quality

Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across every stage of the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and...

Alternate Job Title: Senior AnalystThe Senior Product Quality Assurance (PQA) Analyst has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is responsible for supporting the day to day Quality Assurance activities related to the TPM plants including but not...

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-class manufacturing industry in Puerto Rico & USA. Responsibilities: The Contingent...

*Supplier Quality Analyst**Location:* Onsite – 100%*Schedule:* Monday–Friday, 8:00 AM–4:30 PM*Job Summary*We are seeking a detail-oriented *Supplier Quality Analyst* to support supplier quality management activities within a regulated pharmaceutical or medical device manufacturing environment.The individual will be responsible for managing...

About MGD Industrial Corp.MGD Industrial Corp. provides specialized engineering, technical staffing, quality, validation, manufacturing support, and compliance services to companies operating in highly regulated industries, including medical devices, pharmaceuticals, and biotechnology.We are actively expanding our network of qualified engineering and...

Overview As a Quality Documentation Specialist, you'll keep controlled documents and records accurate, organized, and ready for review. You'll manage document workflows, support compliance with applicable quality and regulatory standards, and partner across teams to keep production documentation clear and current. Your impact: By maintaining reliable,...

*Senior PQA Analyst – Pharmaceutical Quality Assurance**Work Arrangement:* Primarily onsite*Schedule:* Monday–Friday, 8:00 AM–5:00 PM*Job Summary*We are seeking an experienced Senior Product Quality Assurance (PQA) Analyst to support pharmaceutical Third-Party Manufacturing (TPM) operations. This position will oversee quality assurance activities at...

The Manager of Quality will be responsible for overseeing the operation of the manufacturing department and the efficacy of the overall program to make sure it has been built with compliance to legal standards and meets customer expectations. The holder of this position will also ensure continual quality improvement within the facility. The goal is to help...

Enfermera de Grado Asociado para Call Center en institución dedicada al cuidado de la salud en Carolina. Lunes a Viernes de 10am a 7:00pm y Sábados de 8:00am a 5:00pm. Libre los Domingos y un dia de la semana. Favor solicitar en: Requisitos:1.Capacidad de leer e interpretar documentos en español e inglés. 2.Dominio de MS Office y rapidez del teclado...

Viatris Pharmaceuticals LLCViatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently...

United States - RemoteJOB ID: R-****** LOCATION: United States - Remote ; Puerto Rico - Remote WORK LOCATION TYPE: Remote DATE POSTED: Oct. 27, **** CATEGORY: Quality SALARY RANGE: 132,******USD -178,****** USDJoin Amgen's Mission of Serving PatientsAt Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission—to...

Quality Assurance & Customer Support EngineerThis role has been designed as ''Onsite' with an expectation that you will primarily work from an HPE office.Who We Are:Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. We help companies connect, protect, analyze, and act on their data and applications wherever...

Title: QA Specialist III / Senior Quality AnalystLocation: Barceloneta, PR – 100% OnsiteDuration: 12+ monthsPay Range: $36/hr to $*****/hrSchedule: 1st shift – 8-5 – Monday to FridayPurposeResponsible for implementing and maintaining the effectiveness of the Quality System. Support manufacturing operations in the resolution of events, impact assessment...

For QA Services in the NPI area.WHAT MAKES YOU A FIT:The Technical Part:Bachelor's Degree with four (4) years of experience within the pharmaceutical or regulated industry.Bilingual (English & Spanish).Project Management skills.Shift: Administrative shift, and according to business needs.Experience in:NPI, Change Control, FATs, Validation, and PPQsThe...

Software Quality Engineer This role has been designed as 'Hybrid' with a requirement that you will work on average 2 days per week from an HPE office. Who We Are: Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. We help companies connect, protect, analyze, and act on their data and applications...

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and...

Entity: CSL PlasmaJob Category: QualityJob Family: Plasma CenterJob Type: Full TimeLocation: Loiza, Puerto Rico, United StatesEmployer Reference: R-******Job DescriptionResponsibilities:• Ensure center is "inspection ready" at all times by managing adherence to Standard Operating Procedures (SOPs), compliance policies and the quality system, utilizing...

Support the product complaint system at a leading biotechnology company in Juncos, Puerto Rico. You will lead and manage product complaint investigations and use data analysis and trending to detect signals early and drive timely action. What you'll do • Keep the complaints database current and accurately summarize closed investigations. • Review and...

For Quality Engieneering services in the CTW and Sustaining Projects area.WHAT MAKES YOU A FIT:The Technical Part:Bachelor's degree in Engineering, Science, or a related technical discipline, with 3–5+ years of relevant Quality Engineering experience in the medical device, pharmaceutical, or other highly regulated manufacturing industry.Bilingual, Spanish...

For Quality Engieneering services in the CTW and Sustaining Projects area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Engineering, Science, or a related technical discipline, with 3–5+ years of relevant Quality Engineering experience in the medical device, pharmaceutical, or other highly regulated manufacturing industry. Bilingual,...