qrcgroup

We are seeking a PMO-driven Project Lead to manage a flexibility program end-to-end, ensuring governance, coordination, visibility, and delivery acros...

Role Overview We are seeking an experienced, hands-on Project Manager to lead capital projects (CAPEX) in a pharmaceutical manufacturing site.The cand...

Jr Validation Specialist with experience in regulated industries to collaborate with cross-functional teams to draft project schedules and plans. Know...

We are seeking an experienced and highly organized Senior Project Manager to lead and manage a diverse portfolio of projects. This role requires a pro...

Sr. Validation Specialist support of manufacturing process and equipment upgrades, replacements, and modifications in the manufacturing, or manufactur...

Sr Engineer with knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, a...

Engineer with experience in regulated industry or knowledge in Fermentation, Cell Culture or Harvest process. Experience supporting commercial campaig...

The Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated ...

Sr Associate Manufacturing Systems with experience in FDA regulated Industries and PLC programming and troubleshooting - Rockwell. Knowledge on Vision...

Support the Engineering and Capital Projects team by coordinating project activities, managing procurement tracking, and maintaining project schedules...

The Validation Specialist is responsible for supporting qualification and validation activities for manufacturing equipment and processes. The role fo...

The Project Leader is responsible for evaluating technician workflows, conducting cognitive load assessments, and identifying error traps in documenta...

Validation Specialist with hands-on experience in executing validation and qualification activities across diverse areas, including: Process Packaging...

CSV Specialist to support the installation of several manufacturing solid dosage equipment such as but not limited to: Encapsulator Checkweigher Compr...

The Documentation Specialist designs, standardizes, and improves operational documents including batch records, SOPs, forms, checklists, and templates...

The CI/Process Analyst supports discovery, analysis, redesign, and measurement activities across the engagement. This role ensures improvements are ev...

The Training & Change Manager develops and delivers training programs that build internal capability in cognitive design, documentation practices, and...

The QA Liaison ensures the project’s deliverables meet all GMP/GxP, data integrity, and document control requirements. This role acts as a bridge betw...

We are seeking an experienced Engineer to support the design, development, and integration of automated assembly and packaging equipment in a regulate...

Associate Tech Engineering with experience with pneumatics, automatic control and vision inspection systems required. Duties: Identify, and resolve, a...