Quality Control Senior Associate JP

Position: Quality Control Senior Associate - (JP10451)
Location: West Greenwich
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 sendyour resume  Ifyou decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our  You are also welcome to sharethis opportunity with anyone you think might be interested in applying for this role.

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