- Somos un patrono con igualdad de oportunidades en el empleo que mantiene la política de emplear y retener a los mejores candidatos independientemente de la raza, color, edad, religión, sexo, origen nacional, discapacidad física o mental, orientación sexual, identidad de...
- Disponibilidad para trabajar cualquiera de los tres turnos, fines de semana, horas extras. Salario $10.50 por hora, más diferencial de turno. No requiere experiencia. Interesados favor de enviar su resume a ****** Requisitos: Disponibilidad para trabajar ...
- ...approval Lead resolution of cleaning deviations through technical knowledge, execution of supporting validation studies, and manufacturing documentation review and approval Develops and authors change controls for cleaning process or equipment changes Maintain...
- ...Responsible for the accurate and timely completion of production related cGMP documentation. Responsible for implementation of manufacturing procedures. Ensures the effective use of material, equipment, and personnel in producing quality products. Responsibilities...
- ...enhance system administration, data integrity compliance, CSV activities, and system's incidents resolution. Support of Company's manufacturing facility to ensure that cGMP's related IT Quality Systems are properly maintained in accordance to all Federal, State and...
- ...calibers, or other inspection tools - SAP experience - Familiarity with Excel - CMM operator or programming and running CMM - Manufacturing experience - Surface plate inspection Machine shop math null We are a company committed to creating diverse and...
- ...Your work will have real-world impact, and you’ll be supported in achieving your career goals! The HR Manager will support our manufacturing facility in Manati, PR. They will partner with the local HR team and site people leaders, and report functionally to Field HR...
- ...(and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?...
- ...Information Systems/Engineering or related discipline. • At least (5) years of experience validating laboratory computerized systems in a manufacturing environment, and training in validation methodologies, technologies, and process control computer systems • Knowledge on...
- ...For Validation services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Life Science or Engineering and five to seven (5-7) years of exposure in manufacturing activities within the Pharmaceutical industry. Bilingual...
- ...00 AM - 4:00 PM (pueden haber horas extras) Descripción del Puesto Nuestro cliente, líder en la industria de construcción y manufactura de asfalto en Puerto Rico, está buscando un Operador de Planta a tiempo completo. El candidato ideal será responsable de operar y...
- ...identification, pH test, osmolality, density, protein concentration, and other analysis related to the release of the products being manufactured. In addition, do microbial analyses of manufacturing utilities (i.e. water, clean condensate, compressed air, nitrogen, etc.)...
- ...(and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?...
- ...own computer systems and automation equipment are operational. The scope includes automation systems and equipment that supports manufacturing, packaging, engineering and utilities and other similar systems. The resource will be primary focus to ensure reliable and...
- ...services. This position must comply with all security Guidelines, Environmental Health and Safety regulations and the current good manufacturing practices for the job function. MAJOR DUTIES AND RESPONSIBILITIES: Schedules and completes the employee regulatory medical...
- ...eligible for shift differential Key Responsibilities Performs corrective, preventive, and predictive maintenance for Parenteral Manufacturing equipments. Supports the Parenteral Technicians in performing problem-solving and troubleshooting on the Parenteral...
- ...Candidate should be comfortable to work in any shift Purpose: Perform microbiological testing required for water used in the manufacturing process, raw materials, in process samples and final product following specifications. Perform microbiological testing such...
- ...issues or concerns promptly and effectively. 6. Quality Assurance and Compliance Ensure all project activities comply with Good Manufacturing Practices (GMP) and other relevant regulations. Implement quality control measures to ensure high standards of workmanship....
- ...validation cycles. Provide validation support for process and/or equipment upgrades, replacements, and modifications in the manufacturing and laboratory environments. Develop, organize, analyze, and present interpretations of results for operational issues or validation...
- ...on Twitter , Facebook , Instagram , YouTube and LinkedIn . Job Description Provides direct support to the manufacturing and laboratory systems and applications, including but not limited to SAP, MES, POMSnet, LIMS. Applies relevant principles to support...
- ...(and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?...
- ...challenge? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Develop and implement cleaning validation protocols for manufacturing equipment and processes. Perform risk assessments to identify critical cleaning parameters and potential residues. Design...
- ...Responsibilities Coordinates resolution of problem relating to quality and performance of purchased materials with suppliers and Manufacturing Quality Assurance. The incumbent monitors and manages implementation of new and existing processes that ultimately impact...
- ...For Process Validation services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor in Life Science or Engineering with five (5) years of exposure in Process Validation activities within the Pharmaceutical Industry. Excellent written...
- ...Work Schedule Third Shift (Nights) Environmental Conditions Office Discover Impactful Work: Review manufactured lot documentation to ensure good documentation practices (GMP) were followed and that all the required documents were present. Verify accurate...
- ...For Process Validation services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor in Life Science or Engineering with five (5) years of exposure in Process Validation activities within the Biotechnology Industry. Excellent written...
- ...situations. Physical Requirements: General office environment, ability to sit for long periods. Ability to move about in office and manufacturing facilities. Ability to travel as required, up to 10% and work non-standard business hours/flexible work style and approach based...