Senior Scientist-Process Development Jobs
By Pfizer At Groton, CT, United States
PhD in chemistry with 0-5 years experience in the pharma industry.
Experience with applying biocatalysis in a laboratory setting.
Working experience designing and optimizing biocatalytic reactions, high-throughput screening in multi-well plates and developing new enzyme platforms.
Non-standard Work Schedule, Travel Or Environment Requirements
Responsible for coaching, mentoring, training, supervising, and developing staff when assigned; participate in recruiting when needed.
Prepares research reports and technical presentations and external publications.
Engineer Ii - Upstream Process Development
By Mori At Boston, MA, United States
Management experience in a research environment
Manage upstream team with up to five full time employees
Base salary range from $95,000 - $115,000 based on experience
Experience with lab scale reactors
Analytical laboratory and protein analysis experience preferred
Excellent organizational, communication, and teamwork skills
Senior Associate Scientist, Process Development - Downstream
By Forge Biologics At Columbus, OH, United States
Prepare sterile reagents as dictated by procedures or management by filtration or steam autoclaving.
Reports any discrepancies from protocols/study procedures or any materials preparation problems to management.
Practical experience with FPLC (Fast Protein Liquid Chromatography)
Experience with other aspects of downstream purification (e.g. – clarification/filtration, TFF, etc.)
Experience with lab, pilot, and large-scale FPLC systems.
Experience with the purification of vaccines or viral vectors.
Scientist I/Ii, Downstream Process Development
By Encoded Therapeutics Inc. At South San Francisco, CA, United States
Offer guidance and lab-level leadership for incumbent associates, with possibility for 1-2 direct report(s)
May include approximately 20% remote work, with flexibility based on project needs
BS+8 / MS+6 / PhD+2 years minimum industry experience in a process development or MSAT role
Excellent communication and presentation skills. Capability to convey complex technical information in a clear, concise, and influential manner
Prior experience developing purification processes for virus, VLP, or gene therapy vectors for GMP clinical manufacturing.
Working knowledge of the GMP manufacturing environment, which may include involvement in process transfer, review of batch records/deviations/CAPAs, or ‘person-in-plant’ duties.
Scientist, Ii Jobs
By AbbVie At Lake County, IL, United States
Demonstrated scientific writing skills and strong verbal communication skills.
Synthesis, purification and characterization of ADCs on mg to gram scale under minimal supervision.
Optimization and validation of conjugation protocols and formulation buffers.
Optimization of automated techniques for ADC synthesis and purification.
Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions.
Demonstrated ability to learn, understand and master new experimental techniques.
Engineer Ii, Process Development
By Moderna At , Norwood
Vacation, sick time and holidays
Volunteer time to participate within your community
Paid sabbatical after 5 years; every 3 years thereafter
Here’s What You’ll Bring to the Table:
Generous paid time off, including:
Scientist Ii Jobs
By Bausch + Lomb At , Rochester, 14651

This position may be available in the following location(s):

Development Scientist Ii, Analytical Development And Clinical Qc
By AstraZeneca At , New Haven, 06510
Experience in analysis of various Biologic modalities (e.g., mAb, antibody-drug conjugate, fusion protein)
Extensive experience in separations science (e.g., SEC, RP, IEX). Experience in Molecular biology (PCR, DNA extraction) and immunoassay (ELISA) techniques.
Experience of testing strategy for late-stage program in preparation for BLA filing
Excellent written skill for drafting all the GMP related documents.
Ensure communications occur with stakeholders and partners for all the analytical topics
Author analytical method transfer/validation related protocols and reports for late stage clinical and commercial programs.
Lead Scientist/Director, Upstream Process Development, Expat In South Korea
By Laguna Source At Greater Boston, United States
* 8+ years of Biotechnology industry experience leading upstream mammalian cell culture process development.
* Experience leading cross-functional, multi-national teams including tech transfer teams.
* Competitive base salary, target bonus, retirement allowance and excellent medical benefits.
Preferred Candidate Background and Expertise:
* MS or Ph.D. in Chemical Engineering, Biochemistry, Molecular Biology, Biology or related Life Sciences field.
* Ability to build and maintain strong, positive relationships with customers.
Associate Scientist Ii, Biologics Drug Product Development
By ABBVIE At , Irvine
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
CMC development experience in protein formulation, drug delivery, or analytical functions is preferred
Prior experience with drug product manufacture processes and lyophilization is a plus
Execute formulation composition and drug product process development studies for sterile liquids, lyophilized, and pre-filled dosage forms
Manufacture drug product formulation batches for evaluating formulation stability and/or to support animal studies
Conduct clinical in-use studies to guide dose solution administration
#Scientist Ii Jobs
By ABBVIE At , Barceloneta, Pr
Ability to manage multiple priorities and comply with deadlines.
Maintains their certifications as needed for assigned job tasks.
Demonstrates strong analytical skills and logical thought processes.
Assists in troubleshooting multi-discipline problems.
Applies scientific/engineering principles applicable to assigned tasks and problem-solving.
Independently design, execute and interpret critical experiments to answer scientific questions.
Scientist/Engineer Ii Jobs
By HNTB Corporation At , Kansas City, 64106, Mo
Bachelor's degree in Engineering and 2 years of relevant experience, or
Master’s degree in Engineering and 1 year of relevant experience
Engineer in Training (EIT) certification
Click here for benefits information: HNTB Total Rewards
Completes assigned work within the schedule and number of hours provided.
Responsible for preparation and/or modification for select portions of project reports, plans, designs, and calculations.
Sr. Associate Scientist, Process Development
By Gilead Sciences At La Verne, CA, United States
Strong project management and organizational skills.
Leads technical support activities related to maintaining commercial product supplies through management of internal and external resources.
Knowledge of GMP and regulatory requirements of biopharmaceutical manufacturing is preferred.
Contributes to user requirement specification and provides expert process technical support to utilize and validate new and improved technologies.
Experience with statistical data analysis tools is preferred.
Excellent troubleshooting skills and ability to solve complex technical issues.
Scientist I - Process Development
By PCI Pharma Services At Bedford, NH, United States
Collaborates with Process Development Scientists and Management during technical transfer and experiment design.
Responsible for reviewing executed documentation for accuracy and completeness prior to submission to management.
Assists with the implementation of Process Development strategies as directed by management
Expected to adhere to all procedures, including gowning and safety requirements, at all times
Strong oral and written communication skills
Knowledge of Current Good Manufacturing Processes (cGMP), Regulatory Guidelines, Aseptic Manufacturing, as well as bulk intermediate and medical device manufacturing.
Engineer Ii, Process Development
By Moderna At Norwood, MA, United States
Experience in laboratory work and knowledge of appropriate laboratory hygiene
Prior co-op or internship experience in related industry is favorable
Knowledge of bioprocess engineering principles, processes, and analytical techniques
Knowledge of statistical Design of Experiment (DoE) concepts and analysis of multivariate data
Preferred: Hands on experience with AKTA FPLC, Tangential flow filtration (TFF), and HPLC/UPLC instrumentation
Effective communication skills and the ability to write detailed technical reports
Scientist Ii Jobs
By CRISPR Therapeutics At Boston, MA, United States
Generate, manage, evaluate, and maintain critical data in a highly organized manner, providing statistical analysis and troubleshooting where appropriate.
PhD in Molecular Biology or another related discipline with 2-5 years of relevant experience
Extensive experience using molecular biology techniques, such as PCR, dPCR and TIDE
Proficiency in cell & tissue culture (cell lines; experience with hepatocyte culture is a plus), transfection,
Experience with protein extraction, and western blots
Knowledge of CRISPR/Cas9 Gene Editing
Senior Scientist, Upstream Process Development
By Akron Biotech At Sarasota, FL, United States
Exceptional time management and multi-tasking skills.
Provide technical information and experimental assay design; data analysis and management; and instrument & project troubleshooting.
Supporting the Process Development team in the following: time management and prioritization
In addition to competitive compensation, we offer a comprehensive benefits package including:
Experience in development of pDNA and recombinant products for cGMP manufacturing.
Minimum 5+ years of experience in upstream or downstream PD in an advanced contributor role.
Research Associate Ii - Vaccine Process Development
By BioSpace At Boston, MA, United States
Education, Experience, Knowledge And Skills
Personal motivation to expand applicable scientific knowledge through reading and by attending seminars and research meetings.
Experience with analytical methods used in process development is strongly desired.
Working knowledge of Biologics cGMPs including ICH guidance documents would be a distinct advantage
Good oral and written communication skills are required.
Typical laboratory bending, stooping, lifting requirements apply.
Sr Scientist - Vaccine Process Development
By BioSpace At Boston, MA, United States
Education, Experience, Knowledge And Skills
Good time and project management skills, ability to execute or oversee several studies simultaneously.
Design, manage, lead, and execute studies pertaining to Process Development.
Lead, train, and provide work direction to other Scientists, Research Associates, and Interns. May be required to manage junior scientists.
Experience in laboratory scale process science, including process scale-up and scale-down required.
Knowledge of cGMP practices as applicable to process development, formulation, analytical development, technology transfer, or manufacturing would be a distinct advantage.
Scientist, Virology Upstream Process Development
By Catalent Pharma Solutions At Baltimore, MD, United States
Develops and executes large-scale productions and harvest protocols. Utilizes technical knowledge to scale up to manufacturing scales.
Uphold the EHS requirements of this position.
Medical, dental and vision benefits effective day one of employment
Catalent offers rewarding opportunities to further your career!
Degree field in Chemical Engineering, Biochemical Engineering, Chemistry, or Life Science field
Ph.D. – 0-3 years; MS – 3-6 years; BS - 6-9 years

Are you looking for an exciting opportunity to join a leading biopharmaceutical company and make a real impact on the development of innovative medicines? We are looking for an Upstream Process Development Scientist II to join our team and help us develop and optimize upstream processes for the production of biologics. You will be responsible for designing and executing experiments to characterize and optimize cell culture processes, developing and validating analytical methods, and providing technical support to manufacturing operations. If you have a passion for biotechnology and a strong background in upstream process development, we want to hear from you!

Upstream Process Development Scientist II is a job that involves developing and optimizing bioprocesses for the production of biopharmaceuticals. This job requires a strong understanding of bioprocessing principles, techniques, and technologies. The Scientist II must be able to design, develop, and implement upstream processes for the production of biopharmaceuticals.

What is Upstream Process Development Scientist II Skills Required?

• Knowledge of bioprocessing principles, techniques, and technologies
• Ability to design, develop, and implement upstream processes
• Knowledge of cell culture and fermentation processes
• Knowledge of process analytical technologies
• Ability to troubleshoot and optimize processes
• Ability to work in a team environment
• Ability to communicate effectively

What is Upstream Process Development Scientist II Qualifications?

• Bachelor’s degree in biotechnology, biochemistry, or related field
• 3+ years of experience in bioprocessing
• Experience in cell culture and fermentation processes
• Experience in process analytical technologies
• Knowledge of cGMP and regulatory requirements

What is Upstream Process Development Scientist II Knowledge?

• Knowledge of bioprocessing principles, techniques, and technologies
• Knowledge of cell culture and fermentation processes
• Knowledge of process analytical technologies
• Knowledge of cGMP and regulatory requirements