Quality Assurance Specialist in Summit, NJ at Pyramid Consulting, Inc

Date Posted: 11/27/2019

Job Snapshot

Job Description

Immediate need for a Quality Assurance Specialist  experience in the Pharmaceutical Industry. This is 12+ Months Contract position with possible extension located in Summit, NJ. Please review the job description below:

JOB ID # 19-47858

Attn: the training process will be normal business hours Please note this may require shift work meaning nights and or weekendsREQUIRED COMPETENCIES:• Must have advanced knowledge and experience with cGMP manufacturing, Quality, and compliance.• 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.Responsibilities:• Perform QA shop floor activities.• 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.• Able to effectively multi-task.This position will provide 12 hour coverage including nights/ weekends.

Our client is a leading Pharmaceutical Organization and we are currently interviewing to fill this and other similar Contract positions. Qualified candidates should apply online for immediate consideration.
 
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