Lead and develop the production team through coaching, training, workload allocation, performance feedback, and support for career and talent development;
Ensure operational excellence by coordinating production schedules, managing equipment readiness, supervising sampling processes, and responding effectively to deviations or equipment downtime;
Oversee accurate completion, maintenance, and revision of production documentation, including production records, protocols, indicators, and system entries (e.g., SAP, LIMS, SchedulePro);
Maintain a clean, organized, and compliant facility while ensuring proper use of PPE, equipment calibration, and resolution of nonconformities;
Support audits, investigations, and hazard assessments, and foster open communication by proactively reporting issues and proposing solutions;
Facilitate regular team communication through meetings and briefings, maintaining alignment with KPIs, objectives, and organizational policies;
Perform any additional duties required for safe, compliant, and effective production operations, ensuring adherence to all GMP, HSE, and corporate procedures.
Full secondary education (mandatory), supported by a science or engineering qualification or equivalent practical experience.
Mandatory experience in manufacturing/production environments, with formal knowledge of process systems used in fine chemicals or pharmaceutical operations.
Significant experience specifically in fine chemicals or pharmaceutical production, with Senior Production Operator training considered highly desirable.
Strong understanding of ChemOps and PharmOps unit operations, combined with very strong knowledge of GMP regulations.
Proven ability to coordinate others in operational environments and perform tasks defined in the technical competences matrix.
Basic numerical capability and strong written and verbal communication skills; English proficiency highly desirable.
Computer literate and knowledgeable of area management practices, including 5S, management indicators, waste management rules, safety standards, and continuous improvement systems.
Possesses the required knowledge, experience, and skills to perform tasks in line with established procedures and operational requirements.
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 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.
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