Quality Control Engineer (H/F)

About Recipharm : Recipharm is a leading global pharmaceutical CDMO (Contract Development and Manufacturing Organization), committed to helping pharmaceutical companies navigate the complexities of product development and manufacturing since 1995. Our expertise spans the entire product lifecycle, from early development to commercial production, ensuring precision and reliability at every step. With a dynamic workforce of over 5,000 professionals across 8 countries, we support our partners with end-to-end services that span drug development, clinical trials, manufacturing, and commercialization. Our facilities are strategically located across France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK, and the US, with continued growth on the horizon. Location: This VIE position is based in Watertown, Massachusetts, USA. Watertown is a small city a short bus ride 10 km west of Boston. Boston is an exceptional destination for young biotechnology professionals because it offers one of the world’s most dynamic life sciences ecosystems, combining cutting-edge research, innovative biotech startups, and global pharmaceutical companies within a highly collaborative environment. Boston also offers an international and welcoming community, excellent public transportation, a strong quality of life, and a rich cultural scene, making it easier to build both a successful career and a fulfilling personal life while contributing to groundbreaking discoveries that shape the future of medicine and healthcare. About the mission: We are offering a VIE mission of at least 1 year, with the possibility to extend up to 2 years, within our Quality Control (QC) department. You will report directly to the QC Director and play an essential role as a core team member supporting in-process, release, and stability testing of biopharmaceuticals in a GMP setting. This is a fantastic opportunity to be part of a global company ensuring the safety and quality of pharmaceutical products across all levels of clinical development, supporting contract manufacturers developing medicines to treat a wide variety of diseases.   Key Responsibilities: • Develop and implement a new stability storage management process • Develop and implement an incoming sample management process • Learn and master routine QC analytical testing of raw materials, in-process samples and finished products across a variety of methodologies including, but not limited to: o qPCR o ELISA o Microscopy o Environmental Monitoring • Learn to work within a GMP environment, following EMA and FDA guidelines. • Contribute to method qualification and troubleshooting endeavors. • Perform peer review of data. • Actively participate in Stability Program coordination and implementation • Collaborate across departments to coordinate contract testing and sample management activities • Gain in-depth knowledge of Recipharm’s group quality control processes, becoming familiar with the specific workflows that underpin our global operations. Profile: • Educational Background: Bachelor’s or Master's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences or related fields. • 0-3 years hands-on laboratory experience (academic or industry). • Exceptional documentation and data integrity habits, with a strong attention to detail. • Fluency in English: Proficient written and spoken English is a must. • Communication Skills: Excellent verbal and written communication skills with the ability to work well in a multicultural team. • Self-starter: Ability to work independently, manage priorities, and take initiative while remaining a team player. • Proficiency in MS Office: Strong skills in Excel and other MS Office applications. Useful Information: Upon joining, you will receive a comprehensive welcome and onboarding program at our Watertown site, where you’ll be introduced to both your future manager and local mentors who will support you throughout your journey. This hands-on training will ensure you are fully prepared for your role within the team. Additionally, Recipharm will participate in your monthly rent for your VIE accommodation, subject to certain limitations. These details will be discussed with you during the interview process, ensuring transparency and clarity. This VIE leads to a perspective of a permanent position within Recipharm, at Watertown or another site. Why to choose Recipharm : • International exposure: A unique opportunity to gain experience with a leading global player in the pharmaceutical industry. • Collaborative work environment: Work alongside passionate professionals in a welcoming, multicultural team. • Career development: Hands-on experience in a high-visibility strategic project, with the potential for long-term growth within Recipharm. We are committed to fostering a supportive environment where you can grow professionally and personally, while contributing to a transformative project with global impact.

• Educational Background: Bachelor’s or Master's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences or related fields. • 0-3 years hands-on laboratory experience (academic or industry). • Exceptional documentation and data integrity habits, with a strong attention to detail. • Fluency in English: Proficient written and spoken English is a must. • Communication Skills: Excellent verbal and written communication skills with the ability to work well in a multicultural team. • Self-starter: Ability to work independently, manage priorities, and take initiative while remaining a team player. • Proficiency in MS Office: Strong skills in Excel and other MS Office applications.

Recipharm is a leading global CDMO dedicated to meeting your evolving needs through operational excellence, scientific know-how, and customer connectivity. We operate development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK and the US and are continuing to grow and expand our offering. Our worldwide reach paired with in-depth, localised market knowledge allows us to anticipate our customers’ needs and strengthen the support we provide to forge a healthier, more expansive and more fruitful future together. With a workforce of 5 200 people, we are focused on supporting pharmaceutical companies with our full-service offering, taking products from early development through to commercial production. Since our inception in 1995, we have supported our customers throughout the entire product lifecycle, providing pharmaceutical expertise and managing complexity, time and time again to ensure their products are delivered with certainty.