Scientist, Process Development Downstream at Lonza America Inc in Houston, TX
Lonza is seeking a highly motivated senior level process scientist with diverse experiences in biological processes. The candidate must have biopharmaceutical industry experience with developing, optimizing, and characterizing downstream processes including various chromatography methods. The successful candidate will participate in all facets of downstream process development for a wide array of viral vectors, including adeno-associated virus (AAV). Key
Responsibilities:
Interact with new or existing Cell and Gene Therapy clients to document and transfer new processes to Lonza sites and communicate. Lead and support scientific or engineering expertise toward the design and development of new process ideas that support client product concepts. Provide technical and scientific leadership to other team members. This includes providing assistance to management in the design of new, unique or existing protocols. Oversee the initial technical training of specific Process protocols to the Manufacturing Teams. Lead, review and/or train/assist in writing and revising technical documents including laboratory SOPs, protocols, reports and batch records. Key requirements:
PhD in Life Sciences with focus on biology or Bioengineering with advanced years of related manufacturing or process development experience in biotech industry experience; MS degree in Life Sciences field and expertise in manufacturing or process development experience in biotech industry. Demonstrated downstream process development experience of biological molecules, such as viral vectors, therapeutic recombinant proteins, monoclonal antibodies or vaccines for biopharmaceutical applications is required. A deep knowledge, and understanding of downstream process of biologics including various chromatography methods are required. Experience of chromatographic principles and systems:
HPLC, FPLC Experience with the operation and development of TFF, UF/DF, and filtration:
Repligen, SciLog Working knowledge and skills for viral vector or vaccine purification is a plus. Ability to plan, organize, problem solve (troubleshoot), design experiments, prioritize, work efficiently independently and in a team under tight timelines. Experience or knowledge of analytical methods and in process controls commonly used in viral vector manufacturing. Self-directed and self-motivated; demonstrated ability to work both independently and also as a team member in a matrix environment; maintains a positive approach to setbacks and challenges; champions new ideas and initiatives; brings out and utilizes others' creativity to improve team performance. Client oriented:
establishes effective and responsive relationships with all clients; able to translate client projects into a feasible process design. Excellent computer software skills related to Microsoft office and data analysis; keep professional, accurate and timely records of all essential activities; able to manage multiple projects; excellent time management skills.
Salary Range:
$80K -- $100K
Minimum Qualification
Life SciencesEstimated Salary: $20 to $28 per hour based on qualifications.
Responsibilities:
Interact with new or existing Cell and Gene Therapy clients to document and transfer new processes to Lonza sites and communicate. Lead and support scientific or engineering expertise toward the design and development of new process ideas that support client product concepts. Provide technical and scientific leadership to other team members. This includes providing assistance to management in the design of new, unique or existing protocols. Oversee the initial technical training of specific Process protocols to the Manufacturing Teams. Lead, review and/or train/assist in writing and revising technical documents including laboratory SOPs, protocols, reports and batch records. Key requirements:
PhD in Life Sciences with focus on biology or Bioengineering with advanced years of related manufacturing or process development experience in biotech industry experience; MS degree in Life Sciences field and expertise in manufacturing or process development experience in biotech industry. Demonstrated downstream process development experience of biological molecules, such as viral vectors, therapeutic recombinant proteins, monoclonal antibodies or vaccines for biopharmaceutical applications is required. A deep knowledge, and understanding of downstream process of biologics including various chromatography methods are required. Experience of chromatographic principles and systems:
HPLC, FPLC Experience with the operation and development of TFF, UF/DF, and filtration:
Repligen, SciLog Working knowledge and skills for viral vector or vaccine purification is a plus. Ability to plan, organize, problem solve (troubleshoot), design experiments, prioritize, work efficiently independently and in a team under tight timelines. Experience or knowledge of analytical methods and in process controls commonly used in viral vector manufacturing. Self-directed and self-motivated; demonstrated ability to work both independently and also as a team member in a matrix environment; maintains a positive approach to setbacks and challenges; champions new ideas and initiatives; brings out and utilizes others' creativity to improve team performance. Client oriented:
establishes effective and responsive relationships with all clients; able to translate client projects into a feasible process design. Excellent computer software skills related to Microsoft office and data analysis; keep professional, accurate and timely records of all essential activities; able to manage multiple projects; excellent time management skills.
Salary Range:
$80K -- $100K
Minimum Qualification
Life SciencesEstimated Salary: $20 to $28 per hour based on qualifications.
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