- 205644 - QC Scientist I
- $23 to $25.00 DOE
- 12 Months
- Chipton-Ross is seeking a QC Scientist I for a contract opportunity in Cincinnati, OH.
The QC Scientist I performs routine analyses and documentation of any of the following: Raw Materials, In-Process, Finished Product, Calibrations, Stability samples or projects within the QC Chemistry Laboratory, in a manner consistent with established standards. Supports internal development and/or manufacturing operations. Makes detailed observations & reviews, documents, and communicates test results.
Conducts routine chemical & physical testing of raw materials, finished products, and stability samples by internally developed and compendial test methods. Performs validated test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, and characteristics by using HPLC, GC, dissolution, spectroscopy, and/or traditional wet chemical testing.
Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems effectively & efficiently. Performs daily instrument calibrations/verifications as the need arises. Clearly and accurately communicates the results of work by accurate documentation of the testing/analysis & acquired results.
Records and reports results of analysis in accordance with prescribed lab procedures & systems.
Prepares test solutions including diluents and mobile phases.
Cleans and maintains work area & instrumentation. Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintains vital compliance status required by company and facility standards.
Experience performing chemical tests with chromatographic, spectroscopic, or other analytical technique preferred.
Equivalent combinations of education, training, & meaningful work experience may be considered.
Good knowledge & understanding of basic instrumental technologies and qualitative & quantitative chemical analyses.
Awareness of quality & regulatory requirements in the pharmaceutical industry.
Good problem-solving skills and logical approach to solving scientific problems.
Follow all company policies, SOPs, cGMPs, work instructions, methods & analyst guidelines.
Demonstrates efficiency by multitasking and scheduling time to meet required workload.
Actively seek additional assignments when testing in primary area of responsibility is completed.
Takes initiative and independently pursues training and/or learning opportunities to improve personal skills and share skills with other team members.
Shown interpersonal and communication skills (both oral & written).
Ability to read and interpret technical procedures and governmental regulations.
Ability to apply mathematical operations to such tasks as determination of test reliability, analysis of variance, and correlation techniques.
Ability to work in a fast-paced environment.
Bachelor’s degree, or greater, in physical science, preferably in Chemistry or Biology.
WORK HOURS: Full-Time.
Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.
420 Culver Boulevard
Playa Del Rey, CA 90293
Phone: (310) 414-7800 x307 or (800) 927-9318 x307
Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.
Employment will be contingent on candidate clearing pre-employment drug screen and background check.
Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.