192002 - Quality Review
Industry
ENG
Region
FL-Florida
City
Alachua
State
FL
Rate
Up to $60.02 DOE
Duration
5 mos
Description
Chipton-Ross is seeking a Quality Review for an opening in Alachua, FL.

SUMMARY:
The QC Reviewer will work with a team of Scientists and analysts to technically review data, test records and reports generated during testing of GMP clinical lots. The QC Reviewer will communicate status updates on these activities to QC Management, Project Management, and QA to ensure that these activities meet project and production objectives on time.

Occasionally, the role will also support deviation investigations (OOS/OOT, etc) as well as create, revise, edit and prepare QC documents required for the functioning of the analytical GMP QC laboratory. The QC Reviewer will work cohesively with QC Management to ensure consistent delivery and execution of high-quality assay records and laboratory-related documentation.

RESPONSIBILITIES:
Independently perform technical review of data, test records and reports generated during testing of GMP clinical lots. Occasionally assist with creating and revising QC Standard Operating Procedures, Test Records, Stability and Assay Qualification Protocols and Reports. Support deviation investigations (OOS/OOT, etc) that occur within the QC laboratory. Other duties as assigned by supervisor.

REQUIREMENTS:
One to three years of appropriate experience. College coursework may substitute at an equivalent rate for the required experience. Laboratory work experience in the fields of biotechnology, immunology, molecular biology, cell biology, or virology are required for this position. QA or QC experience in analytical testing and development is strongly recommended. Proficiency with Microsoft office programs such as Word, Excel, and PowerPoint. Excellent technical writing and oral communication skills are required. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. Excellent organizational skills. Ability to communicate/work in a high pressure/high paced environment. Ability to multi-task and function effectively as a member of a team.

EDUCATION:
Accredited Bachelor’s degree in Life Sciences, Chemical/Biological Engineering, or an appropriate area of specialization.

WORK HOURS:
Full-Time
M-F 8am-5pm role. Flexibility and overtime may be required on holidays and weekends to support project timelines.

Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.

Contact
Melody Mullins
mmullins@chiptonross.com
CHIPTON-ROSS, INC.
6926 Rivers Ave
North Charleston, SC 29406

Phone: (843) 554-5800 x186 or (800) 927-9318 x186

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.