Aequor

Responsibilities: Reviews patient eligibility Reviews patient level and cumulative data per the data review plan across a study and coordinates with the medical lead for study level review Reviews protocol deviations Reviews safety data SAE repo

Responsibilities: Reviews patient eligibility Reviews patient level and cumulative data per the data review plan across a study and coordinates with the medical lead for study level review Reviews protocol deviations Reviews safety data SAE repo

Fully Onsite: 4/10 Schedule (4 days on 3 days off 10hrs/day) Job Summary: The Associate Quality Control supports sample management and laboratory activities within the Quality Control department. This role is responsible for the receipt handling tracking storage and disposal of samp

Fully Onsite: 4/10 Schedule (4 days on 3 days off 10hrs/day) Job Summary: The Associate Quality Control supports sample management and laboratory activities within the Quality Control department. This role is responsible for the receipt handling tracking storage and disposal of samp

Description: Independently performs the tasks of the production operation specific to aseptic cleaning. Maintains batch record documentation and logs as required by corporation and regulatory agencies. Must be able to perform cleaning and sanitizing of production equipment and classif

Description: Independently performs the tasks of the production operation specific to aseptic cleaning. Maintains batch record documentation and logs as required by corporation and regulatory agencies. Must be able to perform cleaning and sanitizing of production equipment and classif

Job Description: Quality Compliance Associate Large Pharmaceutical Company is searching for a Quality Compliance Associate to join the Quality Compliance team in Irvine CA! In this role you will: Co-Lead internal audits for the sites compliance to GMP regulati

Job Description: Quality Compliance Associate Large Pharmaceutical Company is searching for a Quality Compliance Associate to join the Quality Compliance team in Irvine CA! In this role you will: Co-Lead internal audits for the sites compliance to GMP regulati

Sr. Desktop Engineer Onsite in Sarasota FL Contract Role 6 months with Possible Extension Role Requirements & Candidate Profile: Availability: Must be local to the area and available to start immediately. Core Expertise: Senior-level Desktop Engineering background with strong Prin

Sr. Desktop Engineer Onsite in Sarasota FL Contract Role 6 months with Possible Extension Role Requirements & Candidate Profile: Availability: Must be local to the area and available to start immediately. Core Expertise: Senior-level Desktop Engineering background with strong Prin

Overview We are seeking a Biosafety Officer who will be responsible for protecting the Institutes employees contractors visitors the general public and the environment from potential exposures to Select Agents and Toxins; and to ensure that the Institute maintains full compliance wit

Overview We are seeking a Biosafety Officer who will be responsible for protecting the Institutes employees contractors visitors the general public and the environment from potential exposures to Select Agents and Toxins; and to ensure that the Institute maintains full compliance wit

Job Title: Manager Congress Strategy & Orchestration (CS&O) Location: East Hanover NJ (Hybrid) Duration: 7 months Pay Rate: *** - ***/hr Job Description: The Manager Congress Strategy & Orchestration (CS&O) is a headquarters-based role responsible for supporting the orchestration an

Job Title: Manager Congress Strategy & Orchestration (CS&O) Location: East Hanover NJ (Hybrid) Duration: 7 months Pay Rate: *** - ***/hr Job Description: The Manager Congress Strategy & Orchestration (CS&O) is a headquarters-based role responsible for supporting the orchestration an

Actual Job Title: Reagent Manufacturing Associate1st Shift : 5:30am-2:00pmJOB RESPONSIBILITIES:Perform Entry level operations (Sorting Aliquoting Labware cleaning)Reliable inspection of small beadsPack and sample reagent beads coming out of the freeze-drierMaintain work area in compli

Actual Job Title: Reagent Manufacturing Associate1st Shift : 5:30am-2:00pmJOB RESPONSIBILITIES:Perform Entry level operations (Sorting Aliquoting Labware cleaning)Reliable inspection of small beadsPack and sample reagent beads coming out of the freeze-drierMaintain work area in compli

Job Title: Automation SpecialistLocation: South San Francisco CA 94080 (on-site)Duration: 12 months contractTerms: Contract W2Required skillsMust have experience in automation of cell cultureHands-on experience in Laboratory automation / liquid handlingExperience operating programming

Job Title: Automation SpecialistLocation: South San Francisco CA 94080 (on-site)Duration: 12 months contractTerms: Contract W2Required skillsMust have experience in automation of cell cultureHands-on experience in Laboratory automation / liquid handlingExperience operating programming

Duties Responsibilities for this position would focus on animal studies including monitoring dosing and animal necropsy and organ collection. The individual will be expected to work with infectious and/or bio-hazardous reagents and material. The individual is also going to be involve

Duties Responsibilities for this position would focus on animal studies including monitoring dosing and animal necropsy and organ collection. The individual will be expected to work with infectious and/or bio-hazardous reagents and material. The individual is also going to be involve

Role: Administrative Assistant and Front Desk Receptionist Duration: 12 month contract Schedule: Monday - Friday ( Day shift) on site. Required Experience: 5 years of Administrative / Reception experience Strong

Role: Administrative Assistant and Front Desk Receptionist Duration: 12 month contract Schedule: Monday - Friday ( Day shift) on site. Required Experience: 5 years of Administrative / Reception experience Strong

Scientist Analytical Sciences & Technology1 Year Contract with high possibilities of extensionEast Syracuse NYQualifications:Education/Experience/ Licenses/Certifications:B.S in Biology Chemistry Biotechnology or equivalent area of related study with 2-5 yrs. industry experience in bi

Scientist Analytical Sciences & Technology1 Year Contract with high possibilities of extensionEast Syracuse NYQualifications:Education/Experience/ Licenses/Certifications:B.S in Biology Chemistry Biotechnology or equivalent area of related study with 2-5 yrs. industry experience in bi

Clinical Laboratory Scientist/Lab ManagerJob DescriptionGolden Star Labs is leading the industry in science and innovation to better support communities and institutions testing needs across the United States. We are looking for an experiencedCLS with a microbiology or generalist clas

Clinical Laboratory Scientist/Lab ManagerJob DescriptionGolden Star Labs is leading the industry in science and innovation to better support communities and institutions testing needs across the United States. We are looking for an experiencedCLS with a microbiology or generalist clas

Provides robust and efficient support of information flows in Supply Chain Management (SCM) relevant business systems. The individual will leverage their expertise and work experiences as well as industry best practices in successfully implementing solutions primarily in the planning

Provides robust and efficient support of information flows in Supply Chain Management (SCM) relevant business systems. The individual will leverage their expertise and work experiences as well as industry best practices in successfully implementing solutions primarily in the planning

Role and Responsibilities The Contract QA Specialist Validation / Qualification is responsible to provide quality oversight and ensure that validation and qualification activities conducted at Lupin Somerset are in compliance with FDA regulations guidance and other recognized ind

Role and Responsibilities The Contract QA Specialist Validation / Qualification is responsible to provide quality oversight and ensure that validation and qualification activities conducted at Lupin Somerset are in compliance with FDA regulations guidance and other recognized ind

Manufacturing Technical Support Scientist Level II We are looking for an experienced Scientist to design and develop experimental studies and create associated study protocols in support of investigations and troubleshooting of both products or processes and product or process impr

Manufacturing Technical Support Scientist Level II We are looking for an experienced Scientist to design and develop experimental studies and create associated study protocols in support of investigations and troubleshooting of both products or processes and product or process impr