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Associate Quality Control, Biopharma (JP100108)
West Greenwich, RI · Biotech/PharmaceuticalJob Title: Associate Quality Control, Biopharma (JP100103)
Location: West Greenwich, RI. 02817
Employment Type: Contract
Business Unit: Quality Control, Bio-Analytics, and Raw Materials Testing
Duration: 1+ years (with likely extensions)
Posting Date: 04/20/2022
Notes: 100% onsite. Must have proven Quality Control experience (not just in the summary on the resume).
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 Raw Material Instrumentation group. This position will be responsible for one or more of the following activities:
Why is the Position Open?
Additional workload.
Top Must-Have Skill Sets:
This is an entry level position, however, they must have proven experience in Quality control.
Any science degree is considered
Day to Day Responsibilities:
Basic Qualifications:
Quality control lab experience and use of HPLC/UPLC equipment is preferred
Red Flags:
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: Quality Control, Bio-Analytics, and Raw Materials Testing
Duration: 1+ years (with likely extensions)
Posting Date: 04/20/2022
Notes: 100% onsite. Must have proven Quality Control experience (not just in the summary on the resume).
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 Raw Material Instrumentation 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.
- 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?
Additional workload.
Top Must-Have Skill Sets:
- Must have Quality Control lab experience and understanding of GMP expectations
- HPLC and UPLC experience
- Positive attitude and understanding of fast paced environment
This is an entry level position, however, they must have proven experience in Quality control.
Any science degree is considered
Day to Day Responsibilities:
- Routine lab upkeep
- Routine lab testing and operations
- Maintain training
Basic Qualifications:
Quality control lab experience and use of HPLC/UPLC equipment is preferred
Red Flags:
- R&D experience only.
- Frequent job changes.
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.
Regards,
3KC Talent Acquisition Team