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MES Engineer

Date: Nov 25, 2022

Location: Buenos Aires, AR, B1652

Company: Teva Pharmaceuticals

Who are we?

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

 

Job title: MES Engineer

Purpose:  Responsible for the conversion of Master Batch Records (MBRs) into electronic format. To be part of MES-related activities including: testing / validation, change control, process improvement and troubleshooting. This position also serves as the internal point for SAP implementation in the company.

Key Responsibilities:

  1. Internal point for SAP implementation.
  2. Responsible for performing conversion of Master Batch Record (MBR) documents to the Electronic Batch Record format for use in the Manufacturing Execution System (MES).
  3. Responsible for overseeing the installation and performing qualification of shop-floor hardware to support MES and other data collection systems (SCADA).
  4. Responsible for performing periodic reviews of computer systems and system qualifications, preparing summary reports, and assigning CAPAs to address deficiencies.
  5. Responsible for collaborating with other functional areas of the organization such as Manufacturing, Quality, and Supply Chain to accomplish project objectives.
  6. 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), Standard Operating Procedures (SOP’s) and Batch Record instructions.

Qualifications

Academic Background: Bachelor’s degree in Engineering or related field such as Industrial Engineering, Manufacturing Engineering, Operations Management, Information Systems, Computer Science, or similar

Experience: 3 years in manufacturing environment, ERP implementations and desirable understanding of pharmacological compliance, legal and industry standards.

Technical Knowledge: Computer proficiency with comprehensive working knowledge of MS Office products, SAP, MBRs, MES, SQL, LIMS, Trackwise, Livelink and Qdocs.

Language: Advanced English

Competences:

  • Communication
  • Organize and Prioritize
  • Proactive
  • Analyze workflows

Function

Engineering

Sub Function

Equipment Maintenance Technical Specialty

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.