How will you make an impact?

• Technically supports day-to-dayManufacturing Sciences and Technologyin the Manufacturing, Filling, Freeze Drying, and/or Packaging areas of theSterilesbusiness unit.

• Investigates, creates, and validates scientific methodologies used to control raw materials, production intermediates, and final products on a complex scope of processes, products, and projects.

• May be involved in pre-clinical, clinical, and/or post-marketing stages of drug development.

• Works on technical/scientificprocess/product/projectactivities to execute strategies and technical solutions that meet client needs and expectations.

• Evaluates and contributes to the design of manufacturing processes and supports problem solving as necessary with independent judgment.

• Makesdecisions that require developing new options to solve complex problems.

What will you do?

• Author and improve procedures including SOPs,BatchRecords,Protocols, training documents, etc. Author ChangeControls, etc.in electronic Quality Management Systemand Document Management System.

• Leads cross functional investigation teamsinCAPAclosure

• Present recommendations internally.

• Leadsassignments, including managing project timelines and deliverables.

• Liaises with internal Quality, Operations, Engineering, Validation, and other functional areas tomeet teamobjectives.

• Guides and advisesdocumentation and training strategiesduring implementation of new methodologies and processes.

• Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices and Safety guidelines.

• Maintains the necessary compliance status required by company and facility standards.

How will you get here?

Qualifications

• Bachelor of Science in any Science or STEM degree preferred. Other Education and time in industry can be considered.

• 2-4years of scientific experience (preferred), preferably in the pharmaceutical industry. Education,time inthe industry, and other applicable experiencecan be considered.

• Experience with technical writing is a plus

• Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities

• Thorough knowledge of Good Manufacturing Practices.

• Strong proficiency in Microsoft Office Suite (including Word, Excel, and PowerPoint).

• Excellent critical and logical thinking skills.

• Effective written, interpersonal, and presentation skills, including managing technical discussions with internal and external clients.

• Ability to work on multiple projects simultaneously.

• Ability to develop knowledge and skills in pharmaceutical processes, equipment, instrumentation, and procedures.

• Ability to keep current with scientific literature and industry trends relating to process technologies.

• Ability to develop technical solutions.

• Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand and walk; ability to lift and/or carry light objects of up to 25 lbs. for brief periods.