Apply to Quality Control Senior Associate - (JP10451)

Job Title: Quality Control Senior Associate - (JP10451)
Location: West Greenwich, RI. 02817
Employment Type: Contract
Business Unit: ARI QC Bioanalytics
Duration: 2+ years (with likely extensions)
Posting Date: 06/20/22
Notes: Only qualified candidates, please. 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 an 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.

Basic Qualifications:

4-6 years of experience in capillary electrophoresis and/or quality control setting
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.

Top Must-Have Skill Sets:

Capillary Electrophorese and/or Empower experience preferred

Teamwork and collaborative mind set
Must have Quality Control lab experience and understanding of GMP expectations
HPLC and UPLC experience

Day to Day Responsibilities:

Routine and non-routine testing
Maintain training
maintain laboratory workspace
Review documents

Red Flags:

R&D experience only
Frequent job changes

Interview process:
Video conference call (webex) with manager and/or potential team member
Second interview with team if required (webex)

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.