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 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. Experience in biotechnology, fermentation processes, and upstream/downstream operations is preferable. The role will involve planning, coordination, and execution of projects related to the development of drug products, mainly but not only generic pharmaceuticals and APIs.
The challenge!
* Assist in managing and executing projects related to the development and commercialization of APIs and/or drug products.
* Understand the needs of internal and external customers, projects, and align them with the strategic guidelines of Chemo.
* Coordinate cross-functional teams, including R&D, regulatory affairs, clinical, manufacturing, patents, and sales to ensure project timelines, budgets, product costing, and objectives are met.
* Analyze project characteristics and needs, evaluate processes end-to-end, and support the creation and maintenance of project schedules, timelines, and documentation. Plan milestones and identify owners.
* Assist in preparing project reports, presentations, and updates for senior management and stakeholders.
* Participate in meetings with internal and external partners, vendors, among others.
Communicate effectively and timely with clients and partners.
* Monitor project progress, identify risks, issues, or delays, and work collaboratively on mitigation plans with alternatives or contingency measures.
* Track and manage project budgets, identifying deviations.
* Establish and maintain systems and communication processes (registration systems, project progress info, deviations, actions) using CRM, BI, etc.
* Review project plans, status, and budgets for short- and mid-term business planning.
What do you need?
* Education: University Degree in Life Sciences or related field; Master’s preferred.
* Languages: Fluent Spanish and English; knowledge of additional languages is a plus.
* Experience: +5 years in a similar role.
* Specific Knowledge: Understanding of biotechnology processes, drug development, regulatory requirements; PMP certification is an asset.
* Travel: Willing to travel worldwide.
* Personal Skills: Impact and influence, positive work environment, strong communication skills, proactive risk management, adaptability, market sensitivity, interpersonal skills, result-oriented, customer focus.
* Work Schedule: Flexible start time, Monday to Friday, full-time (40 hours).
* Contract: Permanent.
* Salary: Attractive package.
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