Principal Device Engineer
| Company | Pfizer |
|---|---|
| Location | Parsippany-Troy Hills, NJ, USA |
| Salary | $96300 – $160500 |
| Type | Full-Time |
| Degrees | Bachelor’s, Master’s, PhD, Associate’s |
| Experience Level | Senior, Expert or higher |
Requirements
- Applicant must have a High School Diploma (or Equivalent) and 10 years of relevant experience OR an associates degree with 8 years of experience OR a bachelors degree with at least 5 years of experience OR Masters Degree with more than 3 years of experience, OR a PhD with 0+ years of experience.
- Demonstrated experience in product development, manufacturing science and technology, sterilization or process validation or Process Engineering within the pharmaceutical industry
- Thorough knowledge of cGMP (current Good Manufacturing Practices), combination device regulations, design control
- Strong history of problem solving skills, project and task management skills, ability to manage priorities and lead others under pressure
- Strong verbal and written presentation communication skills and attention to detail
Responsibilities
- Provide testing and technical support for all new facilities and new processes in manufacturing.
- Support of process and component improvements projects as needed.
- Evaluate, manage, and report the process capability of the equipment and services employed in the operation.
- Manage supplier technical audits and Pfizer corporate audits.
- Actively share knowledge with others within the team through existing knowledge sharing processes and systems.
- Apply technical knowledge of Operations, Quality, Validation, etc. along with internal/external business challenges to provide input into recommendations for improvements.
- Lead multi-functional project teams through high technical risk assessments and complex engineering/technology solution development.
Preferred Qualifications
- Relevant pharmaceutical experience