logo

View all jobs

Associate Project Management – Biotech Small Molecule (JP7900)

Thousand Oaks, CA · Biotech/Pharmaceutical
Job Title: Associate Project Management – Biotech Small Molecule (JP7900)
Location: Thousand Oaks, CA    
Employment Type: Contract
Duration: 12 months with likely extensions
Business Unit: External Process Development
Job posting date: 11/10/2020
Note: Remote until COVID-19 restrictions are lifted.
 
3Key Consulting is hiring an Associate Project Management for a consulting engagement with our client, a leading global bio-pharmaceutical company.


Ideal candidate:
  • 5+ years of synthetic/ small molecule experience
  • Synthetic (Small Molecule) Drug Substance and Drug Product Method Development
  • Synthetic (Small Molecule) Drug Substance and Drug Product Stability Study Knowledge
  • Synthetic (Small Molecule) Drug Substance and Drug Product Method Qualification
  • Strong communication
  • Must hold a minimum of a B.S. in Biology/Chemistry or related field.
     
Description:
The External Process Development organization is seeking a highly qualified candidate to support analytical assay outsourcing associated with execution of external development and clinical supply. The position will be a key enabling role in a high performing cross functional organization. The associate will be responsible for supporting analytical demand for assay execution related to stability and development.

Analytical background in drug substance/product testing. Experience in small molecule (synthetics). knowledge of stability testing for those products. Familiar with ICH guidelines and GMP/GLP testing.
Must hold a minimum of a B.S. in Biology/Chemistry or related field.
This person will be interacting with outsourced partners and must have excellent communication skills. Ability to multitask.

Top Must have Skill Sets:
  • Synthetic (Small Molecule) Drug Substance and Drug Product Method Development
  • Synthetic (Small Molecule) Drug Substance and Drug Product Stability Study Knowledge
  • Synthetic (Small Molecule) Drug Substance and Drug Product Method Qualification
 
Day-To-Day Responsibilities:
Day to day oversite of analytical programs at external vendors including:
  • Set up new drug substance and drug product programs (method development, feasibility, and qualification) at external vendors
  • Movement of materials/samples between sites
  • Ownership of PO’s, invoices and budget accounting
  • Overseeing investigations and deviations that occur
  • Set up new and oversee existing stability studies at the site
  • Overseeing standard and sample inventory at the site
  • Maintain metrics (method tracking, project tracking)

Employee Value Proposition:
Candidate will be overseeing synthetic processes, leading investigating's and working within a team environment
 
Red Flags:
No Analytical Experience - lack of top 3 skills - lack of years of experience - not local candidates
 
Interview Process:
Phone screening then Video
 
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
 
 
 
Regards,
 
3KC Talent Acquisition Team
 
 

Share This Job

Powered by