Quality Systems Validation Specialist - Juncos - Quality Consulting Group, LLC

We are looking for a Validation Specialist to join our team in Juncos, PR. As a key member of our engineering group, you will be responsible for ensuring the quality and integrity of our products. · ...

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 ...

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. · ...

For validation services in the sterile and filling area. · 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 English and Spanish. · ...

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. · ...

Specialist QA acts as technical specialist to review and approve product MP's · ...

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 ...

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+We are looking for a talented and motivated Senior Engineer to join our team. In this role, you will work with a highly enthusiastic team in the manufacturing industry in Puerto Rico & USA. · +Provides characterization of process optimization strategies and/or troubleshooting of ...