Job Title: Quality Control Senior Associate – (JP9399) Location: West Greenwich, RI. Employment Type: Contract Business Unit: ARI Quality Control Duration: 1+ years (with likely extensions and/or conversion to permanent) Posting Date: 11/3/2021
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: Onsite. Candidate needs industry experience. This is not an entry-level position, therefore someone straight from college would not be suitable even if they have an advanced degree.
Quality Control Bioanalytics is searching is for an analytical scientist to support testing for routine and stability samples for multiple drug substance programs. 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. Responsibilities will include, but are not limited to:
Performing analytical testing and review for HPLC/UPLC and UV assays.
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.
What we are looking for:
Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.
Demonstrated ability to work independently and deliver right first time results.
Excellent communication skills (written and verbal).
Must have focus on data integrity.
Qualified to work in the U.S. without employer sponsorship.
Commitment of a 40-hour work week in West Greenwich, RI.
Why is the Position Open? Supplement additional workload on team.
Top Must Have Skills:
•Strong Analytical Skills – Ideal candidate will have at least 4 years of experience performing analytical testing
•Attention to Detail – Ideal candidate will be thorough and deliver polished work product.
•Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to participate in lean initiatives on site.
Day to Day Responsibilities: Daily responsibilities will be focused on executing analytical testing utilizing HPLC/UPLC (Agilent and Waters Instruments) and Protein Concentration UV testing in a GMP laboratory.
Basic Qualifications: Master’s degree OR Bachelor’s degree + 2-4 years of directly related experience OR Associate's degree and 6 years of Quality or Analytical Laboratory experience OR High school diploma/GED and 8 years of Quality or Analytical Laboratory experience
Employee Value Proposition: Opportunity for growth and exposure to a large bitotech environment.
Red Flags: Must have industry experience. No one straight from college even if they have an advanced degree
Video Skype Panel Interview
We invite qualified candidates to send your resume to firstname.lastname@example.org. 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.