Teva Pharmaceuticals USA, Inc.

Manufacturing Engineer II

US-UT-Salt Lake City
Requisition #
17-20157
# Positions
1
Category
Operations - Maintenance

Overview

Under general supervision, assists in troubleshooting the manufacturing and packaging areas. Provides technical support to all departments in the areas of equipment operation and process improvements.

Responsibilities

  • Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws.
  • Provides assistance in troubleshooting and identification of equipment problems. A daily presence on the plant floor is required to understand the proper operation of equipment as well as being able to identify the incorrect operation of equipment.
  • Maintains relationship with operators as well as maintenance mechanics to foster a good team environment when working on the equipment.
  • Writes SOP’s and other technical documents in support of the engineering department as well as the end users.
  • Assists in the execution and design of qualification protocols. Requires an understanding and working knowledge of the equipment so that the appropriate testing is created to guarantee the operation of the equipment in a GMP environment. Processing needs and equipment specifications must be analyzed and interpreted to create appropriate tests.
  • Helps specify and procure equipment for new projects.
  • Complies with all Company policies and procedures, including safety rules and regulations.
  • Performs related duties as assigned.

Qualifications

Knowledge of:

  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements in a regulated manufacturing environment.
  • OSHA, FDA, EPA, AQMD and other applicable regulatory and safety compliance guidelines.
  • Dry and wet blend granulation’s, including fluid bed granulates, high shear granulators, blenders, mills, multiple tablet presses, and tablet coaters.
  • Packaging equipment systems, such as vibratory fillers, slat fillers, cappers and labelers.
  • Manufacturing process engineering principles and practices.
  • Engineering and business computer hardware and software.
  • English usage, spelling, grammar and punctuation.
  • Company safety rules and regulations, worker's compensation and related practices.

Skill In:

  • Performing necessary engineering projects and assignments in a cost effective and timely manner.
  • Ensuring compliance with all Company policies and procedures, including safety rules and regulations.
  • Analyzing and troubleshooting problems, identifying solutions, and recommending and implementing methods, procedures, systems and/or techniques for resolution.
  • Functioning as an individual contributor, with little or no supervision.
  • Ensuring compliance with all Company policies and procedures, including safety rules and regulations.
  • Operating a personal computer and standard office applications including word processing.
  • Reading, writing and speaking English.
  • Communicating clearly and concisely, both orally and in writing.

Minimum Qualifications:

Bachelor’s degree in engineering or a related field from an accredited college or university and five (5) or more years of process engineering experience, preferably in pharmaceutical, food, or cosmetic manufacturing environment; or an equivalent combination of training and experience.

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