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Associate Quality Control, Biopharma (JP10150)

West Greenwich, RI · Biotech/Pharmaceutical
Job Title:  Associate Quality Control, Biopharma (JP10150)
Location: West Greenwich, RI. 02817
Employment Type:  Contract
Business Unit: Quality Control, Bio-Analytics, and Raw Materials Testing
Duration: 3 years with likely conversion to FTE.

Posting Date:  04/28/2022
Notes:  Shift: Tuesday – Friday 7AM to 5PM, 10 hour shift schedule.

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 minimal supervision, this position will be responsible for activities including microbiology & analytical testing, sample and data management and equipment and instrumentation operation and maintenance in a highly dynamic, team environment. This position will be responsible for one or more of the following activities:
  1. Perform sample collection and sample handling to support GMP operations and Environmental/Water monitoring.
  2. Perform testing and possible data review for compendia, non-compendia methods, and routine laboratory procedures.
  3. Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks.
  4. Operate and maintain specialized laboratory equipment and instrumentation.
  5.  Participate in laboratory investigations and audits as necessary.
  6. Perform general laboratory housekeeping activities.
  7. Maintain training compliance and proficiency.
  8. At all times, comply with safety guidelines, cGMPs/CFRs and other applicable regulatory requirements
     
Basic Qualifications: Science related background, lab experience.


Why is the Position Open?
Staff Augmentation

Top Must-Have Skill Sets:
  • Lab experience, good documentation practices, experience working with passing/failing sample results.
  • This is an entry level position, however, they must have proven experience in Quality control.
  • Any science degree is considered
     
Day to Day Responsibilities:
  • Environmental sampling/Incubation, utilities sampling/testing,
  • Manufacturing sample collections, entering into clean room areas with QC equipment and ensuring all SOPs are being followed.

Employee Value Proposition:
The person in this role will work with the microbiology team. This team interacts in manufacturing and QC.

Red Flags:

Multiple jobs within a short period of time, issues working within a team.

Interview process:
Phone screening followed by in-person interview.


We invite qualified candidates to send your resume to recruiting@3keyconsulting.com.  If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
 

 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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