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Quality Control Senior Associate (JP8256)

West Greenwich, RI · Biotech/Pharmaceutical
Job Title:  Quality Control Senior Associate (JP8256)
Location: West Greenwich, RI (Onsite Essential)
Employment Type:  Contract
Business Unit: ARI QC Lab Assurance & Systems
Duration: 1+ year with likely extensions
Posting Date: 2/18/21
 
 
3 Key Consulting is hiring a Senior Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.
 
Job Description:
The Rhode Island Quality Control Equipment group is responsible for the end to end life cycle of equipment in QC. This includes procurement, development, and execution of validation and change control strategy, oversight of general and preventative maintenance activities, and decommission support as required.


The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.
 
Responsibilities will include, but are not limited to:
  • Monitor and trouble shoot analytical benchtop equipment.
  • Execute Work Orders and interact routinely with end customers and vendors to ensure
    the reliability of QC equipment support in a fast-paced environment.
  • Support and sometimes lead projects to implement new equipment.
  • Work autonomously to support cross-functional projects and help to identify end-user
    requirements, validation requirements, and Change Control Strategy.
  • Complete all assigned tasks on time, in collaboration with key stakeholders.
 
What we are looking for:
  • Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.
  • Demonstrated ability to work independently and deliver right first-time results
  • Excellent communication skills (written and verbal)
  • Must have focus on data integrity and cGMP practices
  • Qualified to work in the U.S. without employer sponsorship
  • Commitment of a 40-hour work week in West Greenwich, RI
 
Preferred Qualifications
  • GMP and GDP experience in a laboratory setting.
  • Proficient in, Maximo, CDOCS, LIMS
  • Experienced in Quality systems, including Deviations, CAPA, Change Control
  • Experienced in Quality processes, including validation and data integrity
  • Proficient in problem solving and LEAN principles
 
 
Why is the Position Open?
Supplement additional workload on team.
 
Top Must-Have Skill Sets:
  • GMP and GDP experience in a laboratory setting
  • Troubleshooting equipment preferred
  • Attention to detail, excellent communication skills
 
Employee Value Proposition:
Experience with change control and other systems.

 Red Flags:
Candidates with no experience outside of college. 
 
Interview process:
Phone screening of possible candidates. Possible second phone screen and/or virtual interview for those who pass the initial phone screening.
 
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
 
 
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