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Principal Engineer

Job brief

We are seeking a skilled and innovative Principal Manufacturing Engineer to join our dynamic team. The ideal candidate will play a crucial role in optimizing manufacturing processes, improving product quality, and ensuring efficient production operations. This position requires a strong foundation in mechanical engineering principles, along with experience in various engineering tools and methodologies.

Responsibilities

  • Work with suppliers and subject matter experts to identify and implement best industry practices for aseptic manufacturing by developing innovative improvements to safety, processes and production materials
  • Design and complete Engineering studies, proof of concepts and commission reports
  • Support Manufacturing operations by leading technical troubleshooting and improvements
  • Provide technical training to manufacturing and maintenance teams
  • Work in a regulated industry and providing technical reports and work with strong Attention to detail

Requirements

Education/Experience Required

  • Bachelor’s degree in an Engineering related field
  • 8-10 years of experience in a highly regulated environment: pharmaceutical, biotechnology or related industry
  • 5 to 6 years of experience in project management (preferred)
  • Knowledge of FDA and European compliance regulations
  • Knowledge of GAMP guidelines applicable to project management for the pharmaceutical industry.
  • Knowledge of engineering and validation life cycles
  • Experience with various technologies and automated systems used in the pharmaceutical industry
  • Solid “systems” perspective (e.g. understanding implications of project decisions from a holistic perspective).
  • Strong accountability and ownership.
  • Strong leadership and project management skills.
  • Ability to coordinate with different functional areas: Product/Process Development, Tech Ops, Quality and Regulatory groups.
  • Skilled in the practice and application of Lean Manufacturing
  • Skilled in the practice and execution of validation protocols

Skills

  • Autocad or similar CAD platforms
  • Microsoft Office (Word, Excel, Power Point)
  • Microsoft Project
  • Leadership skills
  • Time management skills
  • Math and budgeting skills
  • Analytical skills
  • Strong Written and verbal communication skills and provide technical presentations to various sized groups that simplify the complex
  • Self-Starter
  • Strong analytical skills and ability to troubleshoot utility systems and provide solutions
  • Attention to detail- Accuracy in creating and interpreting detailed drawings and specifications
  • Creative and innovative skills

About STALLERGENES GREER International AG

 

Stallergenes Greer is an international biopharmaceutical company specialized in the research, diagnosis and treatment of respiratory, food and venom allergies through the development and marketing of Allergenic Immunotherapy treatments.

Our mission is to offer the full potential of precision medicine to improve the quality of life of people suffering from allergies.

Allergenic Immunotherapy (AIT) is the only treatment for respiratory allergic diseases that allows for a lasting re-education of the patient’s immune system by inducing an increasing tolerance to allergens.

With more than 1,100 employees worldwide, and production sites in Europe and the United States, Stallergenes Greer offers its medicines in 44 countries.

Would you like to participate in the development of a world expert group in its field, in a dynamic and multicultural environment?

Join our Stallergenes Greer teams!

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