Process Validation Specialist - Juncos

We Are Seeking For Talented Dedicated Individuals Who Is Committed To Work Under The Highest Standards Of Ethics To And With Expertise In The Following Areas: · Packaging Validation · ...

Mentor Technical Group provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. · ...

For Validation services in the Sterile and Filling area. · Develop,, · ...

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, ...

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 ...

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. ...

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, Valid ...

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

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 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. · ...

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 ...

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 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 ...

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. · ...

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. · ...

+Job description missing · +Aseptic Process · ...

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

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. · ...

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, Valid ...