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Sr Process Engineer DSP, MTS
1 week ago
Evotec WD Redmond, United StatesSr Process Engineer DSP, MTS page is loaded · Sr Process Engineer DSP, MTS · Apply · locations · Redmond · Seattle · time type · Full time · posted on · Posted 2 Days Ago · job requisition id · JOB ID-10109 · Process Engineer 3, Downstream–Site MSAT · | Just. – Redmo ...
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Sr Process Engineer DSP, MTS
1 week ago
Just - Evotec Biologics Redmond, United StatesProcess Engineer 3, Downstream-Site MSAT · | Just. - Redmond, WA and Seattle, WA | · Just-Evotec Biologics is seeking a highly motivated Downstream Process Engineer for site MSAT to join a fast-paced, collaborative, and multidisciplinary team. The role report to Downstream Lead ...
Sr Process Engineer DSP, MTS - Seattle, United States - Evotec WD
Description
Sr Process Engineer DSP, MTS page is loadedSr Process Engineer DSP, MTS
Apply
locations
Redmond
Seattle
time type
Full time
posted on
Posted 2 Days Ago
job requisition id
JOB ID-10109
Process Engineer 3, Downstream–Site MSAT
| Just. – Redmond, WA and Seattle, WA |
Just-Evotec Biologics is seeking a highly motivated Downstream Process Engineer for site MSAT to join a fast-paced, collaborative, and multidisciplinary team.
The role report to Downstream Lead for site MSAT, and will be responsible to support all aspects of downstream processing for multiple clinical-scale cGMP manufacturing trains employing the innovative Just-Evotec continuous processing platform in 24/7 operations.
Roles and responsibilities:
Represents site MSAT on project teams as technical subject matter expert (SME) and interface with global MSAT, Operations and Quality functions.
Authors, reviews and owns process related documentation (technical documents, test protocols, batch records, process descriptions, SOPs, etc)
Authors, reviews change controls including managing change implementation of the change as the assigned change agent.
Partner with Quality, Validation and Global MSAT to develop and implement process validation and comparability study activities leading to successful product registration.
Act as a subject matter expert for regulatory and client inspection audits.Utilize technical skills and process knowledge to participate and/or lead investigations related to process/ New product implementation. Collaborate with impacted groups to drive implementation of CAPAs from approval to closure & effectiveness check.
Monitors and reports on process performance data analysis
Ability to share 24/7 on call support activities during production.
Apply Operational Excellence principles to lead continuous improvement for downstream process improvements.
Position Requirements:
Masters (or Bachelors) degree in Engineering with years of
pharmaceutical/biotech
experience including a minimum of 2-4 years of supporting downstream purification activities for biopharmaceutical products.
Knowledge and experience CMC stage gates for clinical and commercial biologics drug substance manufacturing programs.
Proven record of accomplishment and self-directed leadership in GMP pharmaceutical or biotechnology is required.
Technical purification and solution preparation operations using disposable-based manufacturing technologies
Demonstrated capabilities to work with high-performing teams, drive change, and influence internal and external stakeholders
Extensive knowledge of US FDA CFRs and European EMA, including ICH guidelines, as they relate to drug substance biological manufacturing
Good interpersonal, team, and collaborative skills are required.
Excellent verbal and written communication skills in English; ability to interface with all levels of the organization
Additional Preferred Qualifications:
Experience in supporting audits and inspections by health authorities, clients and other external auditors as a presenter or audit support staff.
Entrepreneurial drive to achieve business objectives.
The base pay range for this position at commencement of employment is expected to be $ 111,360 to $159,000
; Base salary offered may vary depending on individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.
Evotec (US) Inc. is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.
About Us
Just – Evotec Biologics, wholly owned by Evotec SE, is a first-to-industry biologics platform that leverages AI/ML technologies and world-leading molecular design, cell line development, process intensification and continuous manufacturing strategies to advance biotherapeutics from discovery through clinical stages to commercial launch.
The Just – Evotec Biologics team combines deep industry experience in the fields of data, protein, process, and manufacturing sciences including automation with highly integrated and flexible capabilities to break through the scientific and economic barriers associated with the development of protein therapeutics.
Our focus is to accelerate and expand access to biotherapeutics through scientific and technological innovation for our proprietary projects and on behalf of our partners.
Learn more at.
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