BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Chemist III to work for a leading San Diego biotechnology company.
The individual for this position will be responsible for the formulation and analytical development of injectable and solid oral drug candidates for human clinical studies. Previous development experience with peptides is desired. The individual should also have a basic understanding of lyophilization and differential scanning calorimetry (DSC). An individual at the level of Chemist III will be expected to take responsibility for the completion of projects under minimal supervision. The individual will be expected to develop time lines and plan series of experiments as required by service agreements and then coordinate and possibly delegate responsibilities to meet Client's expectations. The individual must have demonstrated proficiency in the development of one or more drug product dosage forms.
Essential Duties and Responsibilities include the following:
Conduct and/or supervise the execution of pre-formulation and formulation studies for injectables and solid oral drug candidates
Develop lyophilization cycles for injectable products
Develop stability-indicating HPLC analytical methods when appropriate
Prepare update documents and technical reports for clients
Develop strategic experimental plans and timelines
Understand the basics of GMP and IND enabling formulation strategies
Interpret data and use conclusions to propose follow up experiments
Lead technical discussions with clients
Effectively communicate with clients and interdepartmental colleagues
Education and/or Experience:
Bachelors degree in a physical or biological science, Chemistry preferred.
3-5 years of experience analytical techniques as follows:
HPLC, dissolution, lyophilization, and general wet chemistry experience such as: reversed-phase chromatography, ion-exchange chromatography, UV/Vis spectroscopy, and Karl Fischer analysis.
Current analytical methodology experience and/or knowledge of GLP and GMP regulations such as: proper GMP documentation, method qualification, test method preparation, product specification development for pharmaceutical products.
Strong written and oral communication skills.
Well organized, excellent time management, and PC and Microsoft Office proficient.
Contact email@example.com if interested, and visit www.biophaseinc.com to view all our current opportunities!
Monster - 16 months ago
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