Sr. Bioprocess Engineer, Upstream
We are a growing and dynamic organization seeking a Process Engineer, Upstream to join our CMC organization. This position is responsible for developing and supporting processes for the manufacture of protein-based therapeutics. The individual will work with internal and external resources for the development of these processes and their transfer to clinical and commercial stage manufacturing plants.
Good things are happening at Omeros!
Come join our Omeros Team!
Who is Omeros?
Omeros is a commercial-stage biopharmaceutical company committed to discovering, developing and commercializing small-molecule and protein therapeutics for large-market and orphan indications targeting inflammation, complement-mediated diseases, disorders of the central nervous system and immune-related diseases, including cancers. In addition to its commercial product OMIDRIA (phenylephrine and ketorolac intraocular solution) 1%/0.3%, Omeros has multiple phase 3 and phase 2 clinical-stage development programs focused on complement-mediated disorders and substance abuse. Omeros also has a diverse group of preclinical programs including GPR174, a novel target in immuno-oncology that modulates a new cancer immunity axis recently discovered by Omeros. Small-molecule inhibitors of GPR174 are part of Omeros' proprietary G protein-coupled receptor (GPCR) platform through which it controls 54 new GPCR drug targets and their corresponding compounds. The company also exclusively possesses a novel antibody-generating platform.
What are your job responsibilities?
Your responsibilities in this position will include:
- Manage technical relationships with CMOs responsible for manufacturing GMP drug substance for Omeros
- Develop and scale up cell culture manufacturing processes suitable for both clinical use and commercial sale
- Responsible for supporting CMC aspects of the Company's drug substances from development through and including manufacturing
- Tech transfer of manufacturing processes to CMOs
- Troubleshoot cell culture, fermentation, and/or purification process and equipment challenges
- Act as Person in Plant (PIP) to oversee process development and manufacturing activities at CMOs (10-20% of time)
- Author drug substance related regulatory reports and submissions
- Ensure compliance with all applicable regulatory guidelines
- Must have the ability to build and maintain positive relationships with management, peers, and subordinates
- Excellent written and verbal skills required
- Must have integrity
- Must display strong analytical and problem-solving skills
- Attention to detail required
- BS or MS degree in chemical engineering or a related field or equivalent professional experience
- A minimum of 5 years of biotechnology and/or pharmaceutical industry experience. More experienced candidates are encouraged to apply
- Demonstrated knowledge of cell culture protein processing required
- Demonstrated problem solving capabilities
- Ability to navigate global regulatory CMC documents required
- Experience authoring CMC sections of regulatory submissions and participation in discussions with regulatory agencies preferred
- Participation in PAIs a plus
- Experience with cGMPs and Validation practices
- Experience with at least one biotechnology and/or pharmaceutical product launch is highly desirable
- Experience supporting regulatory inspections is desirable
- Good communication, managerial, analytical, planning, and organizational skills a must
- Demonstrated ability to work in a team environment
- Will aid in the supervision of activities at multiple CMOs. Responsibilities may include planning, assigning, and directing work at CMOs; and resolving problems that arise at CMOs
- Overnight travel, approximately 20% of the time, is required
- Intermittent physical activity including bending, reaching, pushing, pulling, or lifting up to 40 lbs.
- May encounter prolonged periods of sitting
- This position requires working with and near hazardous material
If you have the experience, skills and knowledge we are seeking, we'd love to hear from you! This is an exciting opportunity for the right person!
Omeros is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to status as a protected veteran or a qualified individual with a disability, or other protected status such as race, religion, color, national origin, sex, age, marital status, or any other factor determined to be unlawful by federal, state, or local statutes.
It is our policy to provide reasonable accommodation to anyone with a disability who needs assistance completing the job application process. If you need assistance, you can either send an e-mail to firstname.lastname@example.org or contact Omeros, asking for Human Resources, at (206) 676-5000.