Prin Employee Relations Specialist - Juncos

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 ...

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. · ...

We are seeking a talented Calibration Documentation & Planning Specialist to support calibration planning and documentation activities. · Key Responsibilities · Support calibration planning activities for a group. · Perform documentation review and management for calibrations exe ...

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 ...

We are seeking a Computer System Validation (CSV) Specialist with more than five years of experience in the biotech industry to support validation activities for regulated computerized systems. · Support planning, execution, and documentation of computer system validation activit ...

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

+Job summary · Specialist QA with experience in NPI, Change Control, Documentation Review, Validation, PPQ · ,+Qualifications · Doctorate or Masters 2 years of directly related experience or Bachelors 4 years of directly related experience or Associates 8 years of directly relate ...

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 ...

The Commissioning and Qualification (C&Q) Specialist for Process Equipment will lead and execute the commissioning and qualification activities for syringe filling lines in a regulated GMP environment. · The role requires expertise in process equipment validation, · including fil ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · Specialist Tech Engineering · The Specialist Tech Engineering will provide technical engineering support on all system/equipment optimization strate ...

Specialist QA with experience in Aseptic Process NPI Change Control FAT's Validation PPQ's. · ...

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 ...

The Commissioning and Qualification (C&Q) Specialist for Utilities and Facilities is responsible for ensuring the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · This includes HVAC systems, water systems (e.g. ...

The Commissioning and Qualification (C&Q) Specialist for Utilities and Facilities ensures the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · This includes HVAC systems, water systems (e.g., WFI, RO/DI), clean ...

We are seeking a skilled Computer System Validation (CSV) Specialist to support a fully onsite project with one of our key clients. · Develop, review, and execute validation deliverables. · Evaluate systems according to client and regulatory requirements. · ...

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 ...

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 ...