Quotient Sciences USA Jobs Careers 2022 – Apply Online for Analytical Scientist I Jobs Vacancy in USA

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Quotient Sciences USA is a great organisation there you can make a good career. Job seekers who are talented and wanted to do jobs at Quotient Sciences USA , then it is a great chance for you because of Quotient Sciences USA jobs opening news has published at Quotient Sciences USA Careers page which is www.quotientsciences.com. There we saw many opportunity for freshers and experience candidates who are interested to do work with Quotient Sciences USA . So now you can be a part of this Current Quotient Sciences USA Hiring in . You can read this Quotient Sciences USA job opening article till the end for now each details.


Quotient Sciences USA Jobs 2022 – Apply Online for Analytical Scientist I Job Vacancy in the USA

Quotient Sciences USA Jobs Opening:- Don’t miss this incredible offer announced for Quotient Sciences USA Careers. Quotient Sciences USA’s latest job applications are being announced for Analytical Scientist I job vacancies. Candidates who look smart, young, dynamic, and experienced professionals against the Quotient Sciences USA Analytical Scientist I positions. Jobs in Quotient Sciences USA. Applicants should apply for this position before the last date.

Quotient Sciences USA Job Vacancy 2022 Details

Name of Recruitment Quotient Sciences USA Recruitment 2022
Job Location Job in Boothwyn
Name of Job Opening Analytical Scientist I Jobs  
Job Type Jobs in Pennsylvania
Salary Range $ 87,742.00 Per Year 

Quotient Sciences USA Jobs Description 2022

Company Overview

Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients.

As a growing and successful business, we employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA.

Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it. People join Quotient Sciences because we are a respected member of the drug development community, driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast.

The Role

  • The position supports functionality of the GV laboratory by cleaning and organizing glassware, chemical waste disposal, stocking lab supplies and maintaining general lab cleanliness.
  • Release and stability testing of drug product.
  • To comply & adhere to Good Manufacturing Practice (GMP) standards.

Main tasks and responsibilities will include:

  • Dispose solvent waste as per the laboratory procedures.
  • Change water in dissolution baths.
  • Monitor and maintain lab cleanliness.
  • Perform and document performance verifications for simple laboratory equipment (balances, pH meters, KF titrators, etc.)
  • Order, stock, and label received laboratory supplies.
  • Conduct release and stability testing for drug product in the Commercial analytical team.
  • Follow analytical test methods, compendial methods, experimental procedures, and SOP’s.
  • Document test results in laboratory notebook, in real-time, and communicate status of test results to Group Leader.
  • Peer review laboratory notebooks.
  • Maintain control of all project-related samples submitted to the laboratory.
  • Carry out duties in compliance with all state and federal regulations and guidelines including FDA, EPA, OSHA, and DEA.  Comply with all company and site policies and procedures.
  • Train on SOPs and company procedures on regular basis and remain up to date with the training curriculum.

 

The Candidate

  • Requires BS degree or equivalent.
  • 0-3 years’ pharmaceutical industry experience.

Company benefits

In return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.

Our Commitment to Diversity & Inclusion

Quotient Sciences are advocates for positive change and conscious inclusion.

We strive to create a diverse Quotient family by remaining committed to the development of our culture, equality, mindset, diversity & inclusion in the workplace.

As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today. All applicants welcome.

If you have any questions or need some support with your application, we’d love to hear from you so contact our friendly team at [email protected]

Apply Now


Quotient Sciences USA Jobs 2022 – Apply Online for Data Entry Coordinator Job Vacancy in USA

Quotient Sciences USA Jobs Opening:- Don’t miss this incredible offer announced for Quotient Sciences USA Careers. Quotient Sciences USA latest job applications are being announced for Data Entry Coordinator job vacancy. Candidates who looking smart, young, dynamic, and experienced professionals against the Quotient Sciences USA Data Entry Coordinator positions. Jobs in Quotient Sciences USA. Applicants should apply for this position on before last date.

Quotient Sciences USA Job Vacancy 2022 Details

Name of Recruitment Quotient Sciences USA Recruitment 2022
Job Location Job in Miami
Name of Job Opening Data Entry Coordinator Jobs  
Job Type Jobs in Florida
Salary Range $ 16.00 Per Year (Not Confirm)

Quotient Sciences USA Jobs Description 2022

Our growing and successful business comprises of over 700 talented individuals globally, in an environment where everybody counts and is instrumental to our success. With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.

People join Quotient Sciences because we are a respected member of the drug development world, specialising in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.

The Role

Responsible for the following data entry associated tasks for their assigned studies: source document retrieval, source data QC, data entry, source document filing, QC of CRF entries, laboratory result tracking, and archiving.

Main Tasks and Responsibilities:

Prepares study binders for source documents as instructed by Data Entry Manager.
Performs QC of all source documents, paper and electronic.
Identifies discrepancies in source documents and works with staff for corrections or explanations.
Evaluates query responses in eSource. May reissue query as necessary and re-train staff as appropriate.
Completes CRFs ensuring data entry timelines are met.
Resolves or escalates queries within the established timelines.
Identifies source document or EDC database issues and promptly communicates them to the Data Entry Manager.
Enters, tracks, and performs QC for Adverse Events and Concomitant Medications.
Performs Adverse Event and Concomitant Medication Count (source vs. eCRF).
Performs QC of 100% of completed CRF entries.
Performs timely lab result tracking as assigned by the Data Entry Manager.
Responsible for the accurate and timely filing of all study-related documents.
Ensures that study binders are ready for monitoring visits.
Provides supervisor a daily update of status for all data entry associated tasks for assigned studies.
Reports protocol deviations promptly.
Archives completed study according to established SOPs and Work Instructions
Performs unscheduled accounting and data QA for lab data transfers as assigned by Data Entry Manager.
Greets visitors and registers their arrival and departure in the Visitor Log located in the reception area.
Assists with all other duties as assigned.

The Candidate

Excellent problem solving and organizational skills
Effective communication skills
Computer proficiency (Windows environment)
High School Diploma or equivalent
Able to assume increasing levels of responsibility and perform effectively
Able to plan, coordinate, organize, and prioritize to meet deadlines
Able to interact successfully with team members and study participants
Self-directed – able to perform with minimal supervision
Thorough in task completion- attention to detail
Able to read and understand protocols

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