Oversee daily staffing, scheduling, and production operations in a food manufacturing environment, ensuring compliance with safety and quality standards.
Responsibilities
Create daily staffing plans
Conduct and audit employee training
Translate weekly production schedule to floor level
Support warehouse activities and campaigns within the materials management group, ensuring compliance with FDA, EPA, OSHA, IATA and client regulations.
Responsibilities
Maintain and oversee loading docks and storage areas
Inspect and label received materials
Distribute pharmaceutical materials to destinations
Operate MMG-related equipment
Maintain chemical inventory
Requirements
Bachelor's in Chemistry
Nice to have: experience in a materials management function
Ensure manufacturing activities comply with Good Manufacturing Practice, regulatory requirements, quality standards, and approved procedures; manage deviations, corrective and preventive actions, and change controls; support audits and Health Authority inspections; partner with cross-functional teams to improve manufacturing processes and quality performance.
Compensation
Salary Range:
€29,800.00 - €55,300.00
Expected Annual Base Salary Range for role: EUR 29,800-55,300.
The salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.
In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.
Responsibilities
Ensure manufacturing activities comply with Good Manufacturing Practice, regulatory requirements, quality standards, and approved procedures.
Review and approve batch records, specifications, control methods, protocols, and Quality Management System documentation.
Manage deviations, corrective and preventive actions, and change controls, ensuring robust investigation and timely resolution.
Review investigations involving out-of-specification, out-of-trend, out-of-expectation results, and system suitability test failures.
Manage product complaints and support supplier qualification activities in line with established quality requirements.
Responsible for producing high quality dough within PJ Food Service specifications, maintaining all equipment in a highly sanitized environment and ensuring all dough is handled properly.
Responsibilities
Place dough balls into clean trays according to PJ Food Service standards.
Monitor productivity standards by analyzing metrics surrounding key performance indicators.
Recommend/implement ways to improve performance.
Ensure all dough trays are properly dated, stack and down-stack proper number of trays and maintain rotation practices at proper cooling temperature(s).
Maintain and document Good Manufacturing Practice (GMP) standards on cleanliness and sanitation to insure product is free of contamination or foreign material.
Help shape packaging processes that patients can rely on by bringing deep technical and process expertise to the secondary packaging of ophthalmic products.
Compensation
Expected Annual Base Salary Range for role: EUR 31,300-58,100.
Responsibilities
Serve as technical subject matter expert for secondary packaging processes, equipment and product formats.
Provide front-line process support, ensuring safe, compliant and reliable execution of packaging operations.
Investigate deviations, complaints and process issues, identifying root causes and implementing effective corrective and preventive actions.
Support commissioning, qualification and validation activities, ensuring technically sound documentation and accurate shop-floor execution.
Drive product transfers, format introductions and launches, translating process requirements into clear, executable packaging instructions.
Requirements
Bachelor’s degree in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy or an equivalent scientific discipline
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