Quality Control Chemist

Date: Mar 30, 2026

Location:

Zejtun, Malta, ZTN 3000

Company: Teva Pharmaceuticals

Job Id: 67095

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

Support laboratory operations by preparing materials, planning product testing, managing sample receipt and destruction, and performing analytical testing, including more complex analyses and inspections.

Perform analytical testing and inspection activities on products and materials
Review and verify documentation for accuracy and compliance
Support stability programs and sample management processes
Ensure quality and compliance in laboratory and documentation workflows

How You’ll Spend Your Day

Perform analytical testing using standard and advanced laboratory instrumentation
Conduct inspection and proofreading of printed materials and documentation
Audit and release materials in SAP following inspection and verification
Execute stability programs, including sample staging and monitoring
Investigate deviations and provide accurate analytical results
Maintain laboratory equipment and support calibration and certification activities
Ensure all activities are documented accurately and in compliance with GxP standards
Support and train junior team members where required

Your Skills and Experience

Skills

Strong analytical and laboratory testing skills
Ability to work independently and handle more complex tasks
Knowledge of GMP/GxP requirements and documentation practices
Attention to detail in inspection and proofreading activities
Good organizational and documentation skills
Ability to train and mentor less experienced staff

Experience

Previous experience in a laboratory or quality control environment
Experience with analytical equipment and testing methods
Exposure to stability studies, documentation review, or inspection activities is an advantage

Also Good to Have

High School Diploma required
Bachelor’s degree in Chemical, Pharmaceutical, Biological, or related field is an advantage
Experience with SAP or similar systems
Familiarity with stability programs and sample lifecycle management
Experience in deviation investigations and audit processes
Exposure to regulated environments such as pharmaceutical manufacturing

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.