The Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated pharmaceutical environment. This role ensures compliance with cGMP regulations through the planning execution and documentation of vali

The Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated pharmaceutical environment. This role ensures compliance with cGMP regulations through the planning execution and documentation of vali

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Full Time

The Microbiology Analyst I is responsible for performing routine microbiological testing and laboratory activities in support of quality control manufacturing and compliance requirements. This entry-level role provides hands-on experience in a regulated laboratory environment and offe

The Microbiology Analyst I is responsible for performing routine microbiological testing and laboratory activities in support of quality control manufacturing and compliance requirements. This entry-level role provides hands-on experience in a regulated laboratory environment and offe

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Full Time

We are searching Specialist Quality Control with experience in deviation microbiology HPLC and analytical methods. RequirementsDoctorate or Masters 2 years of directly related experience or Bachelors 4 years of directly related experience orAssociates 8 years of directly related ex

We are searching Specialist Quality Control with experience in deviation microbiology HPLC and analytical methods. RequirementsDoctorate or Masters 2 years of directly related experience or Bachelors 4 years of directly related experience orAssociates 8 years of directly related ex

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Investigation Specialist for Solid Dosage will be responsible for performing thorough detailed and timely investigations and generation of high quality and timely investigation reports. Responsibilities: Understanding of the investigation process as it applies to manufacturing issues

Investigation Specialist for Solid Dosage will be responsible for performing thorough detailed and timely investigations and generation of high quality and timely investigation reports. Responsibilities: Understanding of the investigation process as it applies to manufacturing issues

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Full Time

QRC Group is seeking a Process Development Scientist with:Experience preparing syringes and vials with cosmetic particle or solution defects for developmental studies equipment characterization training activities and commercial equipment setup.Experience using laboratory equipment an

QRC Group is seeking a Process Development Scientist with:Experience preparing syringes and vials with cosmetic particle or solution defects for developmental studies equipment characterization training activities and commercial equipment setup.Experience using laboratory equipment an

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Full Time

The Industrial Mechanic will perform basic tasks associated with the installation maintenance and repairs of manufacturing and packaging equipment. Able to identify locates and diagnoses failure replaces defective components and performs basic troubleshooting using standard electronic

The Industrial Mechanic will perform basic tasks associated with the installation maintenance and repairs of manufacturing and packaging equipment. Able to identify locates and diagnoses failure replaces defective components and performs basic troubleshooting using standard electronic

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Full Time

We are seeking a Microbiologist Analyst to support the current Equipment Validation process:Analyzes Microbiological and Environmental test data and utilizes professional judgment to decide on appropriate responses to related events departures validations etc.Supports manufacturing ac

We are seeking a Microbiologist Analyst to support the current Equipment Validation process:Analyzes Microbiological and Environmental test data and utilizes professional judgment to decide on appropriate responses to related events departures validations etc.Supports manufacturing ac

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Qrc Group

Full Time

The Accounting Clerk calculates prepares and processes invoices bills payroll reports and other financial records. Perform other duties specific to the company as well a wide range of basic office tasks. Provides excellent internal and external customer service.Duties:Biweekly collect

The Accounting Clerk calculates prepares and processes invoices bills payroll reports and other financial records. Perform other duties specific to the company as well a wide range of basic office tasks. Provides excellent internal and external customer service.Duties:Biweekly collect

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Full Time

The Senior Manufacturing Engineer will apply scientific knowledge engineering knowledge mathematics and ingenuity to lead moderately and/or high complex projects with little to no supervision.Tasks:Runs studies and qualification/validations on the line as needed. Writes protocols and

The Senior Manufacturing Engineer will apply scientific knowledge engineering knowledge mathematics and ingenuity to lead moderately and/or high complex projects with little to no supervision.Tasks:Runs studies and qualification/validations on the line as needed. Writes protocols and

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Qrc Group

Full Time

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

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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

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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

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Qrc Group

Full Time

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

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Full Time

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

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Qrc Group

Full Time

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

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Full Time

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

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Full Time

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

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Qrc Group

Full Time

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

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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

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Full Time

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

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