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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:

Role Purpose

Responsible for defining and implementing Quality Control (QC) techniques to ensure the quality of raw materials, intermediates, and finished products. The role supports analytical services in compliance with GMP, regulatory requirements, and client specifications, ensuring all QC activities meet high standards of quality, safety, and efficiency.

Analytical & Technical Activities

• Execute and support analytical projects, including:

• Method development, transfer, validation, and optimization

• Protocol and report preparation

• Perform analytical testing using techniques such asHPLC, GC, and other laboratory instrumentation

• Interpret analytical data ensuring compliance with documentation standards and regulatory expectations

• Propose and implement new methodologies based on project needs

• Troubleshoot analytical issues and escalate when required

Quality & Compliance

• Ensure full compliance withGMP, GLP, ICH guidelines, and internal procedures

• Manage deviations, CAPAs, and investigations in a timely and structured manner

• Review team documentation to ensure accuracy, completeness, and procedural adherence

• Maintain laboratory records, logbooks, and systems to audit-ready standards

• Participate in audits and inspections as required

Project & Stakeholder Management

• Manage assigned tasks and projects efficiently, ensuring delivery:

• On time

• Within budget

• According to quality standards

• Act as a liaison between QC and internal/external stakeholders

• Ensure proactive communication and effective information flow across teams

Laboratory Operations

• Perform equipment maintenance, calibration, and qualifications

• Maintain laboratory systems (e.g., LIMS, Empower) and ensure data integrity

• Uphold laboratory housekeeping and safety standards

• Contribute to KPI tracking and continuous improvement initiatives

Collaboration & Leadership

• Work collaboratively within cross-functional teams

• Support onboarding and training of new team members

• Promote a culture ofquality, safety, and continuous improvement

• Act as a role model for professionalism and compliance

Health, Safety & Environment (HSE)

• Adhere to all HSE policies, procedures, and regulatory requirements

• Identify and report risks, deviations, or unsafe conditions

Promote safe laboratory practices at all times

We are looking to recruit a Candidate:

• Degree inChemistry, Chemical Engineering, Pharmaceutical Sciences, Biochemistry, or related field(mandatory)

• Background in aQC laboratory environment

• Hands-on experience inanalytical chemistry(preferred)

• Exposure toGMP and ICH standards(preferred)

• Knowledge of:

• HPLC, GCand analytical techniques

• Analytical method lifecycle (development, validation, transfer, review)

• GMP practices and data integrity principles

• Familiarity withEmpowerand laboratory information systems (desirable)

• Strong attention to detail and documentation skills

• Problem-solving and analytical thinking

• Ability to manage multiple priorities effectively

• Team collaboration and communication skills

• Proactive mindset with continuous improvement orientation

• Fluency inEnglish

• Proficiency inMS Officetools

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, pleasecontact 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 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.

(https://en-careers-hovione.icims.com/jobs/11898/qc-associate/job?mode=apply&apply=yes&in\_iframe=1&hashed=-1834418400)

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Hiring Request Post Information* : Posted Date2 months ago(2026/6/11 13:28)

ID2026-11898

of Openings1

Job LocationsPT-Loures

Job FamilyQUALITY