Analyst

UNAVAILABLE; Loures; Presencial; EUR 23 000 - 32 000; Tempo integral

Resumo da oferta

Hovione, a leading CDMO, is seeking a QC Laboratory professional to verify drug product quality and oversee analytical testing within GMP-compliant workflows.

The role requires a mandatory high school diploma and a chemistry-related qualification, plus GMP QC lab experience and strong communication in English. Shifts and a safety-focused environment are part of daily operations.

Qualificações

• High School diploma (mandatory).
• Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (mandatory).
• Relevant work experience.
• GMP-regulated QC laboratory experience (mandatory).
• GMP practices and HSE standards experience (preferable).
• Clear and open communication skills (written and verbal).
• Competent English (written and verbal).
• Ability and availability to work in shift patterns.

Responsabilidades

• Define and implement quality control techniques to verify the quality of Drug Product materials and associated analytical services in accordance with regulatory requirements.
• Organize and prioritize daily tasks to ensure accurate, timely testing and product release support.
• Adhere to laboratory testing schedules to achieve efficient QC system.
• Maintain data and records to GMP standards and internal procedures.
• Carry out routine calibration and maintenance of laboratory instruments and request parts as needed.
• Communicate with other departments using Hovione processes and IT platforms.
• Assist with audits as required and support QC investigations.

Descrição da oferta de emprego

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:

Defines and implements quality control techniques to verify the quality of Drug Product materials and associated analytical services in accordance with regulatory requirements. Performs Quality Control activities following quality standards, company procedures, client specifications, contract requirements, and regulatory guidelines. Organizes and prioritizes daily tasks to ensure accurate, timely, and compliant analytical testing and product release support.

• To organize and define daily priorities within their assigned tasks in order to accurately and promptly perform the allocated sample analysis to meet the requirements of the periodic laboratory plan and area KPIs.
• To adhere to the laboratory testing schedule in order to achieve an efficient Quality Control (QC) system.
• Take responsibility for all data individually generated and ensure it is in accordance with all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities.
• To maintain all checklists, laboratory records and notebooks in which he/she is involved to an acceptable GMP standard and in accordance with Hovione internal procedures.
• To maintain good hygiene and housekeeping within the laboratory.
• To perform routine calibration and both corrective and preventative maintenance of designated laboratory instruments, requesting any instrument parts and consumables required by the area.
• Comply with the high standards in the QC Laboratories.
• To bring any discrepancies, deviations or non-conformance in testing or work practice to the attention of QC management in accordance with Hovione internal procedures.
• To issue events and support the investigation of OOS/OOT/atypical results, deviations and QC incidents generated in the QC Laboratories.
• Ensure appropriate communication with other internal department in relation to QC work by using the appropriate Hovione processes and their IT platforms.
• Assist with audits as required, following the instruction of QC Management.
• Undertake any additional tasks to support the laboratory activities as and when required.
• Seek out additional information when one feels that the available information is not enough.
• Follow all annual performance review requirements, including completion of the self-assessment.
• Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice.
• Ensure facility activities are carried out in compliance with all GMP, legal and HSE regulations and applicable standards in the country of operation, complying with and enforcing all Hovione processes and good practice.

We are looking to recruit a Candidate:

• High School diploma (mandatory)
• Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (mandatory)
• Relevant work experience
• Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (mandatory)
• Experience of GMP practices and HSE standards (preferable)
• Technical understanding of GMP practices, analytical theory and techniques - Clear and open communication skills (written and verbal)
• Competent (written and verbal) English (preferable for sites where English is not the first language)
• Ability and availability to work in shift patterns, as required by business needs
• Computer literate with knowledge of the MS Office package AK382
• Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down.

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.