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Hovione
Quality Control AssociateHovione • lisboa, distrito de lisboa, Portugal
Quality Control Associate

Quality Control Associate

Hovione • lisboa, distrito de lisboa, Portugal
Há 7 dias
Descrição do cargo

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.

  • Apply and develop QC knowledge while participating in procedures and projects under guidance from senior staff.
  • Ensure all tasks comply with GMP, quality standards, and legal regulations, escalating issues when needed.
  • Plan and execute method development, transfer, validation, and reporting activities accurately and on time.
  • Resolve analytical issues collaboratively and escalate unresolved problems per defined procedures.
  • Maintain clear, proactive communication with internal and external stakeholders, representing the team when required.
  • Propose new methodologies and suggest optimizations to improve processes and performance.
  • Support onboarding of new team members and ensure high professional standards across the lab.
  • Maintain laboratory records, logbooks, and data systems in accordance with GLP and internal procedures.
  • Conduct instrument maintenance, calibration, and qualification, while adhering to HSE and GMP guidelines.
  • Work effectively in cross-functional teams, support audits, and contribute to KPI tracking and continuous improvement initiatives.
  • Use analytical techniques and instrumentation, such as gas and high-performance liquid chromatography (HPLC) amongst others.

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).
  • Requires educational / training experience in a QC laboratory environment.
  • Hands-on experience in Analytical Chemistry and QC procedures (desirable).
  • Training and experience of GMP and ICH guidelines standards (desirable).
  • Knowledge on HPLC and GC, and familiarity with Empower Software (desirable).
  • Technical understanding of GMP practices, analytical theory and techniques.
  • Documentation skills and attention to detail - Fluency in English is a requirement.
  • 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 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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Quality Control Associate • lisboa, distrito de lisboa, Portugal

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