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Pharmaceutical Quality Assurance Specialist

Company: crox
Location: Summit
Posted on: November 26, 2022

Job Description:

Position: - Manufacturing QA Analyst/ SpecialistLocation: - Summit, NJ 07901Job Type: - Long Term Contract opportunity REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: Must have sound knowledge and experience in FDA regulated cGMP Quality Manufacturing operations and processes. Directs quality initiatives that accomplish continuous improvement and enhance site quality system efficiencies. Must be action-oriented and customer-focused and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking. Must possess an independent mindset. Requires moderate direction to complete more complex tasks; completes routine tasks with little or no supervision. Work is self-directed. Confident in making decisions for non-routine issues. Routinely recognizes and resolves Quality issues; Informs management of proposed solutions. Seeks management guidance on complex issues. Develops procedures. Proposes solutions for complex issues and works with management to resolve. Follows established procedures and performs work as assigned. Intermediate to advanced ability to interpret results and situations and articulate recommendations for resolution. Must be action-oriented and customer-focused and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking. Understands continuous improvement and improves efficiency and productivity within the group or project. Builds relationships internally within and with cross functional teams. Contributes to goals within the work group. Able to recognize conflict and notify management with proposed recommendations for resolution. Able to prepare written communications and communicate problems to management with clarity and accuracy. Able to effectively multi-task. Knowledge of US and global cGMP requirements. Excellent verbal and written communication skills. DUTIES AND RESPONSIBILITIES: Build and maintain relationships with Manufacturing Operations, Quality Control, Manufacturing Science & Technology and other departments to effectively accomplish responsibilities make improvements and resolve issues. Ensure manufacturing compliance with applicable procedures and batch records. Perform real time review of manufacturing batch records. Review manufacturing shop floor documentation. Issue production batch records and product labels to Operations. Must have strong authorship and ability to critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles. Must be skilled in planning and organizing, decision-making, and building relationships. Knowledge of quality processes, including material disposition, change control, product complaints, deviations, investigations, and CAPA management. Must be able to work in the cleanroom environment for 6-hour time periods. Must be available for weekend and off-shift hours. Must be flexible for shift hour changes to support manufacturing. EDUCATION AND EXPERIENCE: Minimum high school diploma required, with equivalent experience. Bachelors degree with 4+ years of relevant work experience preferred Aseptic experience preferred, but not required.Job Type: ContractSalary: $30.00 - $35.00 per hourSchedule: 8 hour shift Monday to FridayEducation: Bachelor's (Preferred)Experience: CGMP: 4 years (Required) Quality assurance: 4 years (Required) Pharmaceutical Industry: 4 years (Required)Work Location: One location Speak with the employer

Keywords: crox, New York , Pharmaceutical Quality Assurance Specialist, Healthcare , Summit, New York

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