QA Shopfloor Specialist, Extended day shift
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
As a QA Shopfloor Specialist, you'll be the eyes and ears for quality in production and supportive areas, ensuring the quality, safety and efficacy of pharmaceutical products. This dynamic role offers the chance to directly impact lives by overseeing production processes on the shop floor. You'll collaborate with a skilled team, tackle critical projects, and have the potential to progress within the QA department.
Extended Day Shift: In this role, you will work under a 2-shift system, alternating between morning and evening shifts.
How you’ll spend your day
Conduct shop floor supervision to ensure compliance with GMP regulations and procedures
Observe shop floor operations to ensure aseptic behavior of operators in classified areas
Collaborate with the production manager to resolve GMP observations and initiate quality improvement projects aimed at controlling risks in production processes
Prepare reports on shop floor observations
Review documents as part of oversight
Participate in projects on behalf of QA
Coordinate corrective and preventive actions initiated as a result of various investigations
Your experience and qualifications
HBO/Academic degree in Process Technology, Chemical Engineering, Pharmacy, Microbiology, or Food Technology
Good understanding of quality management principles, FDA, and EU GMP guidelines
Knowledge of aseptic processes and validation is a plus
Fluency in Dutch and English is essential
Excellent communication skills to clearly formulate thoughts, problems, and solutions
A proactive, persuasive, meticulous, and decisive approach
What do we offer?
25 paid holidays
Competitive salary
Shift allowance
A number of health benefits including like Accident Assurance and Income protection
9 weeks of fully paid parenteral leave
Flexible working conditions
Competitive Pension
Fully covered public transport contribution
A very diverse international team
Contact person
Ivo Huijskens - Senior Recruiter Benelux & Nordics
Reports To
Head of Quality Assurance
Already Working @TEVA?
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Pre employment screening
Teva will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process
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.
