Job Information
Hovione Quality Assurance Associate - Temporary Assignment in Loures, Portugal
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:
Guarantees cGMP compliance in all activities and systems related to Projects and Products execution. Assures that working practices are streamlined and aligned with the actual needs of each project. Implements policies, procedures and methods to evaluate and to continuously improve the quality of products and operations throughout the products lifecycle. Provides global supplier qualification services in support of new product introduction and existing products. Collaborates with suppliers and Procurement to assure the quality of their products, materials, components and/or operations.
Manage quality activities to ensure compliance with cGMP and legal regulations, keeping the site audit-ready.
Promote high-quality standards and foster a culture of continuous improvement across company operations.
Prepare for and support internal and external audits, ensuring consistent inspection readiness.
Prepare, review, and approve SOPs, IOPs, protocols, reports, and regulatory documentation as needed.
Participate in key quality activities for assigned projects and new product introductions.
Monitor and ensure timely closure of deviations and approval of change controls (PdAs).
Facilitate effective communication between stakeholders and support compliance issue resolution.
Maintain regular presence in manufacturing areas, providing hands-on support and fostering collaboration.
Investigate customer complaints and support the generation and reporting of team KPIs.
Ensure safe practices and compliance with HSE standards in all assigned tasks and responsibilities.
We are looking to recruit a Candidate:
University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar scientific field (mandatory).
Requires educational / training experience in a QA GMP environment within the Pharmaceutical Industry (desirable).
Experience of working in a GMP operational environment (desirable).
Fluency in English is a requirement.
Computer literate with good working knowledge of the MS Office package
Good documentation skills and attention to detail
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 (https://www.hovione.com/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.
(https://en-careers-hovione.icims.com/jobs/11483/quality-assurance-associate---temporary-assignment/job?mode=apply&apply=yes&in\_iframe=1&hashed=-1834418400)
Hiring Request Post Information* : Posted Date2 days ago(2026/4/21 11:46)
ID2025-11483
of Openings1
Job LocationsPT-Loures
Job FamilyQUALITY