method

Full TimeTitle: Method Transfer SpecialistLocation: OnsiteLength of Contract: 6 monthsPosition Description:THE METHOD TRANSFER SPECIALIST IS RESPONSIBLE FOR THE SEAMLESS TRANSITION OF ANALYTICAL METHODS BETWEEN LABORATORIES TO THE BARCELONETA FACILITY. THIS ROLE ENSURES THAT ALL ANALYTICAL METHODS FOR BIOTECHNOLOGICAL PRODUCTS ARE ROBUST, VALIDATED, AND...

The Incoming Method Transfer Specialist is responsible for coordinating, executing, and documenting method transfer activities related to incoming materials, components, and raw materials used in regulated manufacturing operations. This role ensures that specifications, testing strategies, supplier methods, and material controls are successfully transferred,...

Company DescriptionQRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.Log on now to our website / to learn more about our services and solutions!Job DescriptionThe Incoming Method Transfer Specialist is responsible for coordinating, executing, and...

Company DescriptionQRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.Log on now to our website / to learn more about our services and solutions!Job DescriptionThe Methods Transfer - Validation Specialist is responsible for planning, executing, and...

Company DescriptionQRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.Log on now to our website / to learn more about our services and solutions!Job DescriptionThe Methods Transfer - Validation Specialist is responsible for planning, executing, and...

The Methods Transfer - Validation Specialist is responsible for planning, executing, and documenting analytical method transfers, validations, verifications, and method improvement initiatives in compliance with regulatory requirements. This role ensures analytical methods are robust, reproducible, and suitable for their intended use across internal and...

*Summary*We are seeking a Specialist in Quality Control to support quality and scientific operations in a highly regulated pharmaceutical environment. The ideal candidate has a scientific or engineering background and experience in laboratory testing, method validation, and quality processes. This role requires strong technical writing, data analysis, and...

*Overview*Doctorate or Masters + 2 years of directly related experience or Bachelors + 4 years of directly related experience or Associates + 8 years of directly related experience or High school/GED + 10 years of directly related experience.Preferable Scientific Background (Science or Engineering) with experience in Pharmaceutical Industry, Quality Control,...

OverviewDoctorate or Masters + 2 years of directly related experience or Bachelors + 4 years of directly related experience or Associates + 8 years of directly related experience or High school/GED + 10 years of directly related experience.Preferable Scientific Background (Science or Engineering) with experience in Pharmaceutical Industry, Quality Control,...

Under general supervision, responsible for one or more of the following activities in Quality Control including analytical testing, characterization, method development, and sample and data management.Requisitos:Bachelor's degree in chemistry or microbiology.

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities:Supports equipment...

mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network...

MÎRUS CONSULTING GROUP IS A LOCAL COMPANY BASED IN HUMACAO, PUERTO RICO THAT PROVIDES COMPUTER SYSTEM VALIDATION AND INFORMATION TECHNOLOGY CONSULTING SERVICES TO PHARMACEUTICAL COMPANIES AND OTHER ORGANIZATIONS ACROSS THE ISLAND AND PARTS OF THE UNITED STATES. ITS SERVICES INCLUDE THE ASSESSMENT AND VALIDATION OF AUTOMATION EQUIPMENT, NETWORK...

Job Title: Quality Control Specialist (Regulated Industry) – *******Location: Puerto Rico (100% Onsite)Positions Available: 3Duration: Approximately 6 MonthsWork Schedule: Availability to work administrative and non-standard shiftsEligibility: Open to Puerto Rico residentsPosition SummaryOur client is seeking a Quality Control Specialist to support...

Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources.Requisitos:-Doctorate OR -Masters + 2 years of directly related experience...

Temporary Job - initially for 6 months - Working Shift-1st ShiftWhat are the top 3 things you are looking for in a candidates experience:1. Computer system validation, equipment validation, Test method validation2. Manufacturing Documentation changesJOB DESCRIPTIONResponsibilities may include the following and other duties may be assigned. Provides oversight...

mîrus Consulting Group is a Puerto Rico based technical services firm headquartered in Humacao. The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States. Its services include the assessment and validation of...

mîrus Consulting Group is a Puerto Rico based technical services firm headquartered in Humacao. The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States. Its services include the assessment and validation of...

We're looking for qualified CDL Drivers who are interested in taking the next step in their career and become owner operators. Our Lease program is setup to allow you to make great money and be your own boss. Call ************ to apply now.Qualifications * 6 Months Class A Driving Experience NEEDED * Take home $****+ weekly * $0 Money down * NO CREDIT CHECK...

*Overview*Under general supervision, this role is responsible for one or more of the following activities in Quality Control: analytical testing, characterization, method development, and/or sample and data management in a regulated medical manufacturing facility.*Responsibilities** Performs routine laboratory procedures* May perform aseptic aliquot ting,...