Pharmaceutical Engineer - Afton Scientific : Job Details

Pharmaceutical Engineer 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® 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. Serving clients in 18 CountriesSuccessful NDA and ANDA drug registrationsIn good standing with the FDA, PMDA, and MHRA 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 equipmentEvaluating, selecting, and ordering parts and components required for engineering batchesReviewing and modifying production instructions and operating procedures as they relate to process validationAt times, the direct supervising of production operations and occasionally, hands on work in the setup and preparation of sterile pharmaceuticals and componentsDeveloping and improving product and processesMaintaining validation operations in compliance with cGMPsInteracting with clients, suppliers, and consultants as it relates to the engineering functionWrite, review and edit master documents as applicable: SOPs, batch records, validation protocols and reports Marginal Functions: In-depth knowledge of HMI, PLC, motion controls, materials, and manufacturing processes is a plus.Work experience in FDA regulated industry is a plus. Requirements for Education and Work Experience: · Bachelor's degree in Engineering (Chemical or Mechanical preferred). · One year of manufacturing experience required. Pharmaceutical experience preferred. · Working knowledge of software tools (MS Office Suite and other software) Other Requirements: Exceptional organizational, customer service, interpersonal communication skills with the flexibility to thrive in a fast paced, changing environment and the ability to actively participate and sometimes lead cross functional teamsAbility to work independently with little to no instruction on routine workExercises judgment within generally defined practices selecting an approach for obtaining solutionsExcellent communication and interpersonal skillsAdaptable to changing priorities as project demands change.Team player contributing to a positive, collaborative working environmentExtended work hours may be required to meet business demandsMust be able to read, write, speak fluently and comprehend the English language Physical Demands: Sedentary work. Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects.Repetitive motion. Substantial movements (motions) of the wrists, hands, and/or fingers.Close visual acuity required to perform activities such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading.PandoLogic. Category: General