Scientific Associate II, Analytical Sciences - 6 Month - Fixed Term Contract

at  Pharmaron

Job Introduction We are looking for:
A Scientific Associate II on a six month fixed term basis to support and perform activities associated with the development, optimization, phase appropriate validation, transfer and application of analytical methodologies suitable for in-process development testing, non-GMP and cGMP release testing of biological products.

At Pharmaron we offer:

• Vibrant and dynamic employment – we are a highly specialised, growth company operating in a critical sector of the economy – our future is strong and exciting!
• Opportunities to develop your skills and yourself – our rapid growth brings greater opportunities for you to learn and grow faster!
• A great team where we all support each other – enjoy your work – after all you spend about a third of your time here!

Requirements:Essential:

• BSc/MSc (or equivalent) in a relevant life sciences field
• Evidence of strong academic or industrial achievement required.
• Knowledge of various Analytical Molecular Biology techniques such as qPCR, ddPCR, Sanger sequencing, Restriction digest and agarose gel electrophoresis

Desirable:

• Relevant industrial experience within the biopharmaceutical or pharmaceutical industry (gene therapy most ideal). Working in analytical development, performing method development, equipment qualification, phase appropriate validation and testing.

Key roles and responsibilities:

• Maintains exemplary standards within the laboratory and facility in compliance with Development, Quality and EHS Policies and Procedures.
• Under minimal analytical supervision supports delivery of internal and Client-based work packages through the delivery and reporting of activities within the analytical laboratories to meet project timelines and in line with policies and procedures. Drives the procurement of stock reagents and consumables and ensures laboratory housekeeping for all work performed.
• Completes all laboratory or batch analysis (non-GMP and/ or GMP) in a timely and compliant manner.
• Under minimal analytical supervision contributes to the preparation and executes a range of documentation including but not limited to development reports, operating procedures, phase appropriate validation, analytical proformas and test records in a timely manner with a right first-time mind set.
• Completes all laboratory or batch analysis and related documentation in a timely and compliant manner.

Our Company: “We are a dynamic, fast-growing company, with an enviable reputation for leading edge science, offering contract research services to some of the world’s leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges”.We believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.We are based in the vibrant city of Liverpool with a world class R&D and manufacturing facility that offers a complete end to end development service. Our 80,000 sq. ft facility houses an established Biologics Department that consists of Analytical and Process Sciences. Our Liverpool site has a remarkable 20 Year Track Record in Biologics Development, which now offer A Fully Integrated Gene Therapy Drug Substance Solution in our state of the art cGMP facility purpose designed for viral vectors with onsite plasmid DNA and renowned analytical capabilities for release and characterisationThe Pharmaron Liverpool Team has consistently delivered biologics programs across all development phases and due to constant growth we are now recruiting a Scientist within our Analytical Sciences department.

• We offer a competitive salary and a progressive and comprehensive suite of employee benefits
• We offer state of the art working environment in our modern Liverpool site
• We offer the opportunity for growth and development and will support funding for relevant training and development programmes

We do more than manufacture batches, we develop medicines!Why Should You Apply?

• This is an opportunity for you as a Scientific Associate II to make a real impact in a highly scientific and regulated environment, demonstrate leadership, ambition and the desire to grow with the department.
• Build and shape your career in an environment that sets and commits to the highest standards.
• To be part of a team who support each other, embrace and solve technical challenges and put excellence at the heart of all that we do.

Pharmaron is a premier R&D service company supporting the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities having established diverse drug R&D service capabilities, ranging from synthetic, medicinal, and analytical chemistry, biology, DMPK, pharmacology, drug safety assessment, radiochemistry and isotopically labelled metabolism, chemical & pharmaceutical development to clinical development. With operations in China, US and UK staffed by over 19,000 employees, Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan, and China

Key roles and responsibilities:

• Maintains exemplary standards within the laboratory and facility in compliance with Development, Quality and EHS Policies and Procedures.
• Under minimal analytical supervision supports delivery of internal and Client-based work packages through the delivery and reporting of activities within the analytical laboratories to meet project timelines and in line with policies and procedures. Drives the procurement of stock reagents and consumables and ensures laboratory housekeeping for all work performed.
• Completes all laboratory or batch analysis (non-GMP and/ or GMP) in a timely and compliant manner.
• Under minimal analytical supervision contributes to the preparation and executes a range of documentation including but not limited to development reports, operating procedures, phase appropriate validation, analytical proformas and test records in a timely manner with a right first-time mind set.
• Completes all laboratory or batch analysis and related documentation in a timely and compliant manner

Our Company: “We are a dynamic, fast-growing company, with an enviable reputation for leading edge science, offering contract research services to some of the world’s leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges”.We believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.We are based in the vibrant city of Liverpool with a world class R&D and manufacturing facility that offers a complete end to end development service. Our 80,000 sq. ft facility houses an established Biologics Department that consists of Analytical and Process Sciences. Our Liverpool site has a remarkable 20 Year Track Record in Biologics Development, which now offer A Fully Integrated Gene Therapy Drug Substance Solution in our state of the art cGMP facility purpose designed for viral vectors with onsite plasmid DNA and renowned analytical capabilities for release and characterisationThe Pharmaron Liverpool Team has consistently delivered biologics programs across all development phases and due to constant growth we are now recruiting a Scientist within our Analytical Sciences department.

• We offer a competitive salary and a progressive and comprehensive suite of employee benefits
• We offer state of the art working environment in our modern Liverpool site
• We offer the opportunity for growth and development and will support funding for relevant training and development programme