Empleos: associate specialist

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...

At Kelly Science, Engineering, Technology & Telecom (SETT), we're passionate about helping you find a job that works for you. How about this one? We're seeking for a Specialist QA to work in the east region, in PR. With us, it's all about finding the job that's just right.This job might be an outstanding fit if you have:Doctorate OR Master degree in Life...

Company DescriptionQRC 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 to learn more about our services and solutionsJob DescriptionSpecialist QA with experience in:Aseptic ProcessNPIChange ControlFAT'sValidationPPQ's...

Specialist QA with experience in NPI, Change Control, Documentation Review, Validation, PPQ, FAT. RequirementsDoctorate or Masters 2 years of directly related experience or Bachelors 4 years of directly related experience or Associates 8 years of directly related experience Bilingual (Spanish/English)(Write/Speak)

Specialist QA with experience in: Aseptic Process NPI Change Control FAT's Validation PPQ's​ RequirementsDoctorate or Master's 2 years of directly related experience or Bachelor's 4 years of directly related experience or Associate 8 years of directly related experience Bilingual (Spanish/English)(Write/Speak) ...

For Packaging services in the Engineering areaWHAT MAKES YOU A FIT: The Technical Part:Bachelor's Degree in Engineering with five (5) years of Engineering experience within the pharmaceutical or medical device industry.Bilingual (English & Spanish).Project Management skills.Shift: 1st and 2nd (8hrs), and according to business needs.Experience...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.We are seeking a talented, dedicated...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...

The Associate Quality Application Specialist supports the validation, administration, and compliance of quality-related computerized systems in a regulated environment. This role assists with validation documentation, system configuration, and cross-functional coordination to ensure compliance with applicable federal and international regulations. ...

For Quality services in the Quality area.WHAT MAKES YOU A FIT: The Technical Part:Bachelor's Degree in Life Sciences or Engineering and previous exposure within the Pharmaceutical & Medical Devices Industry.Bilingual: Spanish and EnglishSoft Skills: Excellent Communication skillsShift: 1st Shift. Experience in:Six Sigma, CAPA, and Product...

At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what you need to make it happen. It won't always be easy, growing takes grit. But at ABB, you'll never run alone. Run what runs the world.This Position reports to:Production Development...

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices...

Company DescriptionQRC 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 to learn more about our services and solutionsJob DescriptionSpecialist QA with experience in NPI, Change Control, FAT, Validation and...

The Quality Assurance Specialist provides quality oversight and support for regulated manufacturing operations, ensuring compliance with current Good Manufacturing Practices (cGMP), regulatory requirements, and internal quality systems. This role performs QA review, approval, and leadership activities under minimal supervision and serves as a key quality...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.We are seeking a talented, dedicated...

CompanyBrief DescriptionGlobal Rescue is the world's leading membership organization providing integrated travel risk management services, including medical, security, intelligence and crisis response services to consumers, enterprises and governments. Founded in 2004 Global Rescue's unique operational model provides best-in-class services that identify,...

POSITION SUMMARYThe Clinical Specialist I – Pharmacy Coverage Determinations supports the Clinical Supervisor by reviewing and making decisions on pharmacy benefit coverage requests, including formulary exceptions, prior authorizations, step therapy, and quantity limit exceptions. The role involves evaluating clinical appropriateness, identifying...

We are an Equal Employment Opportunity Employer and take Affirmative Action to recruit Protected Veterans and Individuals with Disabilities. SUMMARY Attends all call types - from order status, billing balances and/or repair status. To create and maintain service documentations for a new service request, claim or technical situations using the systems...

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:Independently...

For Validation services in the Engineering area.WHAT MAKES YOU A FIT: The Technical Part:Bachelor's Degree with four (4) years of experience as an Engineer within the pharmaceutical or regulated industry.Bilingual (English & Spanish).Project Management skills.Shift: Administrative, and according to business needs.Be available to support non-standard...