Description:
Note:
Fully Onsite - 8-5 (Flexible)
Ideal Candidate: 1-2 years of experience in a GMP setting + a B.S. Please review the top 3 skillsets.

Job Details: Under general supervision, this position will perform routine procedures to support drug substance and drug product testing within Quality Control. Tasks may include but are not limited to performing sample collection, sample handling, testing equipment/laboratory support. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Documenting, computing, compiling, interpreting, and entering data into computerized systems- Maintaining and operating specialized equipment - Initiating and /or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks.

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

Experience:
Master's degree OR Bachelor’s degree and 1-2 years of Quality or Analytical Laboratory experience OR Associate's degree and 3-5 years of Quality or Analytical Laboratory experience OR
High school diploma/GED and ?5 years of Quality or Analytical Laboratory experience

Preferred Qualifications

• Experience in GMP analytical laboratory
• Experience with HPLC/UPLC, general chemistry, capillary electrophoresis
• 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.
• 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.
• Demonstrated experience in investigations and QC processes

Basic Qualifications    
High school/GED + 4 years work experience or Associate + 2 years work experience or Bachelor + 6 months work experience or Masters Degree

Top 3 Must Have Skill Sets:    

• General Chemistry/HPLC/Capillary Electrophoresis experience in a GMP setting
• Quality Control experience in a GMP setting
• Ability to manage time well and adapt to a fast paced, dynamic environment
• Strong communication and collaborative skills
• Nice to have: Empower and LIMS knowledge.

Pay Rate $21 to $24 on W2 based on experience.

"This posting is for Contingent Worker, not an FTE"