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Position background
The Technical Services department within Tjoapack is responsible for the development of various validation and FDA compliant documents for primary and secondary pharmaceutical packaging. Technical documentation includes packaging specifications/protocols and equipment qualifications/validation.
As a member of technical services, you are part of the team that plays a key role in transforming the pharmaceutical supply chain and accordingly (re)packaging medicines to make them timely available for the relevant markets.
We expect that you have a positive mind-set, able to assess the possibilities to produce more efficient and take action on improvement ideas to do so. In this position you will report to the Sr. Director, OpEX and Engineering.
Your responsibilities include
Our offerWe will help you become successful in your new job with a customized development plan. At Tjoapack, we work hard, encourage innovative ideas, and give freedom to work independently.
Place within the organization Tjoapack is a global and independent Contract Packaging Organisation (CPO) of medicines.
We’re located in Etten-Leur, the Netherlands. And since October 2021 we also have a location in Clinton, the United States. With over 30 years of experience in providing packaging solutions for the pharmaceutical industry, we process millions of medicine packages per year for 42 countries in 5 continents.
Tjoapack is a global contract packaging organization (CPO) specializing in primary and secondary pharmaceutical packaging and supply chain management services. We’re dedicated to shaping the future of the pharmaceutical supply chain to be safer and more reliable for our customers and for patients. With more than 30 years of track record in contract packaging, we use our knowledge and experience to offer flexible solutions to our customers challenges and use the latest technologies to continuously improve our operations. We now supply products to over 45 countries across all continents.
We are focused on shaping the future of the pharmaceutical supply chain to make it safer and more reliable for our customers and for patients. The patient is de centre of our supply chain solutions to ensure that our medicines reach the patient on time. With this approach our products are usable, available, traceable, and affordable.
This is one of the reasons why we always strive to continuous improvement and development of new technologies new technologies. Most importantly, our knowledge and experience allow us to offer flexible packaging solutions and supply chain services, advise customers on market regulations and ensure we have the right solution to meet their product requirements.
Your letter of motivation should be in English. Please use the button to apply and address your letter and resume to Samira Houdane, Corporate Recruiter.
Your background, qualification, and skills
Full Time
$101k-120k (estimate)
05/25/2024
07/23/2024
The job skills required for Validation Engineer (2) include Project Management, Written Communication, Initiative, Packaging, etc. Having related job skills and expertise will give you an advantage when applying to be a Validation Engineer (2). That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Validation Engineer (2). Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Validation Engineer (2) positions, which can be used as a reference in future career path planning. As a Validation Engineer (2), it can be promoted into senior positions as a Validation Engineer II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Validation Engineer (2). You can explore the career advancement for a Validation Engineer (2) below and select your interested title to get hiring information.