Sr Engineer with experience in aseptic processing environments, including Fill/Finish operations such as vial and syringe filling lines. Experience in characterization activities and performance qualification (PQ) for New Product Introducti...
The Human Factors Lead is responsible for evaluating technician workflows, conducting cognitive load assessments, and identifying error traps in documentation and execution. This role ensures that all redesigned documents and workflows refl...
Designs, conducts and interprets biological experiments to support development programs and identifies biological pathways and agents. Provides biological scientific support to technology and product development. Reviews scientific and te...
Investigation Specialist for Solid Dosage will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. Responsibilities: Understanding of the investigat...
CSV Specialist to support the installation of several manufacturing solid dosage equipment such as but not limited to: Encapsulator Checkweigher Compression machine Hardness tester Encapsulation machine Auxiliary equipment Requisito...
Validation Specialist with hands-on experience in executing validation and qualification activities across diverse areas, including: Process Packaging Manufacturing Laboratory Computer System Validation (CSV) Software Faciliti...
The Documentation Architect designs, standardizes, and improves operational documents including batch records, SOPs, forms, checklists, and templates. This role ensures clarity, usability, and compliance using cognitive design and plain-lan...
Project Coordinator to lead the conversion of a conference room into a fully operational manufacturing line. The role involves planning activities, coordinating multidisciplinary teams, managing contractors, tracking project timelines, and ...
Document Control Associate will ensure that all manufacturing documentation for medical devices are properly created, maintained, and compliant with regulatory standards. Responsibilities: Ensure that all documents are up to date, accur...
Responsible for planning, scheduling, production activities for pharmaceutical and medical device components. Ensures efficient workflow, resource allocation, and timely delivery while coordinating with cross-functional teams and managing p...