Analytical Chemist

at  Pharmaron

WE ARE LOOKING FOR:

Pharmaron is currently looking to recruit an Analytical chemist who is enthusiastic and highly motivated to work at their Rushden facility in the Chemistry Quality Control Department. You will have a sound basic theoretical understanding of a range of analytical techniques primarily chromatographic and spectroscopic.

After a structured period of training the successful candidate will be required to carry out analyses on a diverse range of chemical compounds, generate and provide first line interpretation of the resulting data and preferably be able to defend the interpretation to senior QC analysts and internal Clients. You will be expected to produce analytical reports compliant with Pharmaron QA systems. You will ensure that the instrumentation under your charge is maintained, operationally available, as far as is reasonably practicable at all times, and that there is an adequate supply of materials to meet QC operational requirements. You will have a can-do attitude always looking for ways to support the business outside of your immediate job specification. 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!

Key roles and responsibilities:

• Have a good theoretical understanding of analytical techniques and processes
• Carry out quality control (QC) analysis of materials manufactured by custom synthesis teams as required
• Perform QC analysis of materials on stability as required
• Be able to interpret analytical results and describe and explain them to a wider audience
• Maintain accurate and clear laboratory records
• Maintain QC instruments in good working order and report any faults promptly
• Participate in verification/validation of analytical methods, drafting method verification protocols/reports, and controlled analysis documents
• Prepare out-of-specification (OOS) and deviation documentation when necessary
• Participate in the validation/qualification of laboratory equipment as required
• QC release raw materials from Quarantine for use in GMP manufacture
• Carry out QC review of analytical data

Requirements:

• Degree in Chemistry, or relevant experience
• Good theoretical grounding of chromatographic and spectroscopic techniques
• Good written and verbal communication skills
• Computer literate
• Ability to work with minimum supervision and as part of a team
• Conscientious and meticulous in laboratory and written work
• Good time management skills and ability to work to tight deadlines
• Proven ability to problem solve
• Willing to get involved with new ideas and initiatives

Desirable requirements

• Experience as a practising analyst, particularly with chromatographic and spectroscopic techniques.
• Experience in data evaluation using spreadsheet and statistical tools.
• An appreciation of quality/regulatory standards and quality systems - in particular the relationship of the MHRA with the pharmaceutical industry.

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.

Based in Northamptonshire, our Rushden site is a centre of excellence for Radiolabelled Sciences incorporating both Metabolism (which includes Clinical Metabolism, Pre-clinical ADME, In vitro and DDI services, Large Molecule Metabolism, Environmental Fate, Plant Metabolism and Metabolite Identification) in addition to Chemistry (which includes API and IMP manufacture). We offer our employees a supportive teamwork environment, enabling them to develop and liberate their true potential.

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

Why Should You Apply?

• This is an opportunity for you as Quality Control professional 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 of Chemistry.
• 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.

After a structured period of training the successful candidate will be required to carry out analyses on a diverse range of chemical compounds, generate and provide first line interpretation of the resulting data and preferably be able to defend the interpretation to senior QC analysts and internal Clients. You will be expected to produce analytical reports compliant with Pharmaron QA systems. You will ensure that the instrumentation under your charge is maintained, operationally available, as far as is reasonably practicable at all times, and that there is an adequate supply of materials to meet QC operational requirements. You will have a can-do attitude always looking for ways to support the business outside of your immediate job specification. 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

Key roles and responsibilities:

• Have a good theoretical understanding of analytical techniques and processes
• Carry out quality control (QC) analysis of materials manufactured by custom synthesis teams as required
• Perform QC analysis of materials on stability as required
• Be able to interpret analytical results and describe and explain them to a wider audience
• Maintain accurate and clear laboratory records
• Maintain QC instruments in good working order and report any faults promptly
• Participate in verification/validation of analytical methods, drafting method verification protocols/reports, and controlled analysis documents
• Prepare out-of-specification (OOS) and deviation documentation when necessary
• Participate in the validation/qualification of laboratory equipment as required
• QC release raw materials from Quarantine for use in GMP manufacture
• Carry out QC review of analytical dat