Job Summary: The Process Engineer reports to the Manufacturing Unit Technical Leader and is responsible for driving engineering process improvements, capital equipment upgrades, efficiency gains, and cost reduction initiatives. The role...
Job Summary : We are seeking an experienced MES Engineer with strong Pharma domain experience to support and enhance Rockwell Automation Pharma Suite (Factory Talk Production Centre) in a regulated manufacturing environment. The ideal cand...
Responsibilities: Value Stream Assessment & Process Design: End-to-end value stream definition, assessment and mapping. Value stream diagnostic including process improvement opportunities, pain-point identification, process waste etc. E...
This is a temporary 6-month contracted 1099 position with no benefits. The pay range for this position is $40-$45/hr (depending on experience) Interprets customer specifications to define requirements for mechanical designs. Performs fi...
This is a temporary 6-month contracted 1099 position with no benefits. The pay range for this position is $70-$85/hr (depending on prior experience) Job Functions: Applies expertise as an emerging authority in the mechanical engineeri...
Job Description: The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams, this individu...
Responsibilities: Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out. Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CR...
EVP, Market Access & Payer Marketing Meet is currently partnering with a leading healthcare communications agency that is looking to appoint a visionary, commercially minded Executive Vice President to lead and scale their Market Access & P...
Roles & Responsibilities : Monitor due dates for lab instrument reviews and coordinate with stakeholders. Execute SOP-driven validations, produce IQ/OQ/PQ deliverables, and ensure ALCOA+data integrity. Perform gap analyses, remedi...
Responsibilities: This role is responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process and sustaining engineering projects, ensuring compliance with FDA and EU regulation...