Scientist I, Analytical Development
Company: Omeros Corporation
Location: Seattle
Posted on: May 14, 2022
Job Description:
Scientist I, Analytical Development This position will primarily
be responsible for the development, transfer, qualification, and
validation of potency bioassays in support of clinical development
and commercialization of antibody therapeutics. The Scientist may
also contribute to the development, transfer, and qualification /
validation of impurity ELISAs and analytical HPLC and/or CE methods
to monitor physicochemical quality attributes for both protein and
small-molecule therapeutics. The individual will develop and
implement methods for characterization, contribute to tech transfer
to clinical and commercial stage CROs / CMOs, and provide input to
and manage external CROs who may develop and implement methods for
characterization, release, and stability testing. Come join our
highly talented CMC Team and help shape the future of Omeros! About
Omeros Corporation Omeros is an innovative biopharmaceutical
company committed to discovering, developing and commercializing
small-molecule and protein therapeutics for large-market and orphan
indications targeting inflammation, immunologic diseases (e.g.,
complement-mediated diseases) and cancers. Omeros' lead MASP-2
inhibitor narsoplimab targets the lectin pathway of complement and
is the subject of a biologics license application pending before
FDA for the treatment of hematopoietic stem cell
transplant-associated thrombotic microangiopathy. Narsoplimab is
also in multiple late-stage clinical development programs focused
on other complement-mediated disorders, including IgA nephropathy,
atypical hemolytic uremic syndrome and COVID-19. OMS906, Omeros'
inhibitor of MASP-3, the key activator of the alternative pathway
of complement, is in a Phase 1 clinical trial. For more information
about Omeros and its programs, visit . Your specific job
responsibilities will include:
- Analytical method development, testing, transfer,
qualification, and validation in a GLP and/or GMP environment
- Troubleshoot typical method and equipment challenges
- Write standard test methods, technical reports summarizing
analytical data, and qualification / validation reports
- Participate in cross-functional teams as a representative of
the Analytical Development group
- Assists in trouble-shooting CMC-related problems from CROs /
CMOs
- Assists in investigations involving data generated internally
and by CROs / CMOs
- Ensures laboratory equipment is calibrated and maintained in
proper working order to enable compliance with GLP and/or GMP
environments
- Contribute to drafting regulatory submissions
- Ensures compliance with all applicable regulatory guidelines
Education and Experience needed:
- Demonstrated knowledge and experience developing potency ELISAs
for protein therapeutics and interpreting data is required
- Knowledge and experience transferring, troubleshooting, and
validating assays is required
- Knowledge and experience developing HPLC and/or CE based
methods is a plus
- Small and large molecule experience is desired
- Demonstrated problem-solving capabilities
- Knowledgeable in global regulatory CMC documents
- Familiar with GMPs and qualification / validation
practices
- ---1 (for Ph.D.) or ---8 (for B.S.) years of biotechnology
and/or pharmaceutical industry experience required
- BS, MS or Ph.D. in biology, biochemistry, analytical chemistry,
or a related field
- Experience with "start-up" biopharma company desirable
- Excellent communication, analytical, and organizational skills
required Behavioral Competencies Required:
- Must have the ability to build and maintain positive and
collaborative relationships with management and peers
- Excellent written and verbal communication skills required
- Must display strong analytical and problem-solving skills
- Attention to detail required Physical Demands 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
This is an opportunity for you to be a key member of a
collaborative group contributing your talent and expertise to a
company that has an exciting pipeline. If you have the knowledge,
skills and experience we are looking for, we'd love to hear from
you! 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 or contact Omeros, asking for Human Resources, at .
Keywords: Omeros Corporation, Seattle , Scientist I, Analytical Development, Other , Seattle, Washington
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