Analyst

Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market.

Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites.

Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life.

As an Analyst, you will play a key role in ensuring the integrity and compliance of raw materials, with occasional support to other departments as needed. You will be responsible for implementing and executing quality control techniques to verify the quality of raw materials, intermediates, and final products, in line with regulatory requirements and client expectations.

Key Responsibilities:

• Define and prioritize daily tasks to ensure timely and accurate sample analysis aligned with lab schedules and KPIs.
• Perform analytical testing in accordance with GMP, HSE regulations, and internal SOPs.
• Maintain accurate and compliant laboratory records, notebooks, and checklists.
• Ensure cleanliness and organization of the laboratory environment.
• Conduct routine calibration and maintenance of lab instruments, and manage necessary consumables.
• Identify and report discrepancies, deviations, or non-conformances in testing or practices.
• Support investigations of OOS/OOT/atypical results and other QC incidents.
• Collaborate with internal departments using established communication platforms and processes.
• Assist during audits and contribute to continuous improvement initiatives.
• Stay informed and proactive when information is incomplete or unclear.
• Adhere to all safety, environmental, and GMP regulations and standards.

• High School diploma (mandatory)
• Degree in Chemistry, Analytical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field (mandatory)
• Proven experience in a GMP-regulated QC laboratory, preferably in the pharmaceutical or related industry
• Strong understanding of GMP practices, analytical techniques, and HSE standards
• Proficient in English (written and verbal) and MS Office tools
• Willingness to work in shifts as required by business needs

This role is ideal for professionals who are detail-oriented, quality-driven, and eager to contribute to a high-performing QC team with a strong focus on raw materials.

Hovione is a proud Equal Opportunity Employer

Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.