QA Specialist
KBI BioPharma
Biopharmaceutical Development Gmp Compliance ReviewerThis position is responsible for the compliance review of Biopharmaceutical Development GMP data. This includes the review and approval of release, in-process, and stability test data. This position is also responsible for the review and approval of method qualifications and validations. Another responsibility is the review and approval of laboratory investigations and deviations associated with the biopharmaceutical development department.Job Responsibilities:Performs compliance review on the following records: release, in-process, and stability data.Responsible for the review and approval of method qualifications and validationsResponsible for the review and approval of deviations and laboratory investigations.Minimum Requirements:BS and 11+ years experience or MS and 8+ years experience in a CGMP regulated environment within biopharmaceuticals or equivalent.Experience in QA review of analytical data (release, in-process, and stability), experience in reviewing method qualifications/validations and the review and approval of laboratory investigations and deviations. Knowledge of USP, EU and JP cGMP guidelines.Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.Basic math skills are required.Ability to apply concepts of basic algebra and statistics.Be able to sit for long periods of time.Ability to lift 20 pounds.Ability to use word processing, database, spreadsheets, power point, internet, e-mail, calendar, computer, telephone
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$43.08 - $80 per hour
Summary Quality is not just a checkpoint here—it is the promise we make to patients. As a Manufacturing Quality Assurance Specialist at Novartis, you will be a hands-on partner to manufacturing teams, ensuring every stage of production meets the highest...Hourly payRelocation packageMonday to FridayShift workDay shift- ...experienceAbout the roleThis position is responsible for providing QA oversight and auditing of activities related to clinical and... ...Management.About youEducation/ Qualifications:· Quality Assurance Specialist - Bachelor’s degree, in a health care or relevant scientific...Flexible hours
$138.6k - $257.4k
Job Description SummaryJoin Novartis as our QA Operations Head and play a pivotal role in ensuring patients receive high-quality medicines that meet the highest standards of safety, compliance, and reliability. This is an opportunity to lead a critical Quality Operations...Full time- ...immediate contract by leveraging your skills to ensure products meet regulatory and internal standards. This role is ideal for experienced QA workers seeking project variety and immediate opportunity.Your responsibilities:Compliance auditing: perform process audits and...Contract workTemporary workImmediate start
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- ...immediate contract by leveraging your skills to ensure products meet regulatory and internal standards. This role is ideal for experienced QA workers seeking project variety and immediate opportunity. Your responsibilities: - Compliance auditing: perform process audits...Contract workTemporary workWork experience placementImmediate start
$89.6k - $166.4k
...#LI-Onsite Location: Morrisville, North Carolina The QC Specialist II is a highly skilled laboratory professional who will support... ...requirements, and Novartis policies while collaborating across QA, QC, MS&T, Engineering, Operations, and other site functions....Work experience placement
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