As a Hardware & Automation Field Application Scientist (FAS) within BioProduction, you will be a trusted technical partner to biotechnology and biopharmaceutical customers helping them evaluate, implement and adopt technologies that improve bioprocess performance.
Locations (2)
Ireland
United Kingdom
Responsibilities
Act as a technical expert and trusted advisor for BioProduction hardware, single-use systems and automation.
Support workflow development and technology integration across upstream and downstream processing, focusing on upstream bioprocessing equipment and single-use systems.
Support customers with process engineering, scale-up and scale-down, technology transfer, process optimization and troubleshooting.
Lead or contribute to pre- and post-sales technical activities, including workflow assessments, hardware evaluations, proof-of-principle studies, demonstrations, pilot runs and technology qualification.
Troubleshoot process, hardware, single-use flow-path and automation issues.
Process Integration Intern within the Keysight Labs/High Frequency Technology Center, contributing to next-generation heterogeneous integration and advanced packaging technologies.
Compensation
(PhD) CA Pay Range-$55.14 - $59.38
Responsibilities
Assisting with the planning, execution, and documentation of engineering experiments to evaluate process, material, and equipment performance.
Collecting, analyzing, and interpreting process, defectivity, metrology, and electrical test data to identify trends and improvement opportunities.
Investigating process integration challenges and supporting root cause analysis of yield, quality, and reliability issues.
Collaborating with process, equipment, yield, metrology, and product engineers to drive continuous improvement initiatives.
Evaluating the interaction of process steps across the manufacturing flow and assessing their impact on device performance, yield, and manufacturability.
Requirements
Graduate student pursuing M.S. or Ph.D. in Electrical Engineering
Graduate student pursuing M.S. or Ph.D. in Mechanical Engineering
Graduate student pursuing M.S. or Ph.D. in Chemical Engineering
Graduate student pursuing M.S. or Ph.D. in Materials Science
Graduate student pursuing M.S. or Ph.D. in Chemistry
Skills
Director, Process Development (Pivotal & Commercial)
Lead and manage the purification development strategy for pivotal, commercial, and lifecycle-management biologics programs, providing scientific and technical direction across scale-up, validation readiness, technology transfer, and commercial manufacturing support.
Compensation
The salary range for this position is: $226,185.00 - $292,710.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Responsibilities
Define and execute purification development strategy for a portfolio of pivotal, commercial, and lifecycle-management biologics programs.
Provide scientific and technical direction for process development, characterization, scale-up, validation readiness, technology transfer, and commercial manufacturing support.
Oversee development of robust and manufacturable drug substance purification processes, including harvest clarification, chromatography, virus inactivation, virus filtration, ultrafiltration/diafiltration, formulation, and final drug substance filtration.
Direct risk-based process characterization strategies, scale-down model development, process parameter evaluation, and establishment of scientifically justified process control strategies.
Provide technical support for technology transfers to internal manufacturing sites, external partners, and contract development and manufacturing organizations.
Requirements
Principal Scientist Chemistry, Small Molecule Process Development and Manufacturing
Seeking a highly motivated and creative Chemist to lead and mentor scientific and engineering teams in the development of robust processes for the synthesis of Small Molecules from early to late phase drug development.
Compensation
The base compensation range for this role is: $159,000.00-$219,000.00
Responsibilities
Lead collaborative development for manufacturing teams to design and conduct laboratory experiments to optimize and characterize processes of Biogen assets
Design and lead experimental planning to advance the Biogen portfolio
Lead project teams towards the implementation of safe, efficient and robust chemical processes of Biogen drug candidates
Mentor less experienced staff by promoting the use of key laboratory instrumentation
Develop fundamental process knowledge to support the transition of chemical and biochemical processes from laboratory scale to manufacturing partners
Principal Mechanical Engineer - Manufacturing Process to provide technical leadership for the development, characterization, validation and production readiness of manufacturing and assembly processes for complex precision electromechanical products.
Compensation
Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Ireland: 81,120.00 EUR - 121,680.00 EUR | The final salary within this range will be determined based on objective, job-related criteria, including relevant experience, skills and qualifications, in accordance with our compensation framework. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
Responsibilities
Own manufacturing and assembly process development across multiple related product lines, from early lab development and pilot-line builds through validated Manufacturing release and ramp-up.
Develop a deep understanding of product design, critical characteristics, tolerance chains, component variation, interfaces and product-process interactions.
Translate product requirements and design intent into robust process flows, assembly concepts, operating windows, acceptance criteria and control strategies.
Lead lab and pilot-line builds, DOE, process characterization, optimization, capability studies and structured technical investigations.
Establish and maintain process risk and control documentation, including process flows, PFMEA, control plans, work instructions and supporting engineering evidence.
Requirements
Bachelor’s or advanced degree in Mechanical, Manufacturing, Mechatronics or a related engineering discipline
Performs all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs.
Compensation
Salary Range (hourly) $22.21 - $34.71
Responsibilities
Assists and/or contributes in all areas of production as needed
Monitors production processes including cell culture and purification activities for drug substance manufacturing and filling, and inspection and packaging activities for drug product manufacturing
Reviews, edits, completes and revises completed batch records, logbooks and SOPs in accordance with cGMP standards
Ensures availability of production batch records for upcoming lots
Performs manufacturing-level maintenance and cleaning of equipment
Requirements
BS/BA in Life Sciences or related field
AS/AAS in Biotechnology/Biological Science or equivalent combination of education and experience
Lead a team of engineers to support high-volume manufacturing processes and drive advancements within Intel's next-generation packaging technologies.
Compensation
Annual Salary Range for jobs which could be performed in the US: $120,860.00-231,670.00 USD
Responsibilities
Lead and manage a team of engineers to support safe, high-volume manufacturing processes while driving continuous improvements in quality, output, cost, and yield.
Provide tactical direction and prioritize activities for sustaining operations, systematic troubleshooting, and process optimization.
Collaborate with cross-functional engineering and manufacturing teams to address integrated process and equipment challenges.
Develop and mentor engineers, cultivating technical expertise, leadership skills, and long-term growth opportunities within the team.
Facilitate technology transfer and ensure matched processing across global sites through training sessions and audits.
Requirements
Bachelor's degree in engineering, materials science, physics, or a related technical field
PhD in chemical engineering, biochemical engineering, biochemistry, bioengineering, biotechnology, pharmaceutical sciences or related scientific discipline
MS with 10+ years of relevant experience
BS with 12+ years of relevant experience
Nice to have: direct people leadership experience
Nice to have: supporting pivotal or commercial-stage monoclonal antibodies, complex proteins, bispecific antibodies, antibody-drug conjugates
Semiconductor R&D Process Integration InternKeysight · Santa Rosa, US