Quality Program Manager

Job title:

Quality Program Manager

Company:

Nemera

Job description

Company DescriptionWith sales of €500m and 2,800 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing.Nemera’s manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon).We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities.Job DescriptionWould you like to give meaning to your professional career and take part in a project that brings you closer to the patient?Would you like to contribute your skills to a technical and strategic project on an international scale?Nemera has just signed an exciting new contract with one of the world’s leading pharmaceutical groups to industrialize new medical devices at its plant in Poland. The project is just getting underway! Get on the first train! Come and join us!The Senior Quality Project Manager is responsible for ensuring that:New projects and life cycle of existing products are properly managed as per NPI, de-risked, documented and transferred to production.Control plan for new projects / products are properly defined to achieve compliance with customers or Insight specifications.What You’ll Do:

• Manages the Quality Project Engineers for the new projects/products and for the life cycle management of these products.
• Maintains manufacturing equipment in a validated status (change control, periodic review)
• Manages all the quality topics related to projects / new products under industrialization.
• Provides guidance and support to project teams, facilitating problem solving, and decision making to ensure that expected quality level is achieved.
• Ensures control plan for new projects / products are properly defined to achieve compliance with customers or Insight specifications.
• Ensures transfer of quality project outputs to operational quality, QC and production
• Ensures NPI is properly applied and documented by the projects teams.

QualificationsPosition requirements:

• Engineer degree
• Experience in pharma or medical device industry

Preferred Knowledge/skills

• Knowledge of injection molding.
• Knowledge of ISO 13485 and ISO 14971 (risk management)
• Knowledge of pharmaceutical cGMPs and pharma validation.
• Knowledge of project management.
• Knowledge of problem-solving tools (QRQC, 5Whys, Ishikawa, DOEs)
• Fluent in English.
• Recognizes individual and collective efforts.
• Delegates actions and decisions.
• Promotes standard processes, roles and responsibilities.
• Deals constructively with complex problems.
• Executes the strategy.
• Prioritizes activities and resources.
• Inspires and is pragmatic.
• Grants individuals’ development goals
• Manages as a coach.

Additional InformationWe believe in a transparent and straightforward recruitment process to ensure a great fit for both you and our team.Here’s what you can expect:

• CV Review: Upon receiving your CV, our Talent Acquisition Team will review it to assess your qualifications for the role.
• Initial Screening: If your profile matches our requirements, you’ll be invited for an initial screening call with a member of our Talent Acquisition Team.
• Interview with Hiring Manager: After the initial screening, you’ll have an interview with the Hiring Manager to discuss your experience, skills, and fit for the role in more detail.
• Interview with N+2: Following the Hiring Manager interview, you’ll meet with the next level of management (N+2) for further evaluation.
• HR Manager Interview: The final step involves an interview with our HR Manager to discuss company culture, benefits, and other HR-related topics.
• Offer: If all goes well, you’ll receive an offer to join our team!

We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group, if you want to discover more about Nemera, please look at our website www.nemera.netKnow someone at Nemera? We have a Referral Program so, be sure to have them submit you as a referral prior to applying for this position!Nemera to światowy lider w dziedzinie projektowania, rozwijania i produkcji urządzeń do podawania leków dla przemysłu farmaceutycznego, biotechnologicznego i generycznego.
Posiadamy lokalizacje na całym świecie a nasze usługi i produkty obejmują kroplomierze, pompy, zawory, inhalatory, dozowniki bezpowietrzne i autostrzykawki.Podczas tworzenia urządzeń do podawania leków stawiamy pacjentów na pierwszym miejscu, ponieważ wiemy, że dokładne dawkowanie leków i ergonomia przyczyniają się do szybszego zakończenia leczenia.
Praca w Nemera oznacza bycie częścią zespołu, który naprawdę cieszy się wspólną pracą i zawsze idzie o krok dalej, aby wypełnić swoje zobowiązania. Jesteśmy dumni z pracy, którą wykonujemy, ponieważ poprawia ona życie pacjentów.W Nemera cenimy różnorodność i inkluzywność.
Jesteśmy dumni, że jesteśmy pracodawcą równych szans i zachęcamy do składania aplikacji przez osoby z różnych środowisk, płci, orientacji seksualnych oraz grup wiekowych.

Expected salary

Location

Szczecin, zachodniopomorskie

Job date

Thu, 02 May 2024 22:30:26 GMT

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