Location: Danbury,CT, USA
Pharmaceutical Quality Control SupervisorApplyLocation Danbury, CTType Direct HireID CA168-#######Pharmaceutical Quality Control SupervisorDanbury, CT$85,000 to $100,000 + Full Benefits + Paid RelocationJob SummaryDevelops, implements and maintains the activities of quality control systems. Oversees methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products. Contributes information to help develop budgets. Makes recommendations for corrective action necessary to assure conformity with quality specifications. Assures finished products conform to government and company standards and satisfies GMP regulations.Essential duties and key job responsibilities and essential functions.Provide general or direct supervision to exempt employees and/or skilled nonexempt employeesAct as advisor to unit or sub-units, becomes actively involved as required to meet schedules or resolve problemsProvides supervision on the floor enforcing compliance data integrity, SOPs, specifications, methods, USP, and cGMP through real time verifications of records, logbook, chromatograms, sequences, etc.Helps analysts by trouble shooting methods, instrumentation and execution of the tests.Schedules testing/review of raw materials, in-process, finished product, and stability samples, complaint samples, samples from process and cleaning validation activitiesExercise judgment within defined procedures and policies to determine appropriate action. Critically review data for anomalies or trends and approve dataLead and approve investigations of suspect or out of specification results. Ensures implementation of CAPA.May perform bench analysis, as neededFrequently interacts with subordinates, outside customers, and functional peer groups at various management levelsInteraction normally requires the ability to gain cooperation of others, conducting presentations of technical information concerning specific projects/schedules, etc. Contributes to cross functional projects with significant impact to companyResponsible for observing all Company, Health, Safety and Environmental guidelinesDuties and responsibilities are not limited to the work listed above and may include other assignments as necessaryAs a member of the Quality organization the incumbent is also expected to use quantitative reasoning; and to be professional, committed to excellence, customer focused, detail oriented, a communicator, and a team player.(Where reference is made to regulatory environment requirements and/or compliance this includes all applicable regulations i.e. FDA, ISO 13485/9001, European requirements, etc.)Section III: Minimum qualifications to perform the job; specific skills, education, knowledge and job experience necessary to perform essential duties; physical requirements for job if any. BS degree in a scientific discipline with 5+ years' experience or MS with 3+ years of experience or a combination of experience and trainingProficiency in MS Word, Excel, and PowerPointStrong interpersonal and organizational skillsSupervisory experienceSkills and Certifications Supervisory ExperienceHPLCFinished ProductsEmpowerIdeal Candidate Looking for candidates that have worked in Pharmaceutical in Quality Control with supervisory experience.Familiar with Empower software. Raw materials and finished products.Must be willing to relocate to Danbury Ct.Local candidates are preferred.No H1Bs or TN visas.Exceptional benefits include 15 PTO days plus 18 paid holidays that include 2 plant shutdowns (July and December).#J-18808-Ljbffr