Quality Control Supervisor, Pharmaceutical We are seeking a dedicated Quality Control Supervisor to lead our quality assurance operations within a pharmaceutical setting. This role is pivotal in developing, implementing, and maintaining quality control systems to ensure the precision, accuracy, and reliability of our products. The successful candidate will manage activities aligned with inspecting, testing, and evaluating our product standards to ensure compliance with government and GMP regulations. Salary: $85,000.00 - $100,000.00 per year Essential Duties and Responsibilities: Provide general or direct supervision to a team of exempt and skilled non-exempt employees. Resolve scheduling issues and problems as an advisor and active participant to sub-units within the department. Enforce compliance with data integrity, SOPs, specifications, methods, USP, and cGMP through real-time verifications of records, logbooks, chromatograms, and sequences. Support analysts by troubleshooting methods and instrumentations, as well as executing tests. Schedule the testing and review of raw materials, in-process, finished products, and stability samples, including those from complaint samples and validation activities. Review data critically for anomalies or trends and approve the data, leading and approving investigations into suspect or out-of-specification results and ensuring implementation of CAPA. May perform bench analysis depending on project needs. Interacting with various management levels, both internally and externally, requiring cooperation and presentations on technical projects and schedules. Ensure adherence to all Company, Health, Safety, and Environmental guidelines. Minimum Position Qualifications: BS degree in a scientific discipline with at least 5 years of experience, or an MS degree with 3 years of experience, or equivalent combination of education and experience. Proficiency in MS Word, Excel, and PowerPoint is required. Strong interpersonal and organizational skills. Prior supervisory experience in a relevant field. Preferred Qualifications: Supervisory experience within a pharmaceutical quality control environment. Familiarity with Empower software. Hands-on experience with raw materials and finished product testing. Willingness to relocate to Danbury, CT, with a preference for local candidates. Skills: Ability to lead and manage teams effectively. Expertise in HPLC, raw materials, and finished products analysis. Strong problem-solving capabilities and the ability to manage complex projects. Excellent communication and presentation skills. Benefits: Exceptional benefits package includes 15 PTO days plus 18 paid holidays that include 2 plant shutdowns in July and December. 401K, HSA, and eligibility for an annual bonus. #J-18808-Ljbffr Software Placement Group
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