Specialist Quality Complaints 35405
Jornada completa
Inteldot
Inteldot has over 15 years in the life sciences industry, with operations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Administrative Shift
Job Description:
Primary responsibilities include supporting the product complaint system at Amgen through; leading and managing product complaint investigations, performing data analysis and trending of complaint information to proactively detect signals and take appropriate actions in a timely manner.
Requirements & Qualifications:
- Strong project management skills, experience leading cross-functional teams, and the ability to handle multiple projects simultaneously is a must.
- Excellent written and verbal communication skills, including facilitation and presentation skills.
- Able to work in a team-oriented, matrix environment and work effectively with diverse departmental groups.
- Be self-motivated, able to interface effectively with various levels, attentive to details and able to prioritize and meet deadlines, and must possess excellent leadership, problem solving, analytical, influencing and customer service skills to operate and deliver results in a matrix-managed GMP environment.
- Computer literacy, independently understand, follow and implement instructions, work independently or as a team player and collaborate with outside resources, and the ability to evaluate issues, make decisions and determine when to escalate, as necessary.
- Experience in project management, Root cause analysis, CAPAs determination.
- Quality mind set and deep compliance knowledge.
- Proficient in Microsoft Office Program (Excel, outlook), usage of Team and proficient in Artificial intelligence programs (ChatGPT).
Education
- Doctorate OR Masters + 2 years of directly related experience OR Bachelors + 4 years of directly related experience OR Associates + 8 years of directly related experience OR High school/GED + 10 years of directly related experience
- Preferred: Bachelor in engineering (preference Industrial) Master in science related.
Vacante publicada el 3 días atrás
Empleos similares que podrían interesarleBasado en la vacante Specialist Quality Complaints 35405 en Juncos
- ...Experience in project management, Root cause analysis, CAPAs determination. Quality mind set and dee p compliance knowledge. Proficient in Microsoft Office Program (Excel, outlook), usage of MS Teams and proficient in Artificial intelligence programs (ChatGPT)...CalidadContratoTrabajar en la oficina
- ...more about our services and solutions! Job Description We are seeking a Specialist Quality Complaints . The primary responsibilities include: Supporting the product complaint system through: leading and managing product complaint investigations...CalidadContratoTrabajar en la oficina
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented... ...Rico & USA Responsibilities: Supporting the product complaint system; leading and managing product complaint investigations,...CalidadContratoTrabajar en la oficinaTrabajo por turnos
- ...For Quality Complaints services in the Operations & Transformation area. WHAT MAKES YOU A... ...into the database accurately. Ensure complaint-related investigations are concise,... ...and complexity of the complaint, the specialist may be responsible for conducting and...CalidadContratoTrabajar en la oficinaTrabajo por turnos
$55 por año
...you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. Quality Specialist We are seeking a Quality Specialist to join our pharmaceutical manufacturing operations team. This role focuses on...CalidadPago diarioContratistaContratoTrabajar en la oficinaTrabajo por turnos- ...For Quality services in the Manufacturing/Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering or Life Sciences and at least five (5) years of experience in Quality activities within the medical device industry. Bilingual...CalidadContratoTrabajo por turnos
- ...Experience in: Environmental Monitoring, Microbial Identification, Critical Utilities, and Cleanroom Contamination Control. Quality Standards and Regulations (Annex 1, FDA Guidance, ISO - 14644-1, and USP. Data trending, statistical anlaysis, and electronic platforms...CalidadContratoTrabajo por turnos
- ...needs. Experience in: IT systems, including integrations with manufacturing equipment Computer System Validation (CSV) Quality and Compliance The Personality Part: ~ Our Next Piece is someone who treats everyone they meet like family, especially our...CalidadContratoTrabajo por turnos
- ...For Quality services in the Engineering a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering... ...fields. Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining...CalidadTrabajo 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 in a world...CalidadTrabajo por turnos
- ...our team as we help shape a brighter way forward. Document Specialist We are seeking a detail-oriented Document Specialist to support... ...-up activities * Interface with pest control manager, quality assurance, and operations teams regarding documentation needs....CalidadPago diarioTrabajar en la oficinaTrabajo por turnosLunes a viernes
- ...For Supplier Quality services in the Manufacturing/Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Engineering and a minimum of four (4) years of relevant experience, or an advanced degree with a minimum of two (2) years of relevant...CalidadContratoRemotoTrabajo por turnos
- ...Summary The Senior Supplier Quality Engineer supports the Supplier and Distribution Quality organization by managing supplier quality activities, ensuring compliance with quality standards, and maintaining approved supplier relationships. This role is responsible...CalidadContrato
- ...With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation,... ...changes in BOM's (Bill of Materials) Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining...CalidadTrabajo por turnos
- ...in BOM's (Bill of Materials) • Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining... ...staff within manufacturing, process development, and quality. • Proficiency in GDP (Good Documentation Practices) on a...CalidadContrato
- ...Specialist QA with experience in regulated industry. Knowledge in: Environmental Monitoring, Microbial Identification (Micro... ...Familiarity with the regulatory requirements and quality standards for environmental monitoring in the pharmaceutical industry...CalidadContratoTrabajar en la oficina
- 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 in a world...CalidadContratoTrabajo por turnos
- ...controls and deviations related to plants and equipment. Support maintenance and calibration functions to improve compliance and quality. Provide expertise in troubleshooting and root cause investigations. Facilitate the transfer of technical knowledge across...CalidadTiempo completoTrabajar en la oficina
- ...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...CalidadContratoTrabajo por turnos
- ...is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, consistently delivering top-quality results. Are you ready to take on this new challenge? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Inspects...CalidadContratistaSubcontratistaContratoTrabajo por turnosLunes a viernes
- ...service pro is one your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to Be The Piece? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Validation...CalidadContrato
- ...For Quality services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and two (2) years of exposure within the Pharmaceutical & Medical Devices Industry. Bilingual: Spanish and English Soft Skills: Excellent...CalidadContratoTrabajo por turnos
- ...service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to Be The Piece? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Develops,...CalidadContratoTrabajo por turnos
- Experience in handling deviations/non-conformances investigations. Skills for technical writ ing and development of reports. Knowledge and experience with root cause analysis tools (e.g. causal factors analysis, 5 Why’s). Project management skills on identifying...Contrato
- • Execute Quality disposition (approval or rejection) of bulk drug 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...CalidadContrato
- ...established by our customers, in order to perform and provide a highly effective service. We are seeking Validation Engineers or Specialists to support Validation/Qualification activities in a Medical Devices manufacturing environment. Key Requirements: Bachelor...ContratistaTiempo completoFin de semana
- ...for one of our leading clients in Puerto Rico. Administrative Shift Job Description: Under minimal supervision, support Quality Assurance program by performing a variety of key responsibilities in manufacturing, process validation, regulatory compliance, and...CalidadTiempo completoTrabajar en la oficinaTrabajo por turnos
- Experience in the Manufacturing area, specifically writing procedures, managing documents in management system (document workflow) Requirements Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience Alternatively, Bachelor's ...ContratoTrabajo por turnos
- Deviations documentation and Change Control Management. Requirements Doctorate OR Master’s + 2 years of Manufacturing Operations experience Alternatively, Bachelors + 4 years of Manufacturing Operations experience Alternatively, Associates + 8 years of Manufacturing...ContratoTrabajo por turnos
- Support manufacturing operations and EHS team to ensure full compliance with Environmental, Health & Safety (EHS) programs. Conduct EHS training and onboarding for new hires, including regulatory compliance requirements. Enforce EHS policies, procedures, and regulatory...ContratistaContratoTrabajo por turnosFin de semana
¿Desea recibir más vacantes?
Suscríbase y reciba vacantes similares a Specialist Quality Complaints 35405. ¡Sea el primero en aplicar!
