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Quality Control Scientist I

3 months ago

Cincinnati, United States Chipton-Ross Full time

Chipton-Ross is seeking a Quality Control Scientist I for a contract opportunity in Cincinnati, OH.

SUMMARY:
The Quality Control Scientist I performs routine analyses and documentation of any of the following: In-Process and Finished Product samples for pharmaceutical batch Release, 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.

RESPONSIBILITIES:
o Conducts routine chemical testing of finished products, and stability samples by internally developed and compendial test methods.
o Performs validated test methods for pharmaceutical finished products for strength, impurities, identity, and characteristics by using HPLC and wet chemistry techniques.
o Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems efficiently.
o Performs daily instrument calibrations/verifications as required.
o Clearly and accurately communicates the results of work by accurate documentation of the testing/analysis & acquired results.
o Records and reports results of analysis in accordance with prescribed lab procedures & systems.
o Prepares test solutions including diluents and mobile phases.
o Cleans and maintains work area & instrumentation
o Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.
o Maintains vital compliance status required by company and facility standards.

REQUIRED EXPERIENCE:
o 1-2 years of experience performing chemical tests with chromatographic technique is preferred.
o Working theoretical knowledge of HPLC is required as well as practical execution.
o Equivalent combinations of education, training, & meaningful work experience may be considered.
o Good knowledge & understanding of basic instrumental technologies and qualitative & quantitative chemical analyses.
o Awareness of quality & regulatory requirements in the pharmaceutical industry.
o Good problem-solving skills and logical approach to solving scientific problems.
o Follow all company policies, SOPs, cGMPs, work instructions, methods & analyst guidelines.
o Demonstrates efficiency by multitasking and scheduling time to meet required workload. Actively seek additional assignments when testing in primary area of responsibility is completed.
o Takes initiative and independently pursues training and/or learning opportunities to improve personal skills and share skills with other team members.
o Shown interpersonal and communication skills (both oral & written).
o Ability to apply mathematical operations to such tasks as determination of test reliability, analysis of variance, and correlation techniques.
o Ability to work in a fast-paced environment.

PHYSICAL REQUIREMENTS:
Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Use of:
o Safety glasses
o Safety shoes
o Lab coat
o Latex or similar gloves
o Safety apron
o Organic respirator occasionally (i.e. Surge 100)

EDUCATION:
Accredited Bachelor's degree, or greater, in physical science, preferably in Chemistry.

WORK HOURS:
Full-Time; Mon-Friday