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Senior Project Professional

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 experienced project manager looking for a new challenge in the pharmaceutical industry? Are you motivated by improvement and growth? Then the Investigation and Improvement team is the right fit for you! Join Teva Haarlem as a Senior Project Professional! Be part of this dynamic team, which is the brain of the company! Help us to execute improvement projects within production and work together with various teams to improve our processes. Initiate changes and execute CAPA’s in the Manufacturing department in response to production deviations, audit observations, or as part of continuous improvement. Make recommendations for working conditions ans assess current processes!

Your responsibilities

Responsible for the execution of improvement projects within production, including:

Ensure the execution of improvement project activities related to pharmaceutical manufacturing processes (bulk production and packaging):

•    Drawing up, initiating, and executing CAPA’s and Changes in the Manufacturing department in response to production deviations, (internal and external) audit observations, or as part of continuous improvement.
•    Executing updates of SOP’s and implementation of new working procedures and technical improvements. The projects may relate to Safety, Quality or Operational excellence.
•    Performing Impact Assessments related to Changes.
•    Writing test protocols and reports related to the CAPA’s and Changes.
•    Representing the production department and providing production knowledge in project teams for introduction of Capex.

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

•    Assess current processes and write justifications or initiate changes where applicable.
•    Making recommendations for working conditions, (product) safety and the environment.
•    Support the production department in case of safety, process, or quality issues.
•    Make proposals to improve manufacturing methods and to implement developments in manufacturing technology.
•    Participate in various projects to improve quality aspects.

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

•    Reviewing SOPs.
•    Support with Compliance investigations and Audit responses.
•    Knowledge transfer, training of manufacturing personnel or technicians.

Your profile

•    Minimum of a bachelor degree in Pharmacy, Pharmaceutical technology, Bio-Chemistry or any technical field.
•    At least 3 years of work experience in the pharmacautical, chemical, biotechnology or food industry.
•    Knowledge of (aseptic) pharmaceutical production processes.
•    Basic technical knowledge of manufacturing equipment.
•    Experience in working with Quality Systems / GMP.
•    Experience in working with production control systems.
•    Act and behave as the liaison between Quality, Technical 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.
•    Result-driven, team-player attitude.

Function

Project management

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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