Valeant Pharmaceuticals

  • Senior QA Supervisor, Training

    Job Location US-FL-Tampa
    Job ID
    10204
    Pos. Category
    Quality
    Pos. Type
    Full Time
  • Overview

    Valeant Pharmaceuticals International, Inc. is a diverse pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.

     

    This position will be responsible for the continuous development and maintenance of Quality Systems at the B& L Tampa Pharmaceuticals Organization. Mentor, coordinate and manage that Training team to ensure that site Training requirements are met.

     

    This position will supervise staff that develops and delivers training support to the site. Work with cross-functional teams to develop/improve Quality Systems. Develop and improve training materials associated with onboarding, reducing human error, line release/clearance, Good Documentation Practices etc. 

     

    Oversee the Administration of the ComplianceWire Learning Management and the System Administrator Training functions, including user access, workflows for organizing users and managing curriculums / user groups / assignments.

    Responsibilities

    • Supervise staff in connection with developing and delivering training materials
    • Performs a wide variety of activities to ensure Quality System compliance with applicable quality objectives and regulatory requirements.
    • Manages GMP Trainers / LMS Administrators.
    • Designs, develops and delivers high quality and high impact learning products, programs and services that provide functional, GXP and product knowledge for staff to achieve a high level of performance in their jobs.
    • Evaluates the effectiveness of site Quality Systems and training, monitors training compliance for staff.
    • Collaborates with Senior Management teams to ensure optimal tracking of training records and training compliance.
    • Maintains the GXP Training program and processes to ensure compliance with current GXPs.
    • Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
    • Responsibilities also include interviewing, hiring, terminating and training employees; planning, assigning, and directing work; appraising performance; counseling employees; and conflict resolution.
    • Keeps abreast of the requirements for compliance in area of responsibility. Participates as required in training on regulatory issues affecting own area of work. Notifies manager of regulatory compliance questions and issues.

    Qualifications

    • Minimum of BA/BS
    • Supervisory leadership and training experience
    • High level of competency of MS office applications such as MS Word, Excel and Access
    • 5+ years of experience in Training Compliance in a Pharmaceutical Manufacturing GMP Environment or equivalent.
    • Adept with presentation skills to deliver broad material to an audience.
    • Experience in the administration of ComplianceWire is strongly preferred
    • Experience with other Quality Systems a plus.

    Be Aware of Recruiting Fraud

    Valeant is an EEO/AA employer M/F/D/V.

     

    Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

     

    To learn more please read Valeant’s Job Offer Fraud Statement.

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed