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Job Title: Specialist System Administrator – (JP10214)
Location: West Greenwich, RI. 02817
Employment Type: Contract
Business Unit: Operations DTI
Duration: 1+ years (with likely extensions)
Notes: Hybrid schedule. Must come on site to West Greenwich, RI. facility
Posting Date: 05/05/2022
3 Key Consulting is hiring a Specialist System Administrator for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
Day to Day Responsibilities:
Support systems administration activities for benchtop applications
Provide end user support, grant access to GMP systems
Employee Value Proposition:
Red Flags:
No regulatory environment experience, no GMP experience. See top skill sets and description.
Interview process:
Phone screening followed by in-person 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.
Location: West Greenwich, RI. 02817
Employment Type: Contract
Business Unit: Operations DTI
Duration: 1+ years (with likely extensions)
Notes: Hybrid schedule. Must come on site to West Greenwich, RI. facility
Posting Date: 05/05/2022
3 Key Consulting is hiring a Specialist System Administrator for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
- 2+ years of experience within Pharma or Biotech.
- Benchtop experience highly preferable.
- Must have GMP environment experience, application administration.
- Ability to follow procedure and revise/ create procedures as needed.
- Bachelor’s Degree.
- Provide end user support, grant access to GMP systems.
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
- 2+ years of experience within Pharma or Biotech.
- Benchtop experience highly preferable.
- Must have GMP environment experience, application administration.
- Ability to follow procedure and revise/ create procedures as needed
- Bachelors Degree.
Day to Day Responsibilities:
Support systems administration activities for benchtop applications
Provide end user support, grant access to GMP systems
Employee Value Proposition:
- Unique experience.
- Good opportunity to understand client standard technology & to exposure to other sites.
Red Flags:
No regulatory environment experience, no GMP experience. See top skill sets and description.
Interview process:
Phone screening followed by in-person 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.