QRC Group

QRC Group is seeking a dynamic and results-driven Recruiter to join our Talent Acquisition team. This role is responsible for identifying attracting and engaging top talent to support our clients workforce needs across regulated and technical industries. The Recruiter will manage the

QRC Group is seeking a dynamic and results-driven Recruiter to join our Talent Acquisition team. This role is responsible for identifying attracting and engaging top talent to support our clients workforce needs across regulated and technical industries. The Recruiter will manage the

The Methods Transfer & Validation Specialist Microbiology is responsible for planning executing and documenting microbiological method transfers validations verifications and continuous improvement initiatives in compliance with applicable regulatory requirements and quality standard

The Methods Transfer & Validation Specialist Microbiology is responsible for planning executing and documenting microbiological method transfers validations verifications and continuous improvement initiatives in compliance with applicable regulatory requirements and quality standard

Manufacturing Support Specialist to support manufacturing operations by managing controlled documentation coordinating Engineering Change Orders (ECOs) and assisting with continuous improvement initiatives in a highly regulated FDA and ISO environment.Key ResponsibilitiesSupport manuf

Manufacturing Support Specialist to support manufacturing operations by managing controlled documentation coordinating Engineering Change Orders (ECOs) and assisting with continuous improvement initiatives in a highly regulated FDA and ISO environment.Key ResponsibilitiesSupport manuf

Planner to provide on-site support for one of our clients a global leader in medical technology located in Cayey Puerto Rico. The Planner is responsible for supporting supply chain and manufacturing planning activities to ensure material availability inventory optimization and uninter

Planner to provide on-site support for one of our clients a global leader in medical technology located in Cayey Puerto Rico. The Planner is responsible for supporting supply chain and manufacturing planning activities to ensure material availability inventory optimization and uninter

Validation Specialist with a strong knowledge of injection molding processes to support the development execution and documentation of validation activities (Protocols Tests Reports). Familiarized with IQ OQ and PQ validation phases for molds and equipment.IQ: Confirmation of Drawings

Validation Specialist with a strong knowledge of injection molding processes to support the development execution and documentation of validation activities (Protocols Tests Reports). Familiarized with IQ OQ and PQ validation phases for molds and equipment.IQ: Confirmation of Drawings

We are seeking a Senior Data Scientist to collaborate with cross-functional business partners including Commercial Insights Manufacturing Supply Chain Engineering Data teams external vendors service owners and IS partners. This role will develop advanced analytical models and actionab

We are seeking a Senior Data Scientist to collaborate with cross-functional business partners including Commercial Insights Manufacturing Supply Chain Engineering Data teams external vendors service owners and IS partners. This role will develop advanced analytical models and actionab

We are seeking a QA Complaints Analyst to establish and maintain quality assurance programs procedures and controls while ensuring that product performance and quality system elements are continuously measured to support improvement initiatives.Duties & Responsibilities:Monitors and t

We are seeking a QA Complaints Analyst to establish and maintain quality assurance programs procedures and controls while ensuring that product performance and quality system elements are continuously measured to support improvement initiatives.Duties & Responsibilities:Monitors and t

We are looking for a qualified Jr. Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing: Validation protocols.Validation reports.SOPs (Standard Operating Procedures).Statistical data analysisRequirementsBachelor in Scien

We are looking for a qualified Jr. Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing: Validation protocols.Validation reports.SOPs (Standard Operating Procedures).Statistical data analysisRequirementsBachelor in Scien

Provide a wide range of work to fully support the manufacturing processes and products. Implement plan and coordinate inter- departmental activities related to process improvements and product support. Responsible for the diverse range of project activities related to process and prod

Provide a wide range of work to fully support the manufacturing processes and products. Implement plan and coordinate inter- departmental activities related to process improvements and product support. Responsible for the diverse range of project activities related to process and prod

We are seeking a Supplier Quality Engineer to support supplier quality component qualification and continuous improvement activities within a regulated manufacturing environment. This position will be responsible for evaluating supplier capabilities monitoring supplier performance add

We are seeking a Supplier Quality Engineer to support supplier quality component qualification and continuous improvement activities within a regulated manufacturing environment. This position will be responsible for evaluating supplier capabilities monitoring supplier performance add

Quality Documentation Specialist with strong expertise in GMP documentation and quality systems. This role blends traditional QA responsibilities with a focus on managing reviewing and controlling documentation to support compliance and operational excellence.Key Responsibilities: Rev

Quality Documentation Specialist with strong expertise in GMP documentation and quality systems. This role blends traditional QA responsibilities with a focus on managing reviewing and controlling documentation to support compliance and operational excellence.Key Responsibilities: Rev

We are seeking a Sr. Associate EHS with a strong technical background in Environmental Health & Safety to support capital projects equipment installations and EHS activities within regulated industrial pharmaceutical biotechnology or manufacturing environments.Requirements Bachelors o

We are seeking a Sr. Associate EHS with a strong technical background in Environmental Health & Safety to support capital projects equipment installations and EHS activities within regulated industrial pharmaceutical biotechnology or manufacturing environments.Requirements Bachelors o

We are seeking a Specialist Quality Complaints to lead and manage product complaint investigations perform data analysis and trending of complaint information to detect signals proactively and take appropriate actions promptly. RequirementsEducation: Doctorate or Masters 2 years of d

We are seeking a Specialist Quality Complaints to lead and manage product complaint investigations perform data analysis and trending of complaint information to detect signals proactively and take appropriate actions promptly. RequirementsEducation: Doctorate or Masters 2 years of d

We are seeking a detail-oriented and technically skilled professional to support laboratory operations by ensuring the accuracy and compliance of laboratory equipment calibration records. The ideal candidate will have experience reviewing calibration data maintaining equipment perform

We are seeking a detail-oriented and technically skilled professional to support laboratory operations by ensuring the accuracy and compliance of laboratory equipment calibration records. The ideal candidate will have experience reviewing calibration data maintaining equipment perform

We are seeking a C&Q Specialist with expertise in execute qualification activities around an OEM-driven retrofit to an existing GMP manufacturing isolator.Responsibilities: Prepare and maintain all commissioning documentation.Coordinate execution with contractor and vendors.Maintain c

We are seeking a C&Q Specialist with expertise in execute qualification activities around an OEM-driven retrofit to an existing GMP manufacturing isolator.Responsibilities: Prepare and maintain all commissioning documentation.Coordinate execution with contractor and vendors.Maintain c

We are seeking an Engineer with experience working with packaging equipment process characterization validation monitoring and optimization techniques and Expertise in identifying and managing Corrective and Preventive Actions (CAPAs) in a GMP-regulated environment .Proficiency in tec

We are seeking an Engineer with experience working with packaging equipment process characterization validation monitoring and optimization techniques and Expertise in identifying and managing Corrective and Preventive Actions (CAPAs) in a GMP-regulated environment .Proficiency in tec

We are seeking a Sr. Specialist QA to support Quality Assurance program acts as the technical specialist. Review and approve product MPs.FUNCTIONS- Approve process validation protocols and reports for mfg. processes.- Represent Quality on incident triage team.- Approve Environmental C

We are seeking a Sr. Specialist QA to support Quality Assurance program acts as the technical specialist. Review and approve product MPs.FUNCTIONS- Approve process validation protocols and reports for mfg. processes.- Represent Quality on incident triage team.- Approve Environmental C

We are seeking a Process Engineer with pharma-medical device experience as well as validations life-cycle experience (write/execute/analyze/close) to support the daily operations:Root cause analysisInvestigation experience for QN/CAPAclosuresExperience with manual and automated system

We are seeking a Process Engineer with pharma-medical device experience as well as validations life-cycle experience (write/execute/analyze/close) to support the daily operations:Root cause analysisInvestigation experience for QN/CAPAclosuresExperience with manual and automated system

We are seeking Sr. Associate MFG Systems with experience in recipe entry in packaging equipment automation assessment to determine the correct parameter for the recipe and experience in Systech System. RequirementsMaster Degree or Bachelor Degree and 2 years of Engineering experience

We are seeking Sr. Associate MFG Systems with experience in recipe entry in packaging equipment automation assessment to determine the correct parameter for the recipe and experience in Systech System. RequirementsMaster Degree or Bachelor Degree and 2 years of Engineering experience

To support the installation of several manufacturing solid dosage equipment such as but not limited to:EncapsulatorCheckweigherCompression machineHardness testerEncapsulation machineAuxiliary equipmentMain activities should include:Verification of the equipment installed and configure

To support the installation of several manufacturing solid dosage equipment such as but not limited to:EncapsulatorCheckweigherCompression machineHardness testerEncapsulation machineAuxiliary equipmentMain activities should include:Verification of the equipment installed and configure