## 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

Review and approve/reject printed packaging materials in a timely manner according to the production plan.
Prioritise packaging materials listed in the Exceptions Report and ensure same-day review when entered into SAP.
Review and approve printed packaging material specifications, including Version 1 and non-Version 1 documents.
Sample printed packaging materials upon request.
Compile Certificates of Analysis (CoAs) for printed packaging materials as required.
Prepare Batch Release Certificates (Commercial and Registration), including CoAs, BRCs, and CoCs, prior to Qualified Person (QP) review and within agreed timelines.
Provide clients with commercial batch documentation, including approved certificates, starting material certificates, and manufacturing/packaging batch documentation as specified in Technical Agreements or product specifications.
Coordinate the preparation and distribution of finished product samples, registration documentation, and supporting information required for product registration and business expansion activities.
Act as the primary liaison between clients and internal departments for quality-related queries and requests, ensuring responses are provided within 48 hours.
Perform training on new or updated Standard Operating Procedures (SOPs) and ensure compliance with authorised SOPs at all times.
Maintain and update QA records, databases, and logbooks regularly to support efficient and reliable operations.
Archive and retrieve QA batch documentation, logbooks, and packaging material samples as required.
Participate actively in projects aimed at improving quality assurance processes and departmental performance.
Compile assigned Product Quality Reviews (PQRs) on a monthly basis.
Perform additional duties and responsibilities as required by the department.

## Your Skills and Experience

Excellent attention to detail and accuracy.
Strong customer service orientation.
Effective communication and organisational skills.
Proactive, reliable, and hardworking attitude.
Proficiency in Microsoft Office applications.
Ability to work under pressure and meet strict deadlines.
Strong teamwork and collaboration skills.

Also prefered to have;

Diploma-level education.
Experience in quality assurance, pharmaceutical operations, packaging review, or a related field is considered an asset.

## 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.

Quality Assurance Sr Specialist [Operations Support]

Job Description