Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

Senior Calibration Chemist

Under the direction of the functional leader performs various activities to maintain all analytical instrumentation and ensure their accuracy and GMP compliance.

How you’ll spend your day

Perform precision repairs on complex analytical instruments utilized in the Laboratory.

Coordinate external service technicians as required.

Ensure adequate supply parts are available to ensure testing proceeds with minimal interruption.

Perform requalification after repair (as needed)

Assist onsite Metrology Group with the above duties.

Perform preventative maintenance and Qualification on analytical instruments to minimize unexpected downtime.

Follow Preventative Maintenance procedures as described in the respective SOP.

Use due diligence to monitor and replace/repair any other parts where which may hinder the proper function of the instrument.

Ensure adequate supply parts are available to ensure testing proceeds with minimal interruption.

Assist onsite Metrology Group with the above duties.

Audit PM/Qualification documents produced by onsite metrology group and track RFT statistics to develop improvement strategies.

Monitor costs of maintaining instrumentation and provide feedback to promote and implement cost effective procedures while maintaining GMP compliance.

Monitor repair, service and maintenance costs of all analytical instrument

Implement cost saving measures or procedures while maintaining GMP compliance.

Create and maintain SOPs for the qualification of analytical instruments and ensure qualification intervals are adhered to and documented.

Ensure qualification intervals are adhered to and documented as per SOP

Maintain the LIMS database to track all instrument PM and qualification intervals.

Review and revise SOPs to keep them up to date with current practices.

Review laboratory testing needs when determining qualification procedures.

Fully implement new technology or instrumentation in the laboratory to ensure GMP compliance.

Review manufacturer documents and instrument manuals to determine PM and qualification procedures.

Maintain communication with the manufacturer/vendor to obtain a full understanding of the functionality of the technology

Create SOPs for the PM/Qualification of new technology.

Liaise with IT Department, Engineering Department, Maintenance Department, Lab Management, Manufacturer/Vendor, EH&S and other contacts to ensure all facets of implementation are performed.

Coordinate and follow up on any tasks which may hinder/delay the implementation of the new technology/instrumentation

Lead the onsite Metrology Group by encouraging critical thinking and adhering to assigned timelines.

Assist direct supervisor with the coordination and implementation of all or part of unique projects in the QC Laboratory

Assist direct supervisor with monitoring the Quality, RFT, Compliance and Process Confirmation of on site Metrology Group and actively promote quality improvements

Liaise with IT Department, Engineering Department, Maintenance Department, Lab Management, Manufacturer/Vendor, EH&S and other contacts to ensure all facets of implementation are performed.

Coordinate and follow up on any tasks which may hinder/delay the implementation of the project

Other duties as assigned

Your experience and qualifications

University Degree in Chemistry, Chem. Eng., or other related discipline

5+ years of relevant experience.

Advanced technical knowledge and experience with a wide variety of analytical instrumentation employed in a pharmaceutical laboratory

Progressive experience in laboratory instrument trouble shooting, repair, maintenance and qualification procedures

Exhibit good written and verbal communication skills in order to:

Interact with a variety of Teva management to establish and maintain important business relationships

Provide technical training, guidance and advice to others on laboratory instrumentation techniques and operation.

Knowledge of SAP, LabWare LIMS, Document Management System, MS Office, Lotus Notes, Web based applications suitable for QC Lab environment.

Analytical methods and techniques common to QC Lab

GMP, cGMP, ICH and other requirements as it relates to instrument qualification and validation.

Budgets, spending requirements, regulations and limitations

Key measurements to support business such as customer service, cycle time, costing, etc.

Strong organizational and time management skills

Ability to work well under pressure in a stressful and fast paced working environment

Required to work independently and follow through on assignments/instructions/tasks with minimal supervision/direction

Already Working @TEVA?

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.