Specialist Manufacturing - 35451 - Juncos, PR
Jornada completa
Integrated Services For Productivity & Validation, Inc
- Experience of bio-processing unit operations
- Knowledge in Root Cause Analysis methodologies
(Fishbone, Six Boxes, Fishbone, 5 Why’s, Kepner Tregoe)
- Familiar with Lean Manufacturing Practices]
- Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.
- Proficiency in GDP (Good Documentation Practices) on a regulated environment
- Knowledge in systems/Tools: Trackwise, VEEVA, MES, Smart Sheet, ChatGPT, Copilot, Power BI, Spotfire, CDOCS, and process monitoring platforms
- Strong Technical Writing/presentation abilities, and excellent written/verbal communication skills in English and Spanish
- Teamwork Oriented
- Able to work under minimal supervision and/or high workload and pressure
- Able to work extended hours
- Excellent interpersonal skills
Requirements
Doctorate OR Masters + 2 years of Manufacturing Operations experience
Alternatively, Bachelors + 4 ye
ars of Manufacturing Operations experience
Alternatively, Associates + 8 years of Manufacturing Operations experience
Alternatively, High school/GED + 10 years of Manufacturing Operations experience.
Preferred: Educational background in Life Sciences, Biology, Chemistry, and/or Engineering.Vacante publicada el 2 días atrás
Empleos similares que podrían interesarleBasado en la vacante Specialist Manufacturing - 35451 - Juncos, PR en Juncos
- ...Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes, and GMP pharmaceutical manufacturing systems. Knowledge in SAP, TrackWise, electronic batch records (PAS/X) , and documents management systems (Veeva). Requirements...SugeridoContrato
- ...Engineering Experience in Manufacturing Operations – Hands-on experience in process engineering, man ufacturing support, or production systems within a regulated environment (biotech, pharmaceutical, or similar). Technical Knowledge – Familiarity with automation...SugeridoContrato
- ...leading clients in Puerto Rico . Administrative Shift Description: With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process...SugeridoTrabajo por turnos
- ...Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes, and GMP pharmaceutical manufacturing systems. Knowledge in SAP, TrackWise, electronic batch records (PAS/X) , and documents management systems (Veeva). Requirements...SugeridoContrato
- Software Engineering or BA Data Science/Analytics Proficiency in Python, R, SQL, Power BI, Da tabricks, or similar analytics and visualization platforms . Familiarity with enterprise data platforms, data warehousing concepts, data modeling, and data integration...SugeridoContrato
- Nos encontramos en la búsqueda de un Operador de Equipo Pesado para integrarse a nuestro equipo de trabajo. La persona seleccionada será responsable de operar maquinaria pesada y apoyar las operaciones diarias en proyectos de construcción, garantizando el movimiento seguro...
- ...leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic... ...safety, purity, quality, and efficiency of the product(s) manufactured Responsible for ensuring that the Electronic Batch Record...ContratoTrabajo por turnos
- ...skills. • Ability to work in teams and adapt to continuously evolving environments. • Excellent understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). • Ability to work independently with demonstrated skills in leading...Contrato
- ...Description: With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation,... ...in BOM's (Bill of Materials) Serves as a peer-recognized specialist in at least one area, with overall responsibility for...Trabajo por turnos
- ...management skills on identifying/tracking actions and achieving due dates Requirements Doctorate OR Master’s + 2 years of Manufacturing Operations experience Alternatively, Bachelors + 4 years of Manufacturing Operations experience Alternatively, Associates...Contrato
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing to a world...ContratoTrabajo por turnos
- ...For Manufacturing Services in the Quality Systems a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with five (5) years of experience as a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project...ContratoTrabajo por turnos
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing to a world...ContratoTrabajo por turnos
- ...leading clients in Puerto Rico . Administrative Shift Description: With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process...Trabajo por turnos
- ...include but are not limited to: • Own change controls for manufacturing process changes • Support major/trend deviation... ...in BOM's (Bill of Materials) • Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining...Contrato
- ...sample management to cleaning activities associated with the manufacturing process. * Proficient with KNEAT execution * Design and... ...admin. hours, based on project needs Location: Carolina, PR / Juncos, PR Education: Bachelor's in science,Pharmacy or Engineering...De duración determinadaTiempo completoTrabajo por turnos
- Experience in parenteral products, vision system, device assembly and packaging. Requirements Doctorate OR Masters + 2 years of Engineering experience Alternatively, Bachelor’s in engineering + 4 years of Engineering experience.Contrato
- ...substances. • Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), and...Contrato
- Estamos en la búsqueda de un electricista responsable y con experiencia en proyectos de construcción para unirse a nuestro equipo. Esta posición requiere conocimientos sólidos en electricidad, compromiso con la seguridad y disponibilidad para adaptarse a los distintos ...Turno rotativo
- ...regulated environment. Protocol Development and execution requirements. • Work with other business functions such as research, manufacturing, process development, utilities, facilities, quality assurance and validation departments to support complex systems and/or...Contrato
- ...troubleshooting activities, process optimization strategies, upgrades, replacements, and modifications to the process or equipment in the manufacturing operations. Ensure that all operations are accomplished in a compliant manner consistent with current corporate policies,...ContratoTurno de nocheTrabajo por turnos
- ...company that provides services to the manufacturing industry ( Medical Devices, Pharmaceuticals... ...are seeking Validation Engineers or Specialists to support Validation/Qualification... ...note that this is an on-site position in Juncos, Puerto Rico (M–F) with availability for...ContratistaTiempo completoFin de semana
- Experience with Supplier Engagement, Cross-functional leadership and/or Project Management Requirements Doctorate degree OR Master’s degree and 2 years of Quality experience Alternatively, Bachelor’s de gree and 4 years of Quality experience Alternatively...Contrato
- ...For Manufacturing Services in the Quality Systems a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with five (5) years of experience as a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project...ContratoTrabajo por turnos
- ...For Manufacturing services in the Engineering a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering... .... Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining...ContratoTrabajo por turnos
- ...qrcgroup.com / to learn more about our services and solutions! Job Description We are seeking a QA Specialist to provide quality oversight for manufacturing operations, validation activities, facilities, and environmental programs, ensuring compliance with GMP...Contrato
- ...leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic... ...and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good...ContratoTurno de noche
- ...For maintenance services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Associate Degree with two (2) years of experience in industrial mechanics within the regulated industry. Bilingual (English & Spanish). Project Management skills...ContratoTrabajo por turnos
- ...(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?...ContratistaContratoTrabajo por turnos
- ...Republic, Mexico, Germany, Canada, and South America. Job Description At least five (5) years of directly experience in a manufacturing operation or quality role in Parenteral or Pharmaceutical Industry 2. Two (2) years of experience in GMP Cleaning activities, Clean...Tiempo completoTrabajar en la oficinaTurno rotativoTrabajo por turnosFin de semana
¿Desea recibir más vacantes?
Suscríbase y reciba vacantes similares a Specialist Manufacturing - 35451 - Juncos, PR. ¡Sea el primero en aplicar!
