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- ...Qualifications: Ability to communicate effectively in English in both written and oral forms. Must be at least 18 years of age. Valid driver's license with a safe driving record. Must have a professional appearance and demeanor. Physical requirements:...SugeridoPor horaTemporalContratoTrabajar en la oficinaTrabajo por turnos
$17 - $20 por hora
...inventory control. We will consider employment of qualified applicants with arrest and conviction records. Obtains and maintains valid PTCB certification or pharmacy license as required by state. An Equal Opportunity Employer, including disability/veterans. The...SugeridoTrabajo de temporadaTrabajo por turnos- ...For Validation services in the Manufacturing & Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor Degree in Engineering or sciences and at least five (5) years of experience in Validation activities within the Pharmaceutical and/or Medical...SugeridoContratistaContratoTrabajo por turnos
- ...For Validation support services in the Quality area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science with four (4) years of experience and exposure within the Pharmaceutical or Medical Devices industry . Bilingual (Spanish and English...SugeridoContratoTrabajo por turnos
- ...For Validation services in the Global Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Life Sciences or Engineering (preferrable)and at least eight (8+) years of experience in the execution of facility/utility protocol within...SugeridoContratoTrabajo por turnos
- ...according to business needs. Experience in: Ethylene oxide, steam, liquid chemical, and radiation sterilization methods Process Validation, Equipment IQ, and Computer software validation knowledge No sterile package design or pharma design The Personality Part...SugeridoContratoTrabajo por turnos
- ...enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating...SugeridoTemporalTrabajo por turnos
- ...and you might just be what we’re looking for! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Conducts a compliant validation process for quality information technology systems, which requires formal validation documentation. Coordinates activities...SugeridoContratoTrabajar en la oficinaTrabajo por turnosFin de semana
- ...contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Conduct comprehensive packaging validation and testing activities in support of Product Transfer and New Product Introduction initiatives. Interaction with packaging...SugeridoTemporalTrabajo por turnos
- ...The Packaging Engineer will be responsible for designing, developing, validating, and optimizing packaging systems to support Product Transfer and New Product Introduction (NPI) initiatives. This role requires hands-on experience working with packaging lines, filling...SugeridoContrato
- ...The Quality Application Specialist supports product transfer activities with a primary focus on process validation, sterilization processes, and commercial release readiness. This role ensures compliant execution of validation activities and quality system requirements...SugeridoContrato
- ...manufacturing sites. The most widely used are Equipment Controller (EC) and External Functions (EF). Both of these components are validated using the Global IT MSCM Procedure. All documentation from MSCM is leveraged into CSV. However, CSV has one extra step that is...SugeridoTemporalTrabajo por turnos
- ...enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: In charge of Process Validation, Equipment IQ and Computer software validation. Designs manufacturing processes, procedures and production layouts for...SugeridoTemporalTrabajo por turnos
- ...For Validation services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and (3) three years of experience within the Medical Devices Industry. Bilingual: Spanish and English Soft Skills: Excellent Technical...SugeridoContratoTrabajo por turnos
- ...For packaging validation and testing activities in Product Transfer and New Product Introduction. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and a minimum of five (5) years of experience in the regulated industry. Excellent...SugeridoContratoTrabajo por turnos
- ...Summary The Quality Applications Specialist supports quality systems and product transfer activities by ensuring compliant validation of computerized systems and manufacturing processes. The role focuses on sterilization equipment, process validation, and quality...Contrato
- ...2 years of relevant experience in a regulated industry (medical device, pharmaceutical, or similar). Experience with process validation, equipment validation, and computer software validation (CSV). Bachelor’s degree in Engineering completed Ability to manage...Contrato
- ...introduction of new products and manufacturing processes within a regulated medical device environment. The role focuses on equipment validation, process development, and ensuring manufacturing processes comply with regulatory and quality requirements. The engineer will...Contrato
- ...Quality role to support product transfer activities. focused on process validation. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering with at least three (3) years of experience within the regulated industry. Bilingual (English &...ContratoTrabajo por turnos