Position Title: Senior Quality Control Associate
Work Location: West Greenwich, RI 02817
Assignment Duration: 12 months (Possible Extension)
Work Schedule: Fully Onsite - 8-5 (Flexible)
Work Arrangement: Onsite
 
Position Summary:

• Perform routine procedures to support drug substance and drug product testing within Quality Control.

 
Background & Context:

• The ideal candidate will have 1–2 years of hands-on experience in a GMP-regulated lab, with strong proficiency in HPLC, capillary electrophoresis, and general chemistry testing (e.g., pH, osmolality, sub-visible particles).
• They must be able to troubleshoot lab instrumentation, demonstrate a strong sense of data integrity, and clearly articulate their role within a team.
• Candidates without GMP experience or with solely academic/microbiology backgrounds will not be considered.
• The team requires someone who can quickly contribute with minimal training. Please no Microbiology candidates they are not fit for the role.

 
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 in GMP analytical laboratory.
• Experience with HPLC/UPLC, general chemistry, capillary electrophoresis
• Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.
• Must have focus on data integrity

 
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

• Ability to work independently and deliver right first time results
• Excellent communication skills (written and verbal)
• 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

 

 


At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $35.00/hr.