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PACIV, a global leader in industrial automation solutions servicing the Life Sciences sector, is seeking a IT / CSV Specialist to provide technical support for laboratory applications, systems, infrastructure, and validation activities within a pharmaceutical manufacturing environment. Support LAC/E hardware, Citrix, Windows 10 IoT, Windows Server, and network connectivity.

PACIV Inc

IT / CSV Specialist

linkup_via_bold

HOUR

Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections. Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness.

Quality Consulting Group

JT937 - SPECIALIST MANUFACTURING

partner JazzHR

YEAR

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. Provide training to maintenance and operations staff on proper documentation procedures and the use of Maximo.

Flexible & Integrated Technical Services, LLC

Documentation Specialist - Maximo

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. Picture as well an environment of healthy competition, teamwork, being ethical and of using the scientific method in all ways possible.

Quality Specialist- 02

Monitor project progress, identify risks/issues, and implement effective resolutions to support productivity and client satisfaction. 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.

PD Project Management Specialist

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. T he Personality Part: Picture yourself in a lab… with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work.

Sr Specialist QA

Bachelor’s Degree in Chemical Engineering, Mechanical Engineering, Electrical Engineering, Industrial Engineering, Biomedical Engineering, or another related engineering/scientific discipline. You’ll support Sterile Validation and/or Non-Sterile Packaging projects , working with cross-functional teams on equipment qualification, validation, project execution, and technical documentation.

Validation Engineer/Specialist

Packaging/inspection operations, strong knowledge of GDP and electronic quality systems, and the ability to collaborate effectively with Manufacturing, Engineering, and Process Development. 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.

Specialist QA

FULL_TIME

Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley. Mentor Technical Group (MTG) is seeking an experienced BAS Validation Engineer to support qualification and validation activities for Building Automation Systems (BAS), HVAC systems, environmental monitoring systems, and GMP facility infrastructure .

Mentor Technical Group

CSV Specialist

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. Responsibilities: Perform on-the-floor Plant Quality Assurance (PQA) review and approval of cGMP manufacturing processes, procedures, testing methods, documents, and production records .

JT845 - SPECIALIST QA

Attends client's GMP Buildings Quality system forums and or Management Review meetings to present environmental and critical utilities data and recommend actions based on the data evaluation. 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.

SPECIALIST QA

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. Under minimal supervision, support Quality Assurance program by performing a variety of key responsibilities in manufacturing, process validation, regulatory compliance, and quality assurance activities .

Inteldot

Specialist QA 35845

BreezyHR

Leads or leverages cross functional teams to evaluate, develop and manage projects for new product development and ongoing lifecycle management of products, processes and therapies. Manages the development and implementation process of a company's products and services involving departmental or cross-functional teams focused on the delivery of new or existing products.

JT931 - PD PROJECT MANAGEMENT SPECIALIST

Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections. 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.

JT599 - SPECIALIST MANUFACTURING

Proven attention to detail and accuracy, with the ability to process large volumes of transactions efficiently while maintaining data integrity. We offer a competitive total rewards program including health benefits, RRSP matching, Stock option, and career development opportunities.

Harris Computer Systems

Billing Specialist

Master's + 2 years of Manufacturing Operations experience OR Bachelors + 4 years of Manufacturing Operations experience OR Associates + 8 years of Manufacturing Operations experience OR High school/GED + 10 years of Manufacturing Operations experience. Participate in regulatory inspections, New Product Introductions, and Process or Equipment Modifications: Participate in the NPI process to assess requirements for documentation, materials, training, and equipment modifications.

Process Specialist Jobs in Puerto Rico

IT / CSV Specialist PACIV Inc

JT937 - SPECIALIST MANUFACTURING Quality Consulting Group

Documentation Specialist - Maximo Flexible & Integrated Technical Services, LLC

Quality Specialist- 02 Flexible & Integrated Technical Services, LLC

PD Project Management Specialist Flexible & Integrated Technical Services, LLC

Sr Specialist QA Flexible & Integrated Technical Services, LLC

Validation Engineer/Specialist Flexible & Integrated Technical Services, LLC

Specialist QA Flexible & Integrated Technical Services, LLC

CSV Specialist Mentor Technical Group

JT845 - SPECIALIST QA Quality Consulting Group

SPECIALIST QA Quality Consulting Group

Specialist QA 35845 Inteldot

JT931 - PD PROJECT MANAGEMENT SPECIALIST Quality Consulting Group

JT599 - SPECIALIST MANUFACTURING Quality Consulting Group

Billing Specialist Harris Computer Systems

Specialist Manufacturing 35599 Inteldot

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