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QC Project Manager

On-site in Parets del Vallès·Added 2 days ago (last checked 6 Nov)

Grifols

92 open roles

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Our summary

Work mode: On-site, Parets del Vallès
English: Required
Experience: 2+ years
Education: University degree

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This job advert was originally written in Spanish.

Requirements

What we're looking for

To successfully perform this job, a person must be able to carry out the responsibilities satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

University Degree (Second Cycle) / Bachelor's Degree / Higher Engineering.
2 to 5 years of proven experience.
You have an Advanced level of English.
You have analytical skills.
You have leadership skills and a results orientation.

Pay & benefits

What you'll get

Being part of Grifols means the opportunity to work in an international environment where equal opportunities are promoted.

It means the opportunity to develop professionally, have continuous training, and integrate into a team of professionals where each individual's contribution counts. Our commitment is to maintain an environment that fosters the professional development of our employees in a good work atmosphere.

Grifols' human capital is key to both the development of activities and the company's expansion process.

We believe in diverse talent and want to eliminate any barrier that may prevent your participation. If you need any adjustment in our selection process, please do not hesitate to inform us when applying. We are here to help you.

Flexible schedule: Monday-Thursday 7-10 AM to 4-7 PM and Friday 8 AM-3 PM, with the same flexibility for arrival.

Benefits Package.

Employment contract: Permanent

The role

Would you like to join an international team working to improve the future of the healthcare sector? Do you want to contribute to improving the lives of millions of people? Grifols is a global healthcare company that since 1909 has been improving the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and we develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Help us lead one of the largest pharmaceutical companies in the world. We are a global leader in plasma-derived medicines with a presence in more than 100 countries and a growing global team of more than 20,000 people. That is why we need a QC Project Manager like you.

What you'll do

For the Biopharma division, specialized in the research, development, and production of purified plasma proteins with therapeutic properties obtained from human plasma fractionation, reporting to the Quality Control division, you will be responsible for leading, coordinating, and executing strategic and operational projects within the scope of the division.

You will implement processes, equipment, systems, operational improvements, etc.,
acting as a technical and organizational point of reference.
You will define the necessary procedures and promote their continuous improvement.
You will propose the acquisition of equipment and materials for continuous
development and improvement.
You will collaborate with multidisciplinary teams (QC labs, QA, Engineering, IT,
Regulatory, etc.) ensuring alignment and achievement of objectives.

Execute the various phases of the project, from definition to closure.

You will prepare technical and organizational information.
You will prepare associated documentation (protocols, reports, validation
plans, CAPAs, regulatory justifications, etc.)
You will monitor milestones, deadlines, and deliverables.
You will report the project status to management and stakeholders, preparing the
necessary documentation for decision-making.

Prepare the necessary documentation oriented towards regulatory and other types of requirements

You will develop procedures within the QC scope and advise on the management and
resolution of related incidents.
You will evaluate and propose actions related to regulatory and
other types of changes.
You will propose and carry out the necessary studies and evaluation reports.

How you'll work

Location: Parets del Vallès

Hiring process

4 steps2 interviews

Job search
Start your search on the Grifols careers site or join the Talent Community to stay up to date with the latest jobs posted.
Application
Screening call
With recruitment team · Phone call
If you are shortlisted, the team contacts you for a short screening call about your motivation, skills and experience, and to go into the key details of the role.
Interviews
30–45 min
There are usually two or more interviews of 30 to 45 minutes each; your interviewer will assess your skills and aptitudes with questions focused on the role and your experience.
Decision and offer
Pre-onboarding
Once you accept the offer, the pre-onboarding process begins, with all the information and resources you need for a smooth transition to your new role.

Three people support you: a talent acquisition lead, a hiring manager and an HR manager.

About Grifols

Grifols is a global healthcare company headquartered in Barcelona, Spain, specializing in the development and production of plasma-derived medicines, transfusion medicine, and diagnostic solutions. With operations in over 100 countries and a workforce of more than 20,000 employees, it is one of the world's leading producers of plasma-based therapies, treating chronic and rare diseases. The company operates a vast network of plasma donation centers and manufacturing facilities, making it a key player in the biopharmaceutical industry.

In Spain, Grifols maintains its global headquarters in Barcelona and operates major production and R&D sites in the Catalonia region, including facilities in Parets del Vallès and Sant Cugat del Vallès. The company is deeply rooted in Spain, offering a wide range of roles from laboratory and manufacturing positions to IT, engineering, and corporate functions. For international professionals, Grifols provides a multicultural work environment, opportunities in a highly regulated and innovative sector, and the chance to work in a company that is a global leader in its niche, with Spanish as a common working language alongside English.

Industry: Pharma
Founded: 1909
Employees: 20,000–25,000
Headquarters: Barcelona, Spain
In Spain: Barcelona, Parets del Solès, Sant Cugat del Vallès

Good to know if you are moving

Grifols is headquartered in Barcelona, Spain, and is one of the largest companies in the Catalan region, offering a strong local presence and career opportunities.
The company operates in a highly regulated and innovative sector, providing roles in R&D, manufacturing, and IT, which can be attractive for professionals with experience in biotech or pharma.
While Spanish is the primary language in many roles, the company's global nature means English is often used, especially in IT, corporate, and international positions.
Grifols has a strong commitment to employee development, with trainee programs and continuous learning opportunities, as seen in the STEM Trainee Program IT QA.
The company's global footprint includes operations in the US, Europe, and Asia, offering potential for international mobility within the organization.

In their own words

About the company & team

We believe that diversity adds value to our business, our teams and our culture. We are committed to equal opportunities and our mission is to provide an inclusive environment where differences add to our company.