logo

View all jobs

Associate Quality Control (JP8288)

Thousand Oaks, CA · Biotech/Pharmaceutical
Job Title:  Associate Quality Control (JP8288)
Location: Thousand Oaks, CA. (Onsite Essential)
Employment Type:  Contract
Business Unit: ATO Quality Control Chemistry and Biochemistry
Duration:  months (with likely extensions)
Posting Date: 2/25/21
 
 
3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.
 
Job Description:
Under general supervision, this position will perform routine procedures and testing in support of the High Throughput lab (HTL) group. This position will be responsible for one or more of the following activities:
 
  • Performing routine laboratory procedures
  • Routine analytical testing
  • Documenting, computing, compiling, interpreting and entering data
  • Maintaining and operating specialized equipment
  • Initiating and / or implementing changes in controlled documents.
 
Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books.
 
Why is the Position Open?
Supplement additional workload on team.
 
 
Top Must-Have Skill Sets:
  • Must have bachelor’s degree & 1-3 years of industry experience, open to the industry - manufacturing, cosmetics, pharma, biotech etc.
  • Must have cGMP Experience & Experience in general compendia testing
 
 
Day to Day Responsibilities:
  • Routine analytical testing
  • Documenting, computing, compiling, interpreting and entering data
  • Maintaining and operating specialized equipment
  • Initiating and / or implementing changes in controlled documents.
  • General Lab housekeeping
 
 
Basic Qualifications:
  • Some lab experience is preferred.
  • Must have bachelor’s degree & 1-3 years of industry experience.
  • Open to the industry - manufacturing, cosmetics, pharma, biotech etc.
  • Must have cGMP Experience & Experience in general compendia testing.
 
 
Employee Value Proposition:
A person in this role will have the opportunity to do testing and document revisions. There is an opportunity to add to your skill set.
 
 
Red Flags:
  • Lack of experience in GMP area.
  • Long distance travelling.
  • Not flexible in terms of working hours.
 
 
Interview process:
Video Skype Panel Interview.
 
 
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
Powered by