Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

This early-career position will be responsible for key formulation/engineering support primarily dedicated to bench-scale formulations and process development activities associated with sterile injectable and lyophilized drug products, particularly liposomes and lipid-based formulations. The primary task would be to plan, support, and execute experiments with the aim of optimizing processes for scale-up and/or transfer to the cGMP environment within the constraints of timelines and under minimal supervision by senior scientific staff. A person with an innate scientific curiosity and keen observation skills will have the opportunity to impact the development of advanced medicinal prototypes for innovative drug delivery approaches. Additionally, the job responsibilities would include significant technical collaboration with the manufacturing and analytical technical services department as well as technical support for current process and product investigations.

• Execute developmental and investigational tasks through Quality by Design (QbD) approaches utilizing DOE principles. Associated tasks include formulation development, process design and engineering, equipment specification and engineering, data collection and analysis, generation and testing of critical process parameters (CPPs) to match the critical product attributes (CPAs) of the final drug product.
• Provide technical support via lab-scale execution for the manufacturing processes, including process investigations, process changes, and technical transfer and scale up of new product introductions. Adapt formulation solutions to complex products through guidance from senior scientific staff and collaborators
• Develop efficient, appropriate formulation procedures and Standard Operating Procedures (SOPs) for new equipment/processes as well as update of existing SOPs.
• Partner with the analytical technical services group to perform sample analyses in support of formulation development, in-process sampling and stability testing of final drug products/samples.
• Present quality written documentation, notebooks, methods, data reports and summaries. Report and treat data with a high level of integrity and ethics
• Discuss routinely with supervisor, project manager and peers the status of the assigned programs and potential problems. Communicate effectively on research results, issues, and plans.
• Conduct laboratory operations in a safe manner. Maintain compliance with the Chemical Hygiene Plan. Exhibit safety awareness and safe work practices.
• Follow responsible actions regarding chemical disposal in close collaboration with the EHS staff. Maintain compliance with appropriate SOP's.
• The person may also be expected to interface with external clients and contractors in support of existing projects.
• Performs special projects and other duties as assigned.

Physical Attributes:

• Regularly lift and /or move up to 10 pounds
• Frequently lift and/or move up to 25 pounds
• Specific vision abilities required by this job include close vision, distance vision, color vision and peripheral vision
• Ability to climb stairs and ladders to perform the functions of this job

Who You Are:

Minimum Qualifications:

• Bachelor's Degree in Chemical Engineering, Biochemical Engineering, Bioengineering, Pharmaceutical Sciences, Polymer Science, or Material Science, or other Engineering discipline
• 1+ years' experience in pharmaceutical process and formulation development or academic research activities in planning and executing protocols

Preferred Qualifications:

• Proficiency in the use of LIMS and/or Minitab
• Ability to independently perform root cause analysis for investigations
• Experience with statistical designs of experiments (DOE) methodology
• Strong problem-solving skills and proficiency in general wet chemistry techniques and hands-on skills
• Experience in collecting data and accurately maintaining laboratory notebooks
• Advanced computational skills with spreadsheets, word processing and databases
• Strong verbal and written communications skills
• Effective interpersonal skills to interface with internal and external clients as well as outside contractor
• Ability to work and make decisions independently as well as with a team
• Ability to work in technically demanding situations
• Well organized with excellent time management skills to effectively coordinate multiple projects concurrently

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html