Quality Control Specialist - Juncos

We are seeking a Quality Specialist to join our team at Cencora. As a key member of our organization, you will be responsible for providing technical guidance and ensuring compliance with GMPs/CFRs. · ...

Mentor Technical Group provides technical support and solutions for the FDA-regulated industry. · Scientific Data Analysis · Technical Writing (English and Spanish) · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Specialist Quality Control. · Under general direction, functions as the technical specialist for testing and development in areas of molecular biology ...

Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · The TOP Documentation Specialist is responsible for the collection, review, organization, and delivery of Turnover Packages (TOPs) for all packaging ...

We're seeking a Specialist QA to work for one of our top Biotechnology Industry clients at Juncos, PR. · Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

The Specialist QA supports and ensures compliance with quality systems and regulatory requirements in a regulated manufacturing environment.This role is responsible for reviewing and approving quality and manufacturing documentation, · supporting investigations, managing quality ...

We are seeking a talented individual committed to work under the highest ethics standards for the following position: Quality Assurance Specialist.The QA Specialist plays a critical role in ensuring that all biotechnology and pharmaceutical products meet regulatory standards and ...

Specialist QA with experience in NPI, Change Control, FAT, Validation and PPQs. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: CQV Specialist - Smoke Testing / Airflow Visualization. · Plan and execute smoke studies (airflow visualization) for cleanrooms, RABS, isolators, filli ...

CQV Specialist for Upstream Process Equipment. · The CQV Specialist for Upstream Process Equipment will be responsible for the commissioning and qualification of systems supporting cell culture operations in a cGMP biotechnology manufacturing environment. · Bachelor's degree in e ...

This role involves working with a highly enthusiastic team in a world-class manufacturing industry in Puerto Rico & USA. · Responsibilities: · Execute equipment & test method validations · , reviews the work of other specialists; may manage some elements of projects. · ...

The Commissioning and Qualification (C&Q) Specialist for Laboratory Systems in QC is responsible for ensuring the successful implementation, validation, and qualification of laboratory systems used in Quality Control environments. · ...

We are seeking a talented, · d · dicated individual committed to work under the highest ethics standards for the following position: · QA SpecialistThe QA Specialist ensures compliance with quality systems,overses batch record reviews,and supports the implementation of new produc ...

A leader in the pharmaceutical, biotech, medical devices, and manufacturing industry is looking for a talented Manufacturing Engineer to join our team. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Validation Specialist. · ...

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. · ...

We are seeking a talented individual committed to working under high ethics standards for the position of CQV Specialist. · The ideal candidate will have prior experience with biotech processes, familiarity with regulatory standards (FDA/EU Annex 15), and ability to work cross-fu ...

We are seeking a skilled Computer System Validation (CSV) Specialist to support a fully onsite project.The ideal candidate will have strong experience in validating GxP-regulated systems. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Specialist QA. · ...