What are the responsibilities and job description for the Pharmaceutical Engineer position at Afton Scientific. LLC?
About Afton Scientific. LLC
Providing reliable pharmaceutical services and lasting relationships within the industry for over 30 years.
Afton Scientific is a contract development and manufacturing organization (CDMO) in Virginia that specializes in small-batch filling of injectables from clinical trials to approved commercial drugs.
Utilizing 35,000 Sq. Ft of manufacturing, lab, warehouse, and administrative space, Afton provides custom, innovative solutions for clinical to commercial sterile manufacturing, packaging and labeling, analytical and micro lab services, and pharmaceutical support services.
Our Ready-To-Fill(r) line continues with our philosophy of guidance and support for our clients. It offers top-quality pre-sterilized components to those who can fill in-house.
Position Summary :
The Pharmaceutical Engineer at Afton Scientific will play a key role in validation, collaboration and execution of both new and ongoing projects and processes. This position will play a part in supporting Afton's continued growth and expansion. This role involves collaboration with leadership and various departments to ensure our success in meeting and exceeding our goals.
Essential Functions :
- Designing, executing and reporting of engineering protocols; developing process changes; and evaluating and installing new instrumentation and equipment
- Evaluating, selecting, and ordering parts and components required for engineering batches
- Reviewing and modifying production instructions and operating procedures as they relate to process validation
- At times, the direct supervising of production operations and occasionally, hands on work in the setup and preparation of sterile pharmaceuticals and components
- Developing and improving product and processes
- Maintaining validation operations in compliance with cGMPs
- Interacting with clients, suppliers, and consultants as it relates to the engineering function
- Write, review and edit master documents as applicable : SOPs, batch records, validation protocols and reports
Marginal Functions :
Requirements for Education and Work Experience :
Other Requirements :
Physical Demands :
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