Valeant Pharmaceuticals

  • Team Leader, Aseptic Prep-3rd Shift

    Location US-FL-Tampa
    Job ID
    10360
    Category
    Operations
    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 provide leadership in the Aseptic Prep Department for all personnel to ensure that quality products are manufactured to meet the production plan. Place customer service and accountability to the customer as the constant goal. Coordinate closely with other departments on operational and planning issues related to meeting the production plans and company goals. Assume responsibility for the GMP, environmental health and safety procedure awareness and compliance within the respective area.

     

    This position is from Tuesday to Saturday. Hours are 11:00pm-7:30am. 

     

    This position will supervise direct reports. 

    Responsibilities

    • Supervise, develop, provide feedback and coach employees. Complete performance reviews semi-annually.
    • Review weekly production schedule and work with the Planning department on capacity and scheduling issues. Coordinate activities to support the production schedule. Participate in process related issues using thorough technical process knowledge.
    • Perform investigations and write reports as required.
    • Review, approve, write and revise SOP's and other documentation.
    • Participate and lead in Operational Excellence projects and attend GMP training sessions as required. Train/re-train department personnel on safety, cGMPs and SOPs as needed. Work with Tech Services, R&D and Contract Manufacturing on the transfer of new products & engineering studies. Perform audits of area on scheduled basis for compliance to procedures.
    • Asset and supply management. Generate required WOs and POs. Operate department within budget guidelines. Review standards annually for necessary revisions.

    Qualifications

    • BS in Science/Technical field; Chemistry, Biology or Engineering. Can be augmented with years of experience in sterile pharmaceuticals.
    • Demonstrated exceptional people management and leadership skills.
    • Detail oriented.
    • Makes decisions based on reason and data.
    • Problem solving, facilitator and management skills.
    • Self-initiative.
    • Exceptional communication and documentation skills.
    • Demonstrated analytical skills.
    • Must be results oriented on a continual basis

     

    Valeant Pharmaceuticals International, Inc. is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

    Be Aware of Recruiting Fraud

    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