Role Summary
Process Engineer reports to the Manager of Technical Services and plans, executes and functionally directs Process/Cleaning Validation/Study assignments and projects, which require sound pharmaceutical/engineering skills and independent judgment. Works as a team member, educates internal partners on the projects, monitors and executes. Maintains effective and cooperative relationships with all departments within and outside the organization. Managing the post approval projects.
Responsibilities
- Prepare validation protocols & reports for manufacturing process and cleaning process qualification, data analysisand prepare reports; execute the manufacturing process and cleaning process qualification/validation/study.
- Managing the post approval projects. coordinating with cross functional Teams and ensuring the timely completion of projects.
- Analyzes statistical data, products or functional specifications to determine conformance with standards andestablished quality requirements
- Coordinate/oversee the development of new processes or troubleshoot existing ones
- Assist in deviation/investigations to identify root causes and define corrective and/or preventative actions (CAPA) & assist in various audits
Qualifications
Education
- Bachelors Degree (BA/BS) Pharmaceutical/Biomedical Engineering - Required
- Master Degree (MS/MA) Pharmaceutical/Biomedical Engineering - Preferred
Experience
- 2 years or more in Pharmaceutical/Manufacturing Industry
Skills
- Excellent verbal and written communication skills - Advanced
- Proficiency in MS Word/Excel/ PowerPoint/MS project - Advanced
Specialized Knowledge
- Basic Analytical Knowledge desirable. In-depth knowledge of manufacturing equipment and processes for Solid Oral, Medical Device, Transdermal, Topical and Liquid Orals.