Scientist I / II (f/m/d) - In-Use studies and PPM Testing

Purpose of your Job

As part of our dynamic Formulation Development & Analytics unit, you will directly contribute to enabling the next generation of biopharmaceutical therapies. Our team drives innovative formulation and analytical strategies under BSL‑1/2 and S1/S2 safety levels, as well as GMP quality standards. By joining us, you will help ensure that advanced scientific work is carried out with excellence, precision, and curiosity.
This role plays a key part in shaping Coriolis Pharma’s global growth - including our build‑up of new U.S. facilities in North Carolina’s Research Triangle Park (RTP), one of the world’s most vibrant biotech innovation hubs. You will be involved in transferring expertise, establishing scientific capabilities, and supporting the seamless integration of processes across locations.

In this position, you will transform scientific questions into meaningful analytical insights. You’ll develop and implement state‑of‑the‑art methods, interpret complex data, and influence the scientific direction of client projects in an international, highly collaborative environment. Throughout your journey, you’ll be supported in growing your technical strengths (e.g., analytical method development, instrumentation, troubleshooting) as well as your personal skills (e.g., project ownership, communication, organization).
This opportunity is ideal for someone who enjoys hands‑on laboratory work, thrives in a project‑driven setting, and is excited about contributing to both scientific excellence and the establishment of a new, forward‑looking site in the U.S!

Your Responsibility

• Be part of project teams for client projects (e.g., liquid/lyophilization formulation development, comparability and stress testing, storage stability study) as assigned by the superior with special focus on in‑use stability studies and primary packaging material (PPM) testing :
  • Work as (i) 1st, 2nd project leader and/or (ii) team member for projects.
  • Contribution/responsible for the development of work plans, testing procedures and/or amendments for customer projects.
  • Correctly, timely and independently plan and execute formulation preparation / analytical testing / experiments.
  • Independently perform analytical method transfer/implementation.
  • Demonstrate solid understanding of performed analytical methods and be able to apply the knowledge to interpret the data.
  • Perform data analysis and subsequently put data into context for data presentation and/or report.
  • Support scientific discussion in client meeting.
  • Appropriately act on unforeseen events.
    
    
• Be specialist / expert on several instruments / analytical methods / application areas (e.g., able to perform method development, interpretation of data, troubleshooting and training of new users).
• Implementation of new analytical equipment / technologies and application of the methods within client projects.
• Support on-boarding of new team members.
  • Liaise with superior on training needs.
  • Act as mentor.
• System Owner for laboratory equipment: responsible for operator training, equipment maintenance, calibration and qualification.
• Ensures that GRP rules are followed and documented.
• Ensures general laboratory cleanliness.
• Other duties as assigned by superior.

What you need to succeed

• University degree in pharmaceutical sciences, (bio)chemistry, biology, or a related field
• Minimum 3 years of relevant experiences, e.g. employment in pharmaceutical industry / analytical laboratory (e.g. CDMO) or PhD studies
• Experience with equipment commissioning, maintenance, and LIMS
• Proven track record and hands- on experience in planning and executing in-use stability studies and PPM comparability testing is strongly preferred
• Proficiency in HPLC/UPLC-analysis (SEC, IEX, RP, LC-CAD), CE-analysis and subvisible particle analysis (MFI, LO) highly beneficial
• Additional expertise in biophysical characterization (AUC, CD, µDSC, FTIR, fluorescence), osmolality and turbidity is a plus
• Knowhow in biopharmaceutical formulation development beneficial
• Strong verbal and written communication skills
• Good knowledge of English (both written and spoken)
• Good time management and prioritization skills
• Eagerness to learn and develop new skills
• Open-minded and able to adapt strategies to changes
• Strong intercultural and interdisciplinary team player
• Strong problem-solving skills
• Hands-on mentality: practical, solution-oriented approach with a willingness to take initiative
• Candidates must be based in North Carolina (NC) or willing to relocate to NC

Invest in yourself

Let’s formulate innovation together…
Our success & development is created by the people working together @Coriolis. We put People first! That’s why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and customers.

We would like to grow together with you!
Let’s continue building and creating the future now! Join our Team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience. We offer an attractive work space at the Martinsried site. Let’s make a difference together!

Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, sex, citizenship or gender identity, color, disability, religion/belief, sexual orientation, marital status, age or individual preferences. Different backgrounds, experiences and ideas push us further and raise the bar.

Thank you for your interest! We look forward to receiving your application documents.
Please use our career portal exclusively for this purpose.
We would like to support you from the very beginning to shape your development possibilities here at Coriolis.
For questions or further information, please visit our website or contact us directly.

We are looking forward to your application!

Your Contact

Dominik Schwemmer Senior Business Partner - Talent & Development
People, Organization & Culture Unit

Coriolis Pharma Research GmbH
Phone: +49 (0) 89 – 417760 - 0
Fraunhoferstraße 18 b, 82152 Martinsried

About us

Coriolis Pharma is a global contract research and development organization (CRDO) and a premier partner for the development of liquid and lyophilized drug products, analytical services, and manufacturing services across a vast array of therapeutic modalities, including biologics, gene and cell therapies and vaccines.

Our scientists design and execute platform and custom services to accelerate and derisk our clients’ programs right from the start and throughout the entire product lifecycle.

Our company culture is based on diversity, teamwork and open and appreciative communication. That's why wonderful people from over 36 nations around the world work together successfully at Coriolis.
Our headquarters are located in Martinsried near Munich, Germany. An additional project management and business development team in the United States enables our US clients to work seamlessly with our German offices.

What motivates us? Our motivation is to improve the quality of life for humankind by enabling the development of innovative drugs through outstanding biopharmaceutical services from preclinical to commercialization