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Senior project manager

Ourense
Chemo
Publicada el 6 septiembre
Descripción

In a few words

Position :
Senior Project Manager

Location :
Madrid

Experience :
+5 years

Want to know more?

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health.

The activities of INSUD PHARMA are organized into three synergistic business areas:
Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA emphasizes innovation and sustainable development.

Ready to be a #Challenger?

What are we looking for?

We seek a motivated, client-oriented Project Manager to join our growing team in the pharmaceutical industry. The candidate will manage moderately large or complex projects requiring proven project management skills. Experience in biotechnology, fermentation processes, and upstream/downstream operations is preferable. The role involves planning, coordination, and execution of projects related to drug product development, mainly but not only for generic pharmaceuticals and APIs.

The challenge!

* Assist in managing and executing projects related to the development and commercialization of APIs and drug products.
* Understand and align internal and external customer needs with Chemo's strategic guidelines.
* Coordinate cross-functional teams including R&D, regulatory affairs, clinical, manufacturing, patents, and sales to ensure project timelines, budgets, and objectives are met.
* Analyze project characteristics, evaluate processes end-to-end, and support the creation and maintenance of project schedules, timelines, and documentation. Plan milestones and assign owners.
* Prepare project reports, presentations, and updates for senior management and stakeholders.
* Participate in meetings with internal and external partners, vendors, and others as needed.

Ensure proper and timely communication with clients and partners.

* Monitor project progress, identify risks, issues, or delays, and collaborate on mitigation and contingency plans.
* Track and manage project budgets, addressing deviations.
* Establish and maintain systems for communication and control, such as registration systems and project tracking tools like CRM and BI.
* Review project plans, status, and budgets for short- and mid-term business planning.

What do you need?

* University Degree in Life Sciences or related field;
a Master’s degree is a plus.
* Fluent in Spanish and English;
knowledge of additionallanguages is an asset.
* Over 5 years of experience in a similar role.
* Knowledge of biotechnology processes, drug development, and regulatory requirements;
PMP certification is anasset.
* Willing to travel worldwide.
* Personal skills include impact and influence, positive work environment, strong communication, proactive risk management, market sensitivity, ability to handle priorities, interpersonal skills, result orientation, and customer focus.

Our benefits!

* Flexible start time, Monday to Friday (full-time 40 hours).
* Permanent contract.
* Attractive salary package.
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