Join a Market Leader:
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::
Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.
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Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements.
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Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.
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Prepare and implement changes to QC procedures and analytical methods, ensuring proper approvals.
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Issue, track, and follow up on change controls and CAPA-related events within required timelines.
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Ensure proper functioning, maintenance, calibration, and qualification of lab instruments and reference standards.
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Maintain and improve lab information systems; prepare and review QC documentation, protocols, and reports in compliance with cGMP and HSEE.
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Request quotations and manage stock control for instruments, materials, and reagents to ensure lab operations.
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Lead/conduct and participate in root-cause investigations, document findings, and support closure of OOS/OOT incidents and QC deviations.
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Apply investigation tools in analytical investigations (internal or cross functional investigations).
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Define CAPAS aligned with the root-cause determination.
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Support internal and external audits and assist in compiling audit responses related to QC. Perform tasks safely and efficiently, monitor risks, and ensure adherence to HSE and GMP standards.
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Apply and expand QC knowledge in instrumentation, stability, and deviation handling under senior guidance.
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Deliver assigned tasks reliably, on time, and cost-effectively, while complying with company policies and procedures.
We are looking to recruit a Candidate::
- University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field (mandatory)
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Typically requires 3-5 years of relevant experience in a QC laboratory environment, preferably under pharmaceutical cGMP (desired)
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Training and experience of GMP and ICH standards (mandatory)
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Experience of HSE rules and regulations (mandatory)
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Experience of investigational analysis (desired)
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Strong understanding and knowledge of GMP and ICH practices, analytical theory, and techniques
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Knowledge of EU/US quality related pharmaceutical regulations
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Competence in conducting quality-based investigations and root cause analysis
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Fluency in English is a requirement
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Computer literate with good working knowledge of the MS Office package
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.
