Analytical Tech Transfer Associate IIAlthea Technologies, Inc. - San Diego, CA
Let’s Make Things Happen!
Ajinomoto Althea, Inc. is a fully integrated contract development and manufacturing organization providing clinical drug process development and manufacturing services to global biotechnology and pharmaceutical companies.
Althea is a leading expert in aseptic filling of drug product in vials and syringes, and our focused expertise and capabilities make us one of the industry’s top leaders for cGMP microbial fermentation of recombinant proteins and plasmid DNA. In conjunction with these manufacturing operations, Althea offers comprehensive development services including: upstream and downstream process development, complex formulations, lyophilization cycle, analytical development, product release and ICH-compliant stability testing.
Now is an exciting time to join Althea. We have talented people working together to help our clients advance their innovative product pipelines. We believe that people are our greatest asset and we are committed to providing our employees with an environment that fosters personal and professional growth.
Our work atmosphere is fast paced, stimulating and customer focused. Employees take pride in knowing our efforts are helping countless patients for years to come.
Althea is currently seeking an Analytical Tech Transfer Associate II
to transfer, qualify, and validate analytical methods and maintain analytical instrumentation. This position regularly exercises technical discretion in design, execution, and interpretation of experiments.
Transfers, qualifies, and validates analytical methods and maintains analytical instrumentation with minimal supervision.
Responsible for performing technical transfer experiments for projects and products in collaboration with others.
Uses professional concepts in accordance with company objectives to solve complex problems in creative and effective ways.
Investigates, creates, and develops new methods and technologies for project advancement under limited supervision.
Exercises technical discretion in design, execution, and interpretation of experiments that contribute to project goals.
Creates and updates SOP’s, Protocols, and reports.
Contributes to project progress within scientific discipline through innovative research.
Maintains laboratory notebooks, prepares technical reports, summaries, protocols and quantitative analyses.
May provide guidance to junior personnel.
Provides training and guidance to Quality Control during the transfer of methods.
Acts as the technical SME for internal/external clients.
Applies established principles, theories and concepts in area of responsibility, together with a working knowledge of related disciplines.
Responsible for identifying patentable inventions and acting as investigator in conducting his or her own experiments.
Embodies Althea’s cultural values by aligning daily actions with department goals and company culture.
Bachelor’s degree in a Life Sciences discipline or equivalent.
One to three (1-3) years of relevant experience in biotechnology.
cGMP knowledge needed and strong data review skills and knowledge of data integrity a plus.
Familiarity with Agilent ELN and Chromeleon HPLC application a plus.
Detail oriented and strong written and verbal communication skills.
Ability to work independently, within prescribed guidelines, or as a team member.
Demonstrated ability to follow detailed directions in a laboratory environment.
Must be familiar with Microsoft Office applications.
If you meet the requirements above, and would like to apply for this position, please visit our website at www.altheacmo.com and click on the Careers section. Please be sure to note where you saw our ad posting.
We are an EOE dedicated to a diverse work force and Drug Free work environment.
Qualified M/F/D/V candidates are encouraged to apply.
8 days 10 hours ago
Althea Technologies, Inc.
Please review all application instructions before applying.
Althea Technologies, Inc., based in San Diego, CA, is focused on reducing the time, risk, and overall cost of our partner's drug development efforts. We apply immediate resources, unsurpassed scientific expertise, and a vast knowledge of regulatory affairs to facilitate the progression from drug discovery to clinical approval. Althea was founded in 1998 with the purpose of accelerating drug development by providing reliable, high quality services to the biotechnology and pharmaceutical industry. With our founders' well-known expertise in gene quantification and biopharmaceutical development, we began offering custom real-time qPCR assay services and plasmid DNA production. Today, Althea has established itself as a leading provider of these highly technical services. Our continued growth has enabled us to expand our service portfolio and more than double our manufacturing capacity.
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