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9 Hours Ago
Greendale, IN, USA
13,715 Employees
Entry level
13,715 Employees
Entry level
Biotech • Pharmaceutical
As a Quality Specialist I, you will perform quality audits on production and packaging processes, ensuring compliance with quality standards. You'll document non-compliance, report issues, and support the Quality Assurance team. The role involves using a computer for data tracking and requires knowledge of GMP and food safety regulations.
9 Hours Ago
Madison, WI, USA
13,715 Employees
Entry level
13,715 Employees
Entry level
Biotech • Pharmaceutical
The Process Engineer will support manufacturing processes by enabling technology transfer, authoring batch documentation, and collaborating cross-functionally to enhance efficiency. Responsibilities include evaluating existing processes, identifying improvements, and supporting operational success through documentation and technical oversight in a GMP environment.
9 Hours Ago
Philadelphia, PA, USA
13,715 Employees
Mid level
13,715 Employees
Mid level
Biotech • Pharmaceutical
The Continuous Improvement Specialist at Catalent enhances operational efficiency by implementing Lean practices and supporting CI efforts. Responsibilities include leading projects using Lean Six Sigma tools, coaching project leaders, and fostering a Continuous Improvement culture across teams.
9 Hours Ago
Madison, WI, USA
13,715 Employees
Entry level
13,715 Employees
Entry level
Biotech • Pharmaceutical
The Engineer – Automation is responsible for managing and optimizing production and laboratory automation systems, including PLC and database management. The role involves supporting equipment qualification, leading improvement projects, and ensuring compliance through documentation and training. This position emphasizes collaboration with various engineering disciplines to enhance operational technology initiatives.
9 Hours Ago
Philadelphia, PA, USA
13,715 Employees
Senior level
13,715 Employees
Senior level
Biotech • Pharmaceutical
The Senior Engineer, Quality Operations at Catalent provides QA guidance for manufacturing and packaging, ensuring compliance with FDA regulations and handling quality complaints, process deviations, and validations. They oversee projects and compliance issues to improve quality metrics and systems.
9 Hours Ago
Greendale, IN, USA
13,715 Employees
Entry level
13,715 Employees
Entry level
Biotech • Pharmaceutical
The Assistant Quality Supervisor will lead Dietary Supplement and food manufacturing QA activities in line with Food Safety regulations and Quality programs. Responsibilities include auditing, overseeing manufacturing processes, conducting investigations, and providing training to quality assurance specialists.
9 Hours Ago
Somerset, KY, USA
13,715 Employees
Senior level
13,715 Employees
Senior level
Biotech • Pharmaceutical
The Supplier Quality Regional Lead will oversee the Supplier Auditor Team, manage audits, generate reports, and ensure compliance with quality standards. This role involves scheduling audits, developing performance metrics, and collaborating with cross-functional teams. Additionally, the lead will handle supplier notifications and support quality compliance initiatives.
9 Hours Ago
Madison, WI, USA
13,715 Employees
Mid level
13,715 Employees
Mid level
Biotech • Pharmaceutical
The Process Engineer will support technology transfer into manufacturing, collaborate with cross-functional teams, author batch documentation, evaluate processes for improvements, and ensure compliance with GMP manufacturing standards.
Yesterday
Bloomington, MN, USA
13,715 Employees
Mid level
13,715 Employees
Mid level
Biotech • Pharmaceutical
The Procurement Specialist will support local and global procurement teams in executing projects focused on cost savings and supplier performance. Responsibilities include collaborating with stakeholders, conducting supplier onboarding, managing contracts, and ensuring alignment with procurement processes to deliver business objectives.
Yesterday
Kansas City, MO, USA
13,715 Employees
Mid level
13,715 Employees
Mid level
Biotech • Pharmaceutical
The Group Lead, Quality Assurance Documentation Systems is responsible for leading the Document Control, Records Center, and Systems Administration departments. They facilitate the implementation and maintenance of documentation systems, manage departmental processes, act as a subject matter expert for SOPs, and support regulatory inspections and quality metrics. Leadership experience and a strong background in Quality Assurance are emphasized.
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