Position Summary:
ultradedicated – Your biggest challenges yield rare possibilities
In this role, you will be responsible for formulation, scale-up, technology transfer and supporting process development activities for Ultragenyx's growing biologic pipeline that require parenteral dosage form development. You will work with internal groups as well as with network of external vendors to manage formulation and drug product development activities. You will contribute to the Drug Product/Formulation function in CMC development teams to enable successful regulatory filings of new biologics.
Work Model:
Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site.
Responsibilities:
- Represent formulation and drug product function in internal and external CMC teams
- Design and perform lab-based experiments and activities to develop drug product formulations and manufacturing processes for Ultragenyx’s biologics products
- Work with CRO and CDMO in managing various aspects of the drug product development
- Design and conduct drug product process optimization including lyophilization, characterization, and clinical compatibility studies
- Author relevant drug product sections in regulatory filings and address agency questions
- Provide formulation and molecule support for Translational Research projects as appropriate
- Document laboratory experiments and results in lab notebooks and summarize findings in technical reports as needed
- Follow all safety and compliance regulations and company policies at work
Requirements:
- A degree in Biochemistry, Chemistry, Chemical Engineering, Bioengineering, Pharmaceutical Sciences or a related discipline
- PhD with 5-8 years, MS with 8-10 years, or BS with 10-12 years industry working experience. Job title is dependent on candidate’s experience level.
- Must have hands-on experience in formulation and DP process development for biologics
- Familiar with fill-finish processes, lyophilization development, clinical compatibility studies, scale-up and/or technology transfer
- Experience working with contract manufacturing and testing organizations is preferred
- Must have knowledge of analytical instrumentation used in biologics formulation development such as spectrometry, HPLC, CE, particle characterization techniques (HIAC, MFI, NTA), spectrometry, calorimetry, light scattering etc.
- Requires working knowledge of regulatory filings (IND/IMPD, BLA, MAA, being familiar with quality and regulatory requirements
- Experience in DOE statistical approach in formulation and process development is desired
- Experience in both early stage and late-stage process development is desired
- Must have excellent problem-solving skills and verbal and written communication skills
Physical Demands/Work Environment/Safety Considerations:
- Stand for extended periods of time with periodic stooping/bending / kneeling.
- Able to lift, push, pull up to 50lbs.
- Climb ladders and stairs of various heights.
- Work in a lab environment requiring special protective clothing over the head, face, hands, feet, and body. This role requires the ability to wear personal protective equipment.
- Certain tasks may require use of a respirator; medical clearance will be required in advance. #LI-CS1 #LI-Onsite
The typical annual salary range for this full-time position is listed below. This range reflects the characteristics of the job, such as required skills and qualifications and is based on the office location noted in this job posting. The range may also be adjusted based on applicant's geographic location.
This position is eligible for annual bonus and equity incentives. Actual individual pay is determined by demonstrated experience and internal equity alignment.
Ultragenyx Pharmaceutical is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at talentacquisition@ultragenyx.com.
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