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Pharmaceutical Specialist

Haarlem, Netherlands

Who we are

Teva is a global pharmaceutical leader and the world's largest generic medicines producer committed to improving health and increasing access to quality Health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development, and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

The opportunity

Are you an ambitious professional who is already familiar with pharmaceutical production processes? Are you someone who enjoys asking questions? Do you find it important to understand the way things work? Get ready for a new challenge in the Pharma industry and join the investigation and improvement team, as a Pharmaceutical Specialist!
What is the goal of the Investigation and Improvement team? They are the brain of the company! The key aim of the team is to investigate any issues in production and find the root cause. They draw up, initiate and execute improvement proposals in response to production deviations. They assess or decide whether production activities should be stopped or adapted. Be part of this dynamic team and take your carrer to the next level! Work between production and the quality department and participate in various projects to improve quality aspects. In this dynamic position every day looks different. If you are creative, likes to be busy and always enjoys something new, then this position is for you!

Your responsibilities

Responsible for pharmaceutical and quality aspects within production, including:

Ensure the improvement, support, testing and control of the activities related to pharmaceutical manufacturing process (bulk production and packaging):

•    Support the production department in case of deviations and quality issues.
•    Assess or decide whether production activities should be stopped or adapted due to a deviation.
•    Make proposals to improve manufacturing methods and products, and to implement developments in manufacturing technology.

Provide substantive and technical support to the Business Unit with regard to quality issues and improvement processes:

•    Monitoring and reporting on (deviations from) the manufacturing processes.
•    Investigate and document observed deviations and complaints.
•    Conduct and document root cause investigations and CAPAs.
•    Drawing up, initiating and executing improvement proposals in response to production deviations, (internal and external) audit observations or as part of continuous improvement.
•    Making recommendations for working conditions, (product) safety and the environment.
•    Participate in various projects to improve quality aspects.
•    Support with Compliance investigations and Audit responses.

Implement and maintain the corporate quality and GMP instructions and ensure adequate protocolling:

•    Reviewing SOPs, manufacturing and validation protocols, Master Batch Records (MBRs)
•    Prepare and review trend reports on manufacturing processes
•    Participate / contribute to projects, changes, CAPAs etc.
•    Knowledge transfer, training of manufacturing personnel or technicians.

Participate in the Tier structures of the Business Units.

Your profile

•    Minimum of a bachelor degree in Pharmacy, Pharmaceutical technology, Bio-Chemistry or any related field
•    Knowledge of (aseptic) pharmaceutical production processes
•    Experience in working with Quality Systems / GMP and experience in working with production control systems would be an advantage
•    Act and behave as the liaison between Quality and Manufacturing departments.
•    Good communication and consulting skills
•    Fluent English knowledge
•    Dutch language knowledge would be an advantage
•    Strong analytical, reporting and planning skills
•    Resistant to a hectic production environment
•    Training and knowledge transfer skills

Function

Investigation and Improvement

Reports to

Head of Investigations & Improvement

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.

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.

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