Apply to Quality Control Senior Associate - Capillary Electrophoresis (JP10023)

Job Title: Quality Control Senior Associate - Capillary Electrophoresis (JP10023)
Location: West Greenwich, RI.
Employment Type: Contract
Business Unit: QC Bioanalytics & Raw Materials Testing
Duration: 2+ years (with likely extensions and/or conversion to permanent)
Posting Date: 3/29/2022
Notes: Candidate will be working on site. Targeting candidates with 4-6 years of industry/ non academia experience and some Capillary electrophoresis experience

3 Key Consulting is hiring a Quality Control Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.

Job Description:
Quality Control Separation Sciences lab is searching is for a team member to support testing for routine, in-process, and stability samples. This person will be responsible for working in the Quality Control laboratory, using GMPs and GDPs to execute analytical testing. The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.

Responsibilities will include, but are not limited to:

Performing analytical testing for CE (capillary electrophoresis, SDS-PAGE, polysorbate extraction and other general chemistry testing.
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.

Why is the Position Open?
Supplement additional workload on team.

Top Must Have Skills:

Capillary Electrophoresis experience a must.
Understanding of quality control and GMP operations.
Team orientated.

Day to Day Responsibilities:

Capillary Electrophoresis experience a must.
Understanding of quality control and GMP operations.
Team orientated.

Basic Qualifications:

4-6 years of experience in capillary electrophoresis.
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.
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.

Employee Value Proposition:
Great biotech/pharma to work for.

Red Flags:
1. Multiple job movement in short time
2. Mistaking SDS-PAGE for CE

Interview process:
Manager interview via Webex
team interview via webex

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.