Quality Engineer III
Waco Metro Area, TX
The individual will be responsible for the review of site project documents to ensure design and execution to regulated, corporate, and site standards.
Essential Functions and Responsibilities:
The individual responsible for the work will be capable of the following:
Lead and facilitate information gathering Quality compliance discussions for equipment and processes Utilizing Microsoft Word and Adobe Acrobat for the drafting and review of product documents. Redline site policies and procedures for compliance and efficiency improvements. Provide guidance on identified redundancies.
Specifically, the successful candidate will: Support process related commissioning and qualification activities. Provide cross-functional support to other departments, as necessary; Identify quality / compliance related issues.
Direct and Indirect. Knowledge, Skills, Qualifications and Physical Requirements.
Specialized Knowledge and Skills:
Expertise in troubleshooting or developing various unit operations and/or analytical methods is beneficial. The ideal candidate will be well situated to knowledgeably discuss unit operations and analytical methods, be capable of performing complex statistical analyses using MS Excel Equipment and Applications. Work Environment and Physical Demands: Sitting, light lifting, standing, and operating a PC.
The position requires a Bachelor s Degree in Engineering or Sciences with a minimum of 7-10 years experience in Process Development, Process Improvement, or Manufacturing within the pharmaceutical industry.