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Sr Associate Quality Control (JP9532)
Thouasand Oaks, ca · Biotech/PharmaceuticalJob Title: Sr Associate Quality Control (JP9532)
Location: West Greenwich, Rhode Island
Employment Type: Contract
Duration: 2 years +
Job posting date: 12/6/2021
Note: Onsite Essential
3 Key Consulting is hiring a Sr Associate Quality Control for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
Job Summary:
Day-To-Day Responsibilities:
Top Must have Skill Sets:
Red Flags: Jumpy job history
Interview Process:
Interviews will be conducted via Webex. First interview with hiring manager, second interview with team
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
Location: West Greenwich, Rhode Island
Employment Type: Contract
Duration: 2 years +
Job posting date: 12/6/2021
Note: Onsite Essential
3 Key Consulting is hiring a Sr Associate Quality Control for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
Job Summary:
- Candidate will be working on site
- Targeting candidates with 4-6 years of industry/ non academia experience
- Quality Control Raw Materials is searching is for an analytical scientist to support testing for Raw Materials of routine samples for use within our network manufacturing operations.
- This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.
- The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.
Day-To-Day Responsibilities:
- Performing analytical testing for HPLC, UPLC, Gas Chromatography, GC-MS and/or IC-PMS
- Interacting cross-functionally with a wide variety of people and teams
- Troubleshoot, solve problems and communicate with stakeholders.
- Participate in initiatives and projects that may be departmental or organizational in scope.
- Evaluate lab practices for compliance and operational excellence on a continuous basis.
Qualifications - 4-6 years of experience in HPLC, GC, GC-MS and/or ICP/MS.
- Bachelors Degree in any science field.
- Demonstrated experience in investigations and QC processes.
- Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision.
- Strong communication skills (both written and oral), facilitation and presentation skills.
- Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories, preferably with GMP experience.
- Compendial experience.
- Understanding of biopharmaceuticals process and related unit operations
- Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.
- Independent, self-motivated, organized, able to multi-task in time-sensitive environments.
Top Must have Skill Sets:
- HPLC, GC, GC-MS or ICPMS experience, pertaining to routine use and troubleshooting
- GMP laboratory experience
- Teamwork and motivation to problem solve and improve self, operations, and processes
Red Flags: Jumpy job history
Interview Process:
Interviews will be conducted via Webex. First interview with hiring manager, second interview with team
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team