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.
Job Description:
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.
Job duties:
Analytical testing of drug substance and drug product.
Basic laboratory stocking/maintenance of equipment.
Position 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)
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
Knowledge & skill requirements
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
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.