A Facility and Maintenance Technician is responsible for keeping the facility and production equipment operating, repairing any problems when they are discovered before they have a chance to worsen. This role performs regular preventive/reactive maintenance on equipment and the facility.
Responsibilities
installing/troubleshooting/repairing production equipment and maintenance on the facility
Performing routine maintenance around the building such as fixing structural damage, repairing windows, door or wall repair, and changing light bulbs
Performing troubleshooting and repair of production related equipment (Arburgs, Makino, EDMs, Grinders, Chillers)
Completes routine maintenance of all equipment used in the facility (production equipment, compressors, chillers, water tower)
Repairing broken or leaking plumbing to avoid water damage and restore full use of water fixtures, address leaks, clogs or other drainage problems
A Facility and Maintenance Technician is responsible for keeping the facility and production equipment operating, repairing any problems when they are discovered before they have a chance to worsen. This role performs regular preventive/reactive maintenance on equipment and the facility.
Responsibilities
installing/troubleshooting/repairing production equipment and maintenance on the facility
performing routine maintenance around the building such as fixing structural damage, repairing windows, door or wall repair, and changing light bulbs
performing troubleshooting and repair of production related equipment (Arburgs, Makino, EDMs, Grinders, Chillers)
completes routine maintenance of all equipment used in the facility (production equipment, compressors, chillers, water tower)
repairing broken or leaking plumbing to avoid water damage and restore full use of water fixtures, address leaks, clogs or other drainage problems
Provide end-to-end regulatory support for pharmaceutical development and commercialization programs, including IND/NDA submission management, health authority interactions, and lifecycle maintenance.
Responsibilities
Lead or support IND and NDA submission management
Coordinate health authority meeting requests and correspondence
Prepare and coordinate lifecycle submissions
Conduct regulatory intelligence searches
Prepare global regulatory team materials
Requirements
Bachelor’s degree in a scientific, technical, or related discipline
Regulatory Specialist I responsible for processing licensing applications, interpreting statutes, and maintaining records in the Florida Department of Agriculture and Consumer Services.
Compensation
Salary: $41,000.18 - $44,169.58
Responsibilities
Responds to telephone, email, paper correspondence, and faxed inquiries regarding statutory and procedural eligibility requirements for initial applications and renewal applications
Interprets policies, procedures, applicable Florida Statutes, and reciprocity
Reviews applications, investigative reports, verification reports, fingerprint analyses, and other associated documents to determine the action(s) required to complete the processing of an application or renewal application
Assists applicants, licensees, agency owners, law enforcement personnel and division personnel with licensing requirements or procedures
Advises applicants of any action required to continue the application or renewal process
Responsable de Projet Affaires Réglementaires Globales intervenant sur un périmètre international, principalement centré sur les procédures européennes.
Locations (2)
Agen, Lot-et-Garonne, France
Rueil-Malmaison, Île-de-France, France
Responsibilities
Apporter son expertise réglementaire afin d’obtenir les enregistrements en Europe
Mettre en œuvre les décisions de stratégie réglementaire définies par le Global Regulatory Plan
Rédiger le Module 1 européen et coordonner la constitution du dossier complet
Piloter en autonomie des procédures européennes simples
Coordonner en autonomie les activités de gestion du cycle de vie
Requirements
Bachelor’s degree in science (chemistry, biology, life-science)
The Document Control Supervisor is responsible for overseeing the daily operations of the Document Control department to ensure the accuracy, integrity, and compliance of controlled documentation within the organization's Quality Management System (QMS).
Responsibilities
Supervise the daily activities of the Document Control team, ensuring work is completed accurately and within established timelines.
Assign, prioritize, and monitor workloads to meet departmental and business objectives.
Manage the document lifecycle, including document creation, review, approval, revision, distribution, archival, and retirement.
Ensure all controlled documents are maintained in accordance with company procedures and regulatory requirements.
Administer and maintain the Electronic Document Management System (EDMS), ensuring document integrity, version control, and audit trail accuracy.
Requirements
Bachelor's degree in Business Administration, Life Sciences, Engineering, Quality, or related field
Lead quality management and safety initiatives within the Early Phase GMP Analytical Development department, ensuring compliance with regulatory standards and internal SOPs.
Responsibilities
Investigate laboratory incidents, deviations, OOS, OOT, and related quality events
Ensure all investigations are completed accurately and within timelines
Identify root causes of analytical failures and implement effective CAPA
Support audit compliance activities and ensure timely closure of audit observations
Respond to regulatory inspection observations and surveillance findings
REGULATORY SPECIALIST IState of Florida · Tallahassee, US
Responsable de projets Affaires Règlementaires Global (H/F)UPSA · Agen, France+1 more
ManagerSyngene International Limited · Bangalore, India