Sr Chemist [Quality Control]
Date:
Feb 3, 2026
Location:
Zejtun, Malta, ZTN 3000
Company:
Teva Pharmaceuticals
Job Id:
66288
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
The opportunity
This role offers the opportunity to work at the heart of the QC laboratory, performing a blend of hands‑on analytical testing and advanced problem‑solving. The successful candidate will develop expertise in complex chemical and instrumental analyses, work with modern QC systems such as LIMS, Empower, LabX, and IDIS, and contribute to critical processes such as OOS/OOT investigations, CAPAs, and method troubleshooting. Beyond routine testing, the position provides the chance to mentor junior analysts, support onboarding, and assess competency—building leadership skills while acting as a technical reference point within the team. With involvement in cross‑functional improvement projects, implementation of new technologies, and continuous method optimization, the candidate will play a key role in driving laboratory excellence, enhancing efficiency, and strengthening GMP compliance. This is a dynamic opportunity for someone who wants to grow technically, contribute meaningfully to laboratory operations, and shape the future of QC practices.
How you’ll spend your day
The selected candidate will spend their day sampling and testing raw materials, intermediates, and finished products in line with pharmacopoeial standards, company procedures, and GMP requirements. While performing routine analytical work, they will also act as a technical leader by mentoring junior analysts, troubleshooting laboratory issues, and supporting continuous improvement initiatives. Their role bridges hands‑on testing with expert guidance, ensuring high-quality results, compliance, and smooth daily operations within the QC laboratory.
Your experience and qualifications
Skills:
Strong written and spoken English
Proficient in Microsoft Office
Solid mathematical ability
Works well under pressureHigh accuracy and attention to detail
Skilled in data calculation and analysis
Proficient in analytical techniques and laboratory equipment
Strong understanding of GMP and data integrity principles
Able to troubleshoot complex analytical and instrumentation issues
Sound scientific judgment and decision‑making
Demonstrated leadership in training and mentoring
Experience driving laboratory improvements
Able to work independently on complex analytical methods
Strong teamwork and collaboration skills
Experience:
4-6 years of experience in a QC laboratory within a regulated environment.
Experience supporting investigations and method remediation activities.
Qualifications:
A degree in Science subjects or a diploma in Applied Science or 2 Advanced levels in Science subjects.
Proficient in Microsoft Office
Solid mathematical ability
Works well under pressureHigh accuracy and attention to detail
Skilled in data calculation and analysis
Proficient in analytical techniques and laboratory equipment
Strong understanding of GMP and data integrity principles
Able to troubleshoot complex analytical and instrumentation issues
Sound scientific judgment and decision‑making
Demonstrated leadership in training and mentoring
Experience driving laboratory improvements
Able to work independently on complex analytical methods
Strong teamwork and collaboration skills
Experience:
4-6 years of experience in a QC laboratory within a regulated environment.
Experience supporting investigations and method remediation activities.
Qualifications:
A degree in Science subjects or a diploma in Applied Science or 2 Advanced levels in Science subjects.
Enjoy a more rewarding choice
•Health Insurance
•Life Insurance
•Performance Bonus
•Personal Growth (Internal Training/Training Platform, certified courses, access to Linked In Learning etc.)
•Internal Career Opportunities
•Free on-site medical services
•Company Car Park Facility
Make a difference with Teva Pharmaceuticals
Reports To
In process of validation
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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.
