30 days old

Engineering Projects Manager

Irvine, CA 92606

Company Info

 

If youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.


Tevas Irvine, CA production site is one of our complex manufacturing and supply chain operations.


We are strengthening and adding to our critical teams with great talent and capabilities. Teva, a global organization, with a brand of evolving success.  Be part of it!

 

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, 6% match on the 401(k), Employee Stock Purchase Plan and Tuition Assistance

 

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

 

Teva is searching for an Engineering Manager to join our team in Irvine, CA!

 

This position will be filled by an individual who possesses the knowledge, background and skills to successfully support all technical issues associated with a pharmaceutical manufacturing facility. This includes the ability to collaborate with all levels of management and coordinate projects with outside vendors and suppliers while performing and managing multiple tasks on a daily basis ensuring the most cost effective and productive methods are utilized to support and maintain facilities and equipment for a GMP pharmaceutical manufacturing facility. 

 

You will:

  • Write Capital Expenditure Requests (CER) for the engineering department, and assist other departments in writing CERs. Ensure that all capital projects include BOD, URS, EHS Review, Risk analysis, Commissioning plans, and Schedule as required per project. Interface with procurement for Purchase Orders (POs), Update, and write Blanket Purchase Orders (BPOs) as needed. Write technical CER POs as needed for engineering verbiage.
  • Oversee Capital Project budgets for the site.  Meet corporate reporting requirements for capital projects, to include CAPEX justifications, cash flow tracking and reporting.  Track Capital spending, PO status, delivery schedules and project status in a central location that is accessible to the site.  Help administrative assistants enter technical POs.  Ensure that capital package is complete before it is executed.
  • Provide technical engineering expertise on projects as needed, including interfacing with outside Engineering firms for project support, managing Contract Engineers and outside vendors on assigned projects.  Participate in the design and detailed engineering of a new or remodel of an existing facility.  
  • Commission and qualify facility or equipment systems installed or modified for Capital or other projects.  Perform periodic updates to qualifications of existing systems as needed. 
  • Generate TrackWise change controls for on-boarding or modifying equipment or facilities.  Support TrackWise events and CAPAs as needed.
  • Maintain and update the GMP and non-GMP drawings for the facility and maintain and update the equipment tracking list.
  • Complete all training requirements and maintaining 100% compliance with all assignments.  
  • Maintain work areas and perform job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs) and Batch Record instructions.

Qualifications

 

  • Requires a Bachelors Degree in Engineering.
  • Requires 7+ years of experience in engineering and construction.
  • Prefer 3+ years of pharmaceutical manufacturing experience.
  • Project Management experience with Project delivery experience of $100K to $3MM budget including capital projects strongly preferred.
  • Demonstrated experience installing critical machinery and automation equipment in GxP environment.
  • Ability to work independently and collaboratively and manage stakeholders at all levels.
  • Capable of identifying related work scopes, identification of process steps, resource skills required and accurate estimation of timelines.
  • Sound contractor management skills.
  • Thorough, detail-oriented and a good communicator.
  • Demonstrate flexibility and work well in a fast-paced environment.
  • A desire to innovate and improve processes and demonstrated experience driving lean concepts in design and execution.
  • Strong adherence to compliance and safety requirements, cGMPs, SOPs, and other manufacturing documents.
  • Ability to be customer-focused, self-driven and comfortable with ambiguity and complex problem solving. Able to quickly prioritize work in alignment with business and customer needs.
  • Team-oriented with a passion for continuous improvement.
  • Excellent verbal and written communication skills required.
  • PMP certification preferred.
  • Experience in Sterile pharma industry preferred.

Function

Engineering

Sub Function

Engineering

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 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. 

Categories

Posted: 2021-03-11 Expires: 2021-04-28

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Engineering Projects Manager

Teva Pharmaceuticals
Irvine, CA 92606

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