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Senior Project Manager – Generic Drug Development

Chemo

Madrid

Presencial

EUR 60.000 - 80.000

Jornada completa

Ayer
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Descripción de la vacante

A global pharmaceutical company in Madrid is seeking a Senior Project Manager with over 5 years of relevant pharmaceutical experience. This role requires fluent Spanish and English, along with strong project management skills to oversee complex drug development and commercialization projects. The ideal candidate will coordinate cross-functional teams and ensure adherence to timelines and budgets while actively managing risks. The company offers a permanent contract with a flexible schedule and an attractive salary package.

Servicios

Flexible start time
Permanent contract
Attractive salary package

Formación

  • Mandatory +5 years of experience in a similar position in the pharma industry.
  • PMP Certification will be an asset.
  • Understanding of the drug development process and regulatory requirements.

Responsabilidades

  • Manage and execute projects related to the development and commercialization of generic drugs.
  • Coordinate cross-functional teams to ensure project timelines and budgets are met.
  • Monitor project progress and identify potential risks.

Conocimientos

Project management
Fluent Spanish
Fluent English
Communication skills
Risk management
Customer focus

Educación

University Degree in Life Science
Master's Degree
Descripción del empleo
In a few words

Position: Senior Project Manager

Location: Madrid

Experience: +5 years in Pharma Industry

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 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development.

Ready to be a #Challenger?
What are we looking for?

We are seeking a motivated and client‑oriented Senior Project Manager to join our growing team in the pharmaceutical industry. The candidate will manage moderately large or complex projects that require proven project management skills. Role will be involved in the planning, coordination, and execution of projects related to the development of drug products mainly but not only generic pharmaceuticals.

The challenge!
  • Assist in the management and execution of projects related to the development and commercialization of generic drugs.
  • Understand the needs of the internal and external customers, projects and align them with the strategic guidelines of Chemo.
  • Coordinate cross‑functional teams, including but not limited to R&D, regulatory affairs, clinical department, manufacturing, patents, sales to ensure project timelines, budgets, product costing and objectives are met.
  • Analyze the characteristics and needs of each project, evaluating processes end to end.
  • Support the creation and maintenance of project schedules, timelines, cost evaluation and relevant project documentation. Planning the milestones of a project and identify the milestone owners.
  • Assist in preparing project reports, presentations, and updates for senior management and stakeholders.
  • Participate in meetings with internal, external partners, vendors among others as needed.
  • Communicate properly and in time with clients and/or partners.
  • Monitor project progress and identify potential risks, issues, or delays and work collaboratively in mitigation plans by providing alternatives or contingency plans.
  • Track and manage project budgets and identify possible deviations.
  • Establish / develop and maintain systems and communication and control processes (registration system and information about project progress, deviations, actions) CRM, BI, etc.
  • Revise project plans, status and budget for short‑term and mid‑term business plans.
  • Report management about deviations of approved assumptions of projects.
  • Revise project sales expectations, NPV and business cases on regular basis.
What do you need?
  • Education: University Degree in Life Science or related field. Master is a plus.
  • Languages: Fluent Spanish and English, knowledge of other languages will be an asset.
  • Experience (years/area): mandatory +5 years of experience in a similar position in pharma industry.
  • Specific Knowledge: Understanding of the drug development process, regulatory requirements. PMP Certification will be an asset.
  • Travels: Open to travel worldwide.
  • Personal skills: impact and influence, ability to maintain a positive work environment, strong verbal and written communication skills, proactive in identifying risk and ability to manage challenges and adapt to changes, sensitivity to market evolution, ability to handle competing priorities, good interpersonal skills, result orientation, customer focus.
Our benefits!
  1. ⏰ Flexible start time from Monday to Friday (full‑time 40 hours).
  2. Permanent contract.
  3. Attractive salary package.
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