logo

View all jobs

Senior Associate, Scientific GMP (JP9309)

Thousand Oaks, CA · Biotech/Pharmaceutical
Job Title: Senior Associate, Scientific GMP (JP9309)
Location: Thousand Oaks, CA
Employment Type: Contract
Business Unit: Drug Product Supply, Manufacturing
Duration: 12 months with likely extensions
Job posting date: 10/13/2021
Note: Onsite Essential

3 Key Consulting is hiring a Senior Associate for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.

Job Summary:
Under minimal supervision, responsible for one or more of the following activities in Manufacturing:
  • Analytical testing, characterization, sample and data management.
  • Equipment maintenance
  • Contributes to team by ensuring the quality of the tasks/services provided by self
  • Contributes to the completion of milestones associated with specific projects or activities within the team.
  • Support manual visual inspection of filled units
  • This role will support manufacturing operations, as such some extended hours, shift, and weekend work flexibility may be necessary as required.
     
Day-To-Day Responsibilities:
  • Manual visual inspection operations
  • Analytical testing
  • Plan and perform routine analyses with efficiency and accuracy.
  • Plan and perform multiple, complex routine/non-routine methods and procedures and a large variety of assays.
  • May perform aseptic aliquoting, sampling and analysis of compendia methods
  • Perform accurate laboratory/manufacturing documentation following GMP guidelines.
  • With a high degree of technical flexibility, work across diverse areas within the lab.
  • Evaluate analytical data
  • Perform general lab/area housekeeping
  • Maintain/operate specialized equipment
  • Comply with safety guidelines, GMPs and other applicable regulatory requirements
  • Initiate and/or implement changes in controlled documents
  • Troubleshoot, solve problems and communicate with stakeholders
  • Participate in audits, initiatives, and projects that may be departmental or organizational in scope
  • Evaluate lab practices for compliance and operational excellence improvements on a continuous basis
  • May participate in lab/inspection deviation investigations
  • May own deviation/CAPA records
  • May provide technical guidance
  • May train other staff
  • May contribute to regulatory filings
  • May represent the department/organization on various teams
  • May interact with outside resources
  • Support manual visual inspection of drug product filled units
  • Deepens technical knowledge trough exposure and continuous learning
     
Basic Education:
  • Bachelor’s degree in Life Sciences & minimum 2 years of biotech industry QC experience/GMP laboratory/manufacturing (preferably in manual visual inspection) experience.
  • Experience with regulatory compliance in GMP manufacturing and testing of pharmaceutical products.
Skills:
  • Take initiative to identify and drive improvements
  • Excellent verbal and written communication skills
  • Strong technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)
  • Presentation skills
  • Escalate issues professionally and on a timely basis
  • Decision making skills
  • Teamwork and coaching others
  • Negotiation and influencing skills
  • Project management and organizational skills
  • Ability to interact with regulatory agencies
  • Data trending and evaluation
  • May set project timeframes and priorities based on project objectives and ongoing assignments. Recognizes and escalates problems.
  • Ability to work independently and deliver right the first-time results
  • Follows procedures. Refers to technical standards, principles, theories and precedents as needed.

Top Must have Skill Sets:
  • GMP experience (Preferably in biotech or similar industry)
  • Laboratory/analytical background (Preferably in biotech or similar industry)
  • Detailed-oriented/Problem solving/Troubleshooting

Employee Value Proposition:
Chance to gain experience and have high visibility

Red Flags:
  • No GMP experience
  • No schedule flexibility
  • Unable to work in a team environment
  • Lacking communication skills
     
Interview Process:
First phase - phone interview
If needed may request virtual interview



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
 
 
Powered by