Analytical Scientist I (QC)

Quotient Sciences

Posted on: September 23, 2022

Closing: October 23, 2022

Salary: Undisclosed

Position Type: Full Time

Job Description

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

Posted on: September 23, 2022

Closing: October 23, 2022

Salary($): Undisclosed

Position Type: Full Time

Similar Jobs


Fargo, United States

QC Analyst I – Clinical

Aldevron is an industry pioneer with a core competency in manufacturing ...

Fargo, United States

QC Analyst II – Clinical...

Aldevron is an industry pioneer with a core competency in manufacturing ...

Philadelphia, United States

PHL_Quality Account Manager

Our investment is in People who make an impact, drive progress and creat...

Makati, Philippines

Regulatory Affairs Consultant

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headq...