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Senior Project Manager

CHEMO pharmaceutical group

Madrid

Presencial

EUR 45.000 - 60.000

Jornada completa

Hace 7 días

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Descripción de la vacante

La empresa CHEMO pharmaceutical group busca un Project Manager motivado para unirse a su equipo en Madrid. El candidato ideal será responsable de gestionar proyectos complejos en la industria farmacéutica, y necesitará habilidades en comunicación y proactividad, así como experiencia previa en biotecnología. Esta es una gran oportunidad para formar parte de un grupo innovador y en crecimiento.

Servicios

Planes de desarrollo y movilidad interna

Club de beneficios y ahorros

Formación

Más de 5 años de experiencia en una posición similar.
Certificación PMP será un plus.
Fluidez en español e inglés.

Responsabilidades

Asistir en la gestión y ejecución de proyectos de desarrollo y comercialización.
Coordinar equipos multifuncionales para cumplir objetivos de proyecto.
Monitorear el progreso del proyecto y gestionar presupuestos.

Conocimientos

Comunicación

Proactividad

Gestión de riesgos

Educación

Grado en Ciencias de la Vida o campo relacionado

Máster (deseable)

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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. 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 and APIs.

The challenge!

Assist in the management and execution of projects related to the development and commercialization of those APIs and/or drug products.
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.

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): +5 years of experience in a similar position.
Specific Knowledge: understanding of the biotchnology process, 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.
Flexible start time from Monday to Friday (full-time 40 hours).
Benefits and Savings Club.
Development plans, internal mobility policy.

What will the Selection process be like? ️

️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels.

️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test.

️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process.

Do you think this offer is not for you?

Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting!

COMMITMENT TO EQUAL OPPORTUNITIES

The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Seniority level

Seniority level
Associate

Employment type

Employment type
Full-time

Job function

Job function
Project Management
Industries
Pharmaceutical Manufacturing

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