What are the responsibilities and job description for the Senior Quality Control Associate position at US Tech Solutions?
Job Title: Quality Control Senior Associate
Duration: 12 months contract
Location: West Greenwich, RI
Must Have Skills:
- 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.
About the Job:
As a Quality Control Senior Associate, you will perform routine procedures to support drug substance and drug product testing within Quality Control. Your tasks may include sample collection, sample handling, testing equipment/laboratory support. You 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
Key Responsibilities:
- Analytical testing of drug substance and drug product
- Basis laboratory stocking/maintenance of equipment
Requirements:
- 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)
- Focused on data integrity
- Qualified to work in the U.S. without employer sponsorship
- Commitment of a 40-hour work week in West Greenwich, RI
Desirable Skills:
- 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
