DESCRIPTION:
Supervise Engineers an******** for engineering design an********,an******** operational support for successful an******** Manufacturingoperations
Subject Matter Expert, acting as the focal point for processengineering ******** including troubleshoot******** plant ********investigations an******** improvements
In a cGMP env******** lea******** relate******** modificationsan******** to processes an********, troubleshoot******** deviation******** identification an******** of corrective an******** actions
Responsible for maintaining key regulatory documents an********drawings in current status an******** implementation of Goo********Practices on site
Assist in the developmen******** of Capital projects an********programs
Act as one of the key focal points for Quality topics such as ********change management, investigations an******** a Subject Matter Expert,front regulatory au******** when needed.
Actively engage in developing specifications for process equipmentan******** in Comm******** ******** FAT/SAT of relate********, as partof new build-outs
Assist in recru******** nurturing an******** of employees to supportongoing an******** business needs as well as actively seek avenues toimprove operational efficiency to accrue benefits to the business
QUALIFICATIONS:
Degree in Mechanical/Chemical Engineering or equivalent with at least10 years of relevant work experience in a pharmaceutical/biotechfacility an******** knowledge of cGMP. Hands-on experience in start-ups,commissioning an******** of process equipment
Proficiency in MS Office an******** CAD preferred
Outstanding technical knowledge in Biotech or Chemical processesan********
Excellent team player with ability to plan, organize an********projects from conception to completion as well as ability tolea********-functional teams an******** contractors
Excellent Leadership with goo******** an******** as well as verbalan******** communication skills.