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Boehringer Ingelheim International - Fremont, CA

posted 2 months ago

Full-time
Fremont, CA
Merchant Wholesalers, Nondurable Goods

About the position

The Associate Engineer, Automation at Boehringer Ingelheim is responsible for maintaining and supporting automation-based systems in a GMP regulated environment, ensuring quality-focused manufacturing of biopharmaceuticals. This role involves collaboration with cross-functional teams to execute automation projects, provide technical support, and optimize automation systems while adhering to compliance standards.

Responsibilities

  • Participate and execute automation-based projects and solutions in collaboration with cross-functional teams.
  • Support the validation of automation systems with qualification and validation functions.
  • Provide technical support to projects in support of the BI Capital Plan.
  • Troubleshoot low to medium complexity issues and investigations.
  • Support automation system hardware and software, including installation.
  • Design automation systems for data integrity, stability, and interface between different systems.
  • Ensure effective maintenance and availability of automation equipment.
  • Implement low to medium complexity automation changes to existing control system hardware and software.
  • Create, modify, and maintain automation system documentation, including specifications and SOPs.
  • Contribute to BPE/MPE activities for continuous optimization processes.
  • Utilize best practices of automation technical standards and procedures locally.
  • Interface with Manufacturing, Process Science, QA, and Contract Engineering/Vendor firms to develop User Requirements and Functional Requirements Specifications.

Requirements

  • High School Diploma with six (6) years of relevant work experience, OR an Associate Degree with four (4) years of relevant work experience, OR a Bachelor's Degree with two (2) years of relevant work experience.
  • Working knowledge of process equipment, instrumentation, and/or computerized systems in biopharmaceutical manufacturing processes.
  • Detail-oriented with excellent written and verbal communication skills.
  • Strong technical writing and presentation skills.
  • Ability to be flexible and manage change.
  • Ability to communicate and collaborate with technical and management staff.
  • Ability to work independently and collaboratively.
  • Strong analytical skills to identify potential improvement opportunities.
  • Good knowledge of economic relations and business needs.
  • Ability to effectively collaborate in multidisciplinary project groups.
  • Good understanding of legal and regulatory aspects within biopharmaceutical business and EHS.

Benefits

  • Competitive compensation and benefit programs
  • Support for a healthy working environment
  • Opportunities for networking and work-life balance
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