QRC Group, LLC Jobs in United States

This role involves working with pneumatics, automatic control and vision inspection systems. The ideal candidate will have experience in maintenance activities. · ...

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

This role supports temperature and humidity mapping activities in a GMP-regulated pharmaceutical environment. · Analyze temperature data from thermal studies. · Prepare technical reports including data analysis, graphs, conclusions. · ...

This is a validation specialist position with hands-on experience in executing validation and qualification activities across diverse areas. · ', ...

We are looking for a creative,motivated,and strategic Recruiter & Social Media Specialist to strengthen our digital presence,increase traffic to our job postings,and attract highly skilled professionals to join our talent community. · The Recruiter & Social Media Specialist is re ...

Sr Engineer with experience in regulated environments and ability to apply GMP in manufacturing and validation. · Doctorate or Masters + 2 years of Engineering experience or Bachelor's in engineering + 4 years of Engineering experience. · Bilingual (Spanish/English)(Write/Speak) ...

+Summary: · Responsible for configuration and simulation on Checklist Manager application (prototypes and reports). Must have knowledge of databases and the SQL language (for reports that's critical) and experience in the pharmaceutical industry. · +Assist the document owner to d ...

Designs, conducts and interprets biological experiments to support development programs and identifies biological pathways and agents. · Provides biological scientific support to technology and product development. · Reviews scientific and technical summaries, and provides recom ...

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

This role contributes to enhancing product quality operational efficiency and safety while assisting in engineering projects equipment upgrades facility modifications. · Responsibilities · Support automation systems troubleshooting Assembly machinesfixtures label applicator robot ...

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 ...

Support the installation of manufacturing solid dosage equipment such as encapsulator checkweigher compression machine hardness tester and more Main activities include verification of equipment installed and configured at vendor site FAT implement progression from FAT through IOQ ...

Process validation specialist with experience in ethylene oxide sterilization processes to guarantee effectiveness and safety for medical or industrial products. · Develop IQ/OQ/PQ validation protocols for EtO sterilization processes. · Conduct load configuration studies, gas pen ...

Data entry clerk responsible for accurately inputting data and updating existing records in digital databases. · This role ensures that information is maintained with precision and supports the smooth operation of business processes. · ...

The Licensed Pharmacist is responsible for ensuring compliance with all applicable pharmaceutical regulations, Good Manufacturing Practices (GMP), and company policies. · Responsibilities: · Act as the Pharmacist-in-Charge for the site, maintaining an active professional license ...

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. · ...

The Process Development Scientist will have expertise in Automated Visual Inspection (AVI), including machine vision–based inspection platforms. · ...

Sr Engineer with knowledge and experience with:cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, and equipment. · Change control, non-conformace, corrective and preventive actions, and validation practices.    · Maximo. · Worki ...

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

Sr Associate Tech Engineering with knowledge on: Mechanical equipment adjustment/troubleshooting. · PLC Systems troubleshooting-Rockwell · Vision Systems troubleshooting/adjustment-Cognex · cGMP's  · Systech vision systems · FDA regulation  · Basic control systems hardware · Req ...