## 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.

## Our Team, Your Impact

Role Purpose: Support function which prepares materials, planning for product testing, sample receipt and destruction. May perform less complex analyses. Areas of Impact: Performing analytical analysis May carry out checks on record documentation Sample and inspect incoming printed literature Proof read documents once the inspection has been completed Audit and release the literature in SAP after inspecting/proofreading is complete Job Aspect: Conducting the investigation and providing results Execute stability program and sample staging in stability chambers. Performs complex analysis, inspection, and tests of products Performs a variety of qualitative or qualitative tests on samples using techniques that vary from standard analytical equipment to highly modern and automated instrumentation, aides in maintenance and certification of test instruments and apparatus to ensure compliance Competencies: Experienced, expert, can train new hires Tasks are analytical in nature Requires working knowledge or skills developed through formal training or experience Capabilities / Technical Skills: As per skills matrix per site process Qualifications / Trainings: GxP certification - Internal, based on the site and Job Specific training system Quality / work procedures trainings Education: (Expected level of Education, may be impacted by Technology / Site Complexity) High School diploma required. Bachelors in Chemical, Pharmaceutical or Biological field a plus.

## How You’ll Spend Your Day

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Perform and oversee complex chemical and instrumental testing activities in accordance with approved methods and GMP requirements.
Ensure the accuracy, integrity, and reliability of analytical results and laboratory documentation.
Utilize and maintain laboratory information systems (LIMS) and electronic laboratory records.
Support the calibration, qualification, validation, and maintenance of laboratory equipment and instruments.
Manage laboratory inventory, reagents, reference standards, and consumables.
Independently troubleshoot analytical issues, method performance concerns, and laboratory deviations.
Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results and support timely resolution.
Participate in root cause analysis investigations and implementation of corrective and preventive actions (CAPAs).
Review analytical data and ensure compliance with GMP requirements, procedures, and data integrity standards.
Provide technical guidance and support to analysts on testing methodologies and laboratory best practices.
Coach, train, and assess analyst competency to ensure high-quality laboratory performance.
Drive continuous improvement initiatives to enhance laboratory efficiency, compliance, and productivity.
Support method development, optimization, verification, and transfer activities where required.
Assist in the implementation, qualification, and adoption of new analytical technologies and laboratory systems.
Collaborate with cross-functional teams on projects, investigations, validations, and quality initiatives.
Prepare and review technical reports, laboratory records, and investigation documentation.
Perform additional duties as assigned by Quality Control management.

## Your Skills and Experience

Experience working in a GMP pharmaceutical or other regulated laboratory environment.
2 to 4 years of experience in environmental monitoring, water testing, or microbial identification.
Familiarity with laboratory investigations, quality systems, and regulatory requirements.
Experience using LIMS and other electronic laboratory management systems.
Proven experience in troubleshooting, root cause analysis, and continuous improvement initiatives.
Experience supporting CAPA implementation and laboratory process optimization.
Previous experience coaching, mentoring, or training laboratory personnel.

## Also Good to Have

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Degree, Diploma, or Advanced Level qualification in a Science-related discipline.
Strong English communication, comprehension, and technical documentation skills.
Proficiency in Microsoft Office applications and accurate data recording practices.
Strong numerical, analytical, and problem-solving capabilities.
Excellent attention to detail and commitment to data integrity.
Ability to operate laboratory instruments and analytical equipment accurately.
Ability to work effectively under pressure and manage multiple priorities.
Strong teamwork, communication, and collaboration skills.

## 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.

## Already Working @Teva?

Make sure to apply through our internal career site on Twist—your one-stop shop for career development

## 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.

Chemist (Quality Control)

Job Description