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QC Scientist
Career Insights for Quality Control Analyst
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Based on Pennsylvania data
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What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$67,403 / year median in Pennsylvania
-16% projected decline
Job Description
Job ID:
10367819 Posted today Back Lititz, PA, US Scientific Bachelors Degree Full Time, Temporary 32-38 Entry Level On-site Personal Care and Cosmetics Second Shift (Afternoon) Lititz, PA, US 32-38 Entry Level Full Time, Temporary Personal Care and Cosmetics On-site Scientific Bachelors Degree Second Shift (Afternoon) Apply Now Applied Job details QC Scientist Every day, Kelly Science & Clinical connects professionals with opportunities to advance their careers. We currently have exciting temporary opportunity as a QC Scientist with a global leader in the production of consumer products and pharmaceuticals inLititz, PA Location:
Lititz, PA Contract:
1 year, possible extensionSchedule:
M-F, 2nd Shift (2PM-10:30PM)Compensation :
$32-38/hrSummary :
The Quality Control Scientist I is an entry level analyst responsible for performing a variety of analytical testing (raw material, in-process, finished product, and stability) and non-testing activities with moderate supervision to support the analytical laboratory. This position is responsible but not limited to the following: capable of basic bench wet and physical chemistry testing, analytical assay testing through chromatography analysis (such as but not limited to UPLC, LC, GC, IC, and UV), peer review (review of standard and reagents), assisting in the upkeep and revisions of laboratory documents (test notes, SOPs, Work Instructions, and Job Aids), and additional tasks as needed. Responsibilities Follow all required procedures (SOP, Kenvue Test Methods, Product Specifications, Raw Material Specifications, Test Notes, and Pharmacopoeia Test Methods) Perform basic wet bench testing and physical testing Perform Chromatography Analyses Participate as needed with laboratory and non-conformance Investigations Peer Review of Standard and Reagents Capable of learning new testing techniques Able to troubleshoot instrument and testing issues. Document upkeep support (updating as needed SOPs, Test Notes, Job Aids, and Work Instructions) Participate in the labs 5S program Proved assistance/lead non-testing projects that is designed to benefit the QC laboratory in process improvements and efficiency gains Good documentation skills - following GLP practices and laboratory procedures Remain compliant by completing on-time required trainings Qualifications BS in the Scientific field 0-2yrs of industry experience undergraduate research/internships/co-ops considered in lieu of industry experience1-3yrs of experience Knowledge of GMPs and good documentation practices strongly preferred Good Communication Skills Knowledge of Basic Chemistry, able to work in a team environment, work under GMP requirements required P#1 Important information: This position is recruited for by a remote Kelly office, not your local Kelly branch. Must be legally permitted to work in the United States.Send resumes to:
Jacqueline.Sayoc@KellyScientific.com 10367819 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.