- Bachelor's degree
- Master's degree
Why Patients Need You
Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action.
Provides technical expertise and operational support for Drug Product Operations and specifically the new Modular Aseptic Processing (MAP) facility. Partners with shop floor colleagues and supervision to ensure smooth and efficient production of a diverse mix of products. Assists in equipment troubleshooting activities as needed. Serves as a subject matter expert within the site for highly automated aseptic preparation, formulation, filling, isolator, or lyophilization systems. Responsible for technical development of junior colleagues.
Identifies and implements cost savings ideas, specifically efficiency improvements and other projects that increase equipment capacity.
Develops and validates manufacturing processes for drug products, taking into consideration problems inherent in the transfer of technology from research to production, from other sites, or within the site.
Conducts tests and measurements throughout stages of production to determine control over applicable variables.
Investigates deviations that occur on the manufacturing floor. Performs root-cause analysis and identifies appropriate, effective corrective actions. Implements corrective actions in conjunction with the appropriate enabling groups, i.e. engineering, maintenance, quality, validation, environmental health and safety.
Leads technical improvement projects aimed at defect reduction, improved equipment reliability, and better equipment utilization.
Serves as customer project manager on equipment purchases or improvements; interface closely with engineering to specify user requirements, review and approve drawings, define project scopes.
Collaborates with and influences other enabling departments (Quality, Engineering, Maintenance, etc.) to assure initiatives are successful.
Provides concise and thorough updates on initiatives to site leadership.
Mentor junior level colleagues inside and outside of department.
Bachelor of Science or Arts degree in a technical field such as Biomedical, Chemical, Electrical, Mechanical or Computer Engineering with minimum 10 years’ experience.
Master’s Degree in a technical field such as Biomedical, Chemical, Electrical, Mechanical or Computer Engineering with minimum 3 years’ experience.
Pharmaceutical or manufacturing experience and strong, demonstrated technical skills exhibited in a cGMP environment are requirements.
Specific knowledge of and experience with Drug Product processing and equipment in highly automated aseptic preparation, formulation, filling, isolator, or lyophilization systems is highly desirable.
Job will include standing, walking, and sitting. Occasional lifting may be required.
Aseptic gowning training may be required. Job may also require occasional weekend/evening work supporting a 24-hour/7-day operation.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Up to 25% domestic and/or international travel
Other Job Details
Last Date to Apply: September 28, 2020
Eligible for Relocation Package
Eligible for Employee Referral Bonus
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EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.