Are you a highly skilled and experienced scientist with a passion for pharmaceutical development? We are seeking Development Scientists to play a key role in advancing our research and development initiatives. If you thrive in a collaborative environment, have a proven track record in polymer processing, particularly in injection molding or extrusion, and are driven by innovation, we invite you to apply and be a driving force in shaping the future of our company.

Sever Pharma Solutions is a global contract development and manufacturing organization (CDMO) for pharmaceutical products. We have ambitious plans for R&D expansion and are seeking two Development Scientists to contribute to our growing portfolio.

As a Development Scientist, you will be an integral part of our development team, reporting to the Director of Development. You will collaborate closely with cross-functional departments, including PMO, Engineering, Analytic Development, and QA, to drive product and production process development.

Responsibilities:

• Project member in the technical domain, driving product and production process development
• Conduct experiments and analyses to evaluate properties and performance of materials and polymer-based products
• Design and conduct scale-up trials to transfer processes from laboratory scale to commercial production
• Evaluate and implement new techniques and methods to enhance quality, efficiency, and cost-effectiveness in product and process development
• Collaborate with cross-functional teams to ensure smooth transitions between project phases and production

Qualifications and experience:

• PhD/MSc in Chemical Engineering, Material Science Engineering, Polymer Engineering, or related field
• Minimum 1 year highly relevant industrial experience
• Proven experience and proficient in polymer processing, including the development of extrusion processes and/or injection molding processes
• Excellent documentation skills
• Knowledge of pharmaceutical and/or medical device environments, including adherence to GMP, Design Controls and QbD, is desirable but not required

Example of tasks

• Establishing and maintaining routines, preparing technical and GMP related documentation, specifications, risk assessments and documenting activities related to manufacturing under GMP as well as technical manufacturing and verification activities.

About you:

We believe that important personal qualities for this role include being analytical, driven, adept at problem-solving, being a team player, exhibiting courage, and possessing strong communication skills.

To thrive at Sever Pharma Solutions, it's important that you share our three core values:

• Making a difference
• Best workplace
• Close to the customer

How to apply:

If you find that this description aligns with you and you're ready for a new adventure, we encourage you to submit your application by August 4^th. We are reviewing applications on an ongoing basis, so don't hesitate to send yours in.

Join us at Sever Pharma Solutions, where we're making significant investments in Research and Development (R&D) and fostering a collaborative and innovative environment.

About us:

Sever Pharma Solutions is a global contract development and manufacturing organization (CDMO) for pharmaceutical products. We offer customers bespoke solutions through extensive knowledge and unique manufacturing capabilities. Our expertise lies in developing and manufacturing polymer-based controlled release systems, sterile injectables, and solid dosage forms. Find more information on www.severpharmasolutions.com.