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Associate

Thousand Oaks, CA
Top 3 Must Have Skill Sets:    

Analytical, data processing, HPLC or material characterization


Description:

Will begin onsite 100% after the 1st week of virtual orientation



Associate – Responsibilities include, but are not limited to, the following:
• Prepare formulations and perform dose analysis to support nonclinical pharmacokinetic, pharmacodynamic and toxicological studies.
• Design and conduct experiments for formulation development and molecule assessment including solubility, stability and solid state characterization per guidelines and instructions from project representatives.
• Providing hands-on formulation and process support during the development of clinical solid oral dosage forms
• Analyze data, maintain timely documentation (i.e. electronic notebooks), and contribute to technical reports and presentations in a matrixed team environment.
• Participate in lab housekeeping, maintain lab equipment and supplies, and comply with lab safety guidelines.
• May work occasionally on flexible schedule, i.e. starting early morning or finishing late evening, depending on the project need.


The ideal candidate would possess:
• Proficiency in liquid chromatography and common laboratory techniques (i.e. pH, microscopy).
• A fundamental understanding of drug formulation and physicochemical characterization.
• Experience with characterizing powder blends and solid oral dosage forms
• Attention to detail, adaptability to new techniques and multi-tasks, ability to solve problem and meet deadline, and effectiveness to work independently and as a team member.
• Strong computer skills in instrumentation and data processing in a client-server environment.
• Excellent interpersonal, communication (verbal and written) and organizational skills.


Basic Minimum Qualifications:
• B.S. or M.S. with 0-2 year experience with degree in Chemistry, Chemical Engineering, Pharmaceutics, Life Science or related scientific background. Pharmaceutical/biotech industry experience preferred.
• Skill in HPLC method and data analysis is essential. Experience in formulation development and/or solid state characterization is a plus.




Associate – Responsibilities include, but are not limited to, the following:
• Prepare formulations and perform dose analysis to support nonclinical pharmacokinetic, pharmacodynamic and toxicological studies.
• Design and conduct experiments for formulation development and molecule assessment including solubility, stability and solid state characterization per guidelines and instructions from project representatives.
• Analyze data, maintain timely documentation (i.e. electronic notebooks), and contribute to technical reports and presentations in a matrixed team environment.
• Participate in lab housekeeping, maintain lab equipment and supplies, and comply with lab safety guidelines.
• May work occasionally on flexible schedule, i.e. starting early morning or finishing late evening, depending on the project need.


The ideal candidate would possess:
• Proficiency in liquid chromatography and common laboratory techniques (i.e. pH, microscopy).
• A fundamental understanding of drug formulation and physicochemical characterization.
• Attention to detail, adaptability to new techniques and multi-tasks, ability to solve problem and meet deadline, and effectiveness to work independently and as a team member.
• Strong computer skills in instrumentation and data processing in a client-server environment.
• Excellent communication (verbal and written) and organizational skills.


Basic Minimum Qualifications:
• B.S. or M.S. with 0-2 year experience with degree in Chemistry, Chemical Engineering, Pharmaceutics, Life Science or related scientific background. Pharmaceutical/biotech industry experience preferred.
• Skill in HPLC method and data analysis is essential. Experience in formulation development and/or solid state characterization is a plus


"This posting is for Contingent Worker, not an FTE"

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