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- ...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
- ...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 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
- ...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
- ...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
- ...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
- ...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
- ...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
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...SugeridoContrato
- ...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...SugeridoContrato
- ...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...SugeridoContrato
- ...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...SugeridoContrato
- ...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
- ...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...ContratoTrabajo por turnos
- ...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:...Por horaTemporalContratoTrabajar en la oficinaTrabajo por turnos
- ...permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. ~ Ability to define problems, collect data,...TemporalInicio inmediato
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...ContratoTrabajar en la oficina
$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...Trabajo de temporadaTrabajo por turnos- ...EHSS regulations Willing to travel outside of Puerto Rico Project Management knowledge Knowledgeable on process/equipment validation Lean six sigma tools knowledge and expertise Geen Belt, Black Belt Desired Full Bilingual - written and spoken English...Temporal
- ...Select sound techniques to solve problems and make design recommendations under direction of manager. Assess results for application, validity and conformance to specifications. Prepares and controls the capital working budget for Manufacturing Projects. Utilize...Temporal
- ...process as change control owner and/or action owner on local or divisional projects. Perform and maintain process or product validations, re-validation and Validation Maintenance programs using Local or Divisional engineering resources. Generate validation protocols...ContratistaTemporalOffshore
- ...to support Manufacturing areas, New Product, Design, Introduction, Development, Transfer, Implementation, as well as Changes and Validations to existing or new products manufactured within Aibonito facilities. ~Lead and participate in multifunctional projects (ex. R&D...Temporal