- Location
- West Greenwich, RI
- Type
- Contract
- Department
- Healthcare
- Seniority
- Entry
- Education
- Associate
- Source
- CATS
Description
Job Title: Associate Quality Control, Biopharma (JP10361)
Location: West Greenwich, RI
Employment Type: Contract
Business Unit: QC Microbiology, QC Support for Mfg, Sample Management/Stability
Duration: 12 months with likely extensions
Job posting date: 06/07/2022
Note: Shift is Sat, Sun, Mon, Tue 7:00 AM- 5:00 PM
3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
Job Summary:
Under general supervision, this position will perform routine procedures and testing in support of the QC for manufacturing Operations A Team, performing sample collection and microbiology testing.
This position will be responsible for one or more of the following activities:
Basic Qualifications
Top Must have Skill Sets:
Worker will travel throughout production areas collecting samples to bring back to microbiology lab for testing, following all SOPs, and GMP / GDP expectations.
Employee Value Proposition:
The person in this role will learn all aspects of microbiology testing, trouble shoot problems and practice teamwork. This is a great entry level role to get into the Biotech/Pharma industry.
Red Flags: No relevant experience.
Interview Process:
Interview via Webex with camera on.
We invite qualified candidates to send your resume to [email protected]. If you decide that you’re not interested in pursuing this position, please feel free to take a 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
Employment Type: Contract
Business Unit: QC Microbiology, QC Support for Mfg, Sample Management/Stability
Duration: 12 months with likely extensions
Job posting date: 06/07/2022
Note: Shift is Sat, Sun, Mon, Tue 7:00 AM- 5:00 PM
3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
Job Summary:
Under general supervision, this position will perform routine procedures and testing in support of the QC for manufacturing Operations A Team, performing sample collection and microbiology testing.
This position will be responsible for one or more of the following activities:
- Performing routine laboratory procedures
- Daily sample collection, testing, and entry into manufacturing (clean) space.
- Routine analytical testing
- Documenting, computing, compiling, interpreting and entering data
- Maintaining and operating specialized equipment
- Initiating and / or implementing changes in controlled documents.
- Must 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 logbooks.
Basic Qualifications
- Associates degree and 2 YOE
- Bachelor’s degree and some lab experience (Recent college graduates welcome)
Top Must have Skill Sets:
- Lab Experience/academia or outside of school
- Positive
- Willing to learn
- Aseptic experience preferred but not required
Worker will travel throughout production areas collecting samples to bring back to microbiology lab for testing, following all SOPs, and GMP / GDP expectations.
Employee Value Proposition:
The person in this role will learn all aspects of microbiology testing, trouble shoot problems and practice teamwork. This is a great entry level role to get into the Biotech/Pharma industry.
Red Flags: No relevant experience.
Interview Process:
Interview via Webex with camera on.
We invite qualified candidates to send your resume to [email protected]. If you decide that you’re not interested in pursuing this position, please feel free to take a 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
Skills
GMP
