Chemist (Quality Control)

We Are TevaWe'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 ImpactRole 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 DayPerform 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 ExperienceExperience 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 HaveDegree, 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 collaborati