Quality Control Analyst

We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

How You’ll Spend Your Day Perform routine and non-routine chemical testing of commercial, validation and stability samples in accordance to written methodology

Perform qualitative and quantitative analyses using analytical instrumentation such as HPLC; GC, UV/Vis, KF and FTIR.Utilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data Analyze data against approved specifications, notifying management of any OOS and aberrant results

Actively participate in root cause problem solving during laboratory investigations, provide input for effective corrective and preventive actions

Perform routine maintenance on lab equipment, as needed

Perform peer review of laboratory testing, as required

Basic knowledge and understanding of USP, cGMP, and FDA regulations

Create and maintain lab record documentation (notebooks and computer based) according to GMPs and GLPsDemonstrate the philosophy of Right First Time Maintain a clean and safe work environment and follow safety procedures and policies.

Provide feedback on systems and processes to promote continuous improvement and champion selected changes

Grow in the job, accountable for establishing and accomplishing annual personal development goals

Contribute to department and site goals

Communicate clearly and well within a team environment

Participate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives

Shares information with others – keeping management informed and helping department to meet the goals

Actively participate in regular one-on-one meetings with direct manager

Communicate external to the department, where applicable

Collaborate effectively to achieve team and organizational goals

Prioritize assigned work to maximize time and equipment efficiency

Work independently with limited supervision for routine assignments

Troubleshoot problems encountered with methods and instruments - routinely solve, choosing among clearly defined alternatives

Responsible for the accurate, timely and compliant execution of assigned projects, analytical testing and related documentation

Your Skills and Experience Any equivalent combination of education, training, and/or experience that fulfills the requirements of the position will be considered.

Bachelor's in science related discipline (Chemistry is preferred)
Experience in a cGMP laboratory

Also Good to Have How We’ll Take Care of You At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.

When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.

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