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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:
Why is the Position Open?
Staff Augmentation
Top Must-Have Skill Sets:
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.
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:
- Perform sample collection and sample handling to support GMP operations and Environmental/Water monitoring.
- Perform testing and possible data review for compendia, non-compendia methods, and routine laboratory procedures.
- Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks.
- Operate and maintain specialized laboratory equipment and instrumentation.
- Participate in laboratory investigations and audits as necessary.
- Perform general laboratory housekeeping activities.
- Maintain training compliance and proficiency.
- At all times, comply with safety guidelines, cGMPs/CFRs and other applicable regulatory requirements
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
- 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.