QC Associate

Join a Market Leader

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

Propose and implement new analytical methodologies based on project requirements.Troubleshoot analytical issues, conduct investigations, and escalate complex problems when required.Review and verify analytical data, documentation, and work generated by the team to ensure compliance with procedures and quality standards.Investigate deviations, incidents, and CAPAs (Corrective and Preventive Actions).Act as a liaison between QC, internal stakeholders, clients, and cross-functional teams.Support onboarding, training, and development of new team members.Perform equipment maintenance, calibration, and qualification activities.Maintain laboratory records, notebooks, logbooks, and electronic systems in accordance with GLP and GMP requirements.Accurately utilize laboratory information systems and analytical software.Conduct analytical testing using techniques such as HPLC, GC, and other laboratory instrumentation.Interpret analytical results and ensure accurate documentation and data integrity.Contribute to continuous improvement initiatives, KPI reporting, audits, inspections, and regulatory investigations.Promote a strong culture of quality, compliance, safety, and operational excellence.Ensure compliance with all GMP, HSE, company procedures, and regulatory requirements.

We are looking to recruit a Candidate:

Education

• Bachelor's degree (or equivalent) in:
  • Chemistry
  • Chemical Engineering
  • Pharmaceutical Sciences
  • Biochemistry
  • Health Sciences
  • Related scientific discipline

Experience

• 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.

Technical Skills

• 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.

Competencies

• 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.

Additional Requirements

• 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.