Senior Director Site Engineering

1 week ago

Fort Lauderdale, United States Teva Pharmaceuticals Full time
Who we are

Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

Leads the Engineering and Maintenance team within the engineering function as the department head and sets both strategic and tactical plans to achieve business objectives of a solid oral dosage facility. The role will lead leaders and technical professional staff supporting the full life cycle of equipment from plan and procure through decommissioning retirement. Will set direction and plans to transition site teams into an autonomous and predictive maintenance organization and develop a multi-year plan and budgets to achieve the goal. Must be able to apply strategic and system based thinking leadership to small teams to drive improvements.

How you'll spend your day

All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments. Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.
  • Ensure availability, reliability, and functionality of production equipment, facilities, and utilities to enable current and future production flow in a safe, quality, and cost effective manner.
  • Carries out managerial responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.
  • Provides guidance and direction to subordinate managers in ensuring compliance with corporate business plans and objectives.
  • Oversees the development and implementation of the Company facility planning process.
  • Formulates and maintains facility environmental and safety objectives complementary to corporate policies and goals.
  • Applies total quality management tools and approaches to production, analytical and reporting processes within each department.
  • Investigates complaints and/or concerns regarding employee safety.
  • Provides facility-planning support to other Company internal customers.
  • Interviews, selects and develops employees; assigns and directs work; conducts performance appraisals and rewards and disciplines employees.
  • Ensures compliance with all Company policies and procedures, including safety rules and regulations.
  • Development of multi-year Capital Plan.
  • Implement Life Cycle Management strategy or Program.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP's), and Standard Operating Procedures (SOP's) instructions.
  • Responsible for performing additional related duties as assigned.
Your experience and qualifications

Education/Certification/Experience:
  • Bachelor's degree in Engineering or a related field from an accredited college or university
  • A minimum 12 years of engineering/management work experience, preferably in a pharmaceutical company
  • Possession of Professional Engineer (P.E.) certification in state of plant operation preferred
  • Six Sigma Black Belt training preferred
  • Solid oral dosage manufacturing equipment knowledge a must (compression, granulation, packaging)
  • Qualification of equipment experience
  • OPEX / Lean implementation experience
  • PMP experience preferred
  • Experience in creating Reliability and Energy Management Program preferred
Skills/Knowledge/Abilities:
  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements
  • Principles and practices of project management, budgeting and contract administration
  • Principles and practices of facility planning, construction and building maintenance
  • Pertinent federal, state and local laws, codes and regulations
  • GMP, SOP, FDA, OSHA and other applicable standards, guidelines and regulatory requirements for pharmaceutical industry
  • Prior experience in a leadership role with both direct and indirect reports managing, directing and coordinating the work of professional, technical and engineering personnel
  • Implementing goals, objectives and practices for effective, efficient and cost effective management of allocated resources
  • Responding to common inquiries or complaints from management, department subordinates, vendors, customers and regulatory agencies
  • Effectively presenting information to top management, public groups and/or boards of directors
  • Interpreting and applying federal, state and local policies, procedures, laws and regulations
  • Communicating clearly and concisely, in English, both orally and in writing
  • Establishing and maintaining cooperative working relations with individuals contacted in the course of work
  • Skill levels in MS Office including proficiency in Word, PowerPoint, Excel and SharePoint
  • Must be able to maintain the highest levels of confidentiality, integrity and discretion


Enjoy a more rewarding choice

We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance.

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva's Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Important notice to Employment Agencies - Please Read Carefully
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

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