Laboratory Validation Specialist - Juncos, Juncos, Puerto Rico

· For Packaging services in the Engineering area · WHAT 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 Manag ...

The Cleaning Validation Specialist to lead and execute risk-based cleaning validation and verification activities across manufacturing operations (upstream, downstream, and fill/finish or packaging support as applicable). This role ensures compliant science-driven strategies for ...

The Cleaning Validation Specialist leads and executes risk-based cleaning validation and verification activities across manufacturing operations, ensuring compliant strategies for equipment cleaning, residue removal, and lifecycle management aligned with current GMP and global he ...

· For Validation services in the Sterile and Filling area.   · WHAT MAKES YOU A FIT:  · The Technical Part: · Bachelor's Degree in Life Science or Engineering and a minimum of five (5) years of experience in the regulated industry.   · Excellent written and verbal skills in both ...

· Company Description · Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Manag ...

Quality Consulting Group is looking for a talented and motivated validation specialist to join their team. The role involves working with a highly enthusiastic team in the pharmaceutical industry in Puerto Rico & USA. · ...

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. · The ideal candidate has hands on experience using Kneat and is well versed in CSV requ ...

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

Specialist QA with experience in NPI and Change Control.Requirements include a Doctorate or Masters degree + 2 years of related experience or Bachelors + 4 years of related experience. · ...

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

We are seeking an experienced Specialist QA with expertise in NPI, Change Control, Documentation Review, Validation, PPQ, · FAT. · Doctorate or Masters + 2 years of directly related experience or · Bachelors + 4 years of directly related experience or · Associates + 8 years of di ...

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

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

This job involves working as a Specialist QA with experience in Aseptic Process NPI Change Control FAT's Validation PPQ's. · Bachelor’s + 4 years of directly related experience or Associate + 8 years of directly related experience Bilingual (Spanish/English) · ...

Specialist QA with experience in Quality and Compliance. · ...

We are looking for a talented and highly motivated manufacturing engineer to join our team in Puerto Rico & USA. · ...

Lead and support manufacturing projects for process/equipment optimization and sustainability initiatives. · ...

· Assesses impact of IT reports/applications/software/hardware changes on process and equipment · Coaches and reviews work of lower-level specialists · ...

We are looking for a manufacturing engineer to join our team. The ideal candidate will have a bachelor's degree in engineering and four years of experience in the medical devices industry. · The successful candidate will be responsible for executing equipment and test method vali ...

· ...