Job Description

Who We Are

We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us. We\'re Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world and we currently have a fantastic opportunity for a Chemistry Analyst to join our team on a Full Time, 12 Month Fixed Term Contract in Runcorn.

At Teva Runcorn, we develop, manufacture and market innovative and affordable medicines, specialising in sterile liquid products mainly used for treating respiratory conditions using Blow-Fill-Seal technology as well as injectable Combination Products such as our MS treatment Copaxone.

A Day In The Life Of A Chemistry Analyst

As a Chemistry Analyst you will carry out Product analysis in order to supply quality products to customers and meet department objectives.

Key Responsibilities:

• Test and analyse bulk and finished product using the correct procedures in compliance with cGLP, cGMP, Health and safety, SOPs and environmental and regulatory requirements.
• Working in a fast paced environment comprising of both basic lab-work and the use of complex chemical testing equipment.
• Deliver high customer service to all customers by testing bulk and finished product in an efficient and timely manner.
• Carry out the review of test data and analysis to make sure that product specifications are met.
• Process, maintain and archive all QC documentation, right first time, i.e. correct and in full, in order to achieve customer service and GMP.
• Establish performance/development goals. Maintain training records accurately, ensuring compliance with regulatory and business standards.
• Monitor and purchase laboratory consumables ensuring availability for timely testing of all samples.
• Ensure performance of instrument maintenance and calibration checks.

Who We Are Looking For

Do you have?

Ideally a degree in a relevant discipline and/or position specific experience

Working lab experience ideally before but should have experience through education

Pharmaceutical experience operating to regulatory standards is desirable

Understanding of cGMP/GLP/Regulatory/Health and safety- desirable

Good knowledge of Laboratory instrumentation (such as FT-IR, UV-Vis, HPLC, TOC and DSC)

Are you?

A good communicator and team worker with the ability to deliver high performance standards relating to Quality, Safety, cost and customer service

Someone who has excellent attention to detail

Able to follow procedures and processes closely

If so - we would love to hear from you!

Working Hours

Shift work 6am-6pm, working one weekend every other week. 7 shifts over a 2 week period.

Shift allowance of an additional 19% of your base salary earnings.

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

The deadline for internal applications will close on Monday 2nd October 2023 #TJ

Teva\'s Equal Employment Opportunity Commitment

At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.

Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That is why we are constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice.

Teva Pharmaceuticals