Manufacturing Process Evaluation Specialist

Grifols Shared Services North America, Inc; Parets del Vallès; Presencial; EUR 42.000 - 63.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Permanent contract

Descripción de la vacante

Grifols Shared Services North America, Inc is hiring a Manufacturing Process Evaluation Specialist in Parets del Vallès to support quality assurance in manufacturing. You will monitor incidents, lead corrective actions, analyze process data, and prepare review reports for audits and inspections.

The role requires a Health Sciences degree (pharmacy/biology/chemistry), GMP knowledge, statistics, English fluency, and 2+ years in quality. We offer a permanent contract in a global healthcare group.

Formación

• You have a Health Sciences Degree (Pharmacy, Biology, Chemistry) and may hold a Master or postgraduate in pharma.
• You know GMP and basic statistics and are proficient with MS Office and SAP.
• You have advanced English and at least 2 years in a similar quality role.

Responsabilidades

• Control and document incidents in production and control processes.
• Supervise corrective or preventive actions from incidents.
• Analyze data and trends from processes.
• Prepare system review reports from analyzed data.
• Coordinate follow-up groups for communication of evaluations and trends.
• Review production operation documentation and equipment/facilities.
• Review qualification and validation protocols and reports.
• Prepare and deliver audit/inspection documentation.

Conocimientos

GMP knowledge

Basic statistics

Advanced English

QA experience

MS Office

SAP

Educación

Health Sciences Degree

Master or postgraduate in pharmaceutical sector

Herramientas

MS Office

SAP

Descripción del empleo

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

We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

We are looking for Manufacturing Process Evaluation Specialist within the Product Quality area of the Quality Assurance division of Instituto Grifols SA, a company specialized in the research, development and production of purified plasma proteins with therapeutic properties obtained from the fractionation of human plasma.

What your responsibilities will be

• You will control and document incidents arising in production and control processes.
• You will supervise the follow-up of corrective or preventive actions derived from incidents in production and control processes.
• You will analyze data and trends from the processes.
• You will prepare system review reports based on the collected and analyzed data.
• You will coordinate follow-up groups to communicate process evaluations and trends.
• You will review documentation that describes production operations and the functioning of equipment and facilities.
• You will review qualification and validation protocols and reports.
• You will prepare and deliver the documentation requested during audits and inspections conducted by national and international organizations and other companies.

Who you are

To perform this job successfully, an individual must be able to perform each essential duty 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).

• You have a minimum education in Health Sciences Degree (Pharmacy, Biology, Chemistry), being valuable to have a Master or Postgraduate degree in the pharmaceutical sector.
• You have knowledge in GMP.
• You have knowledge in Basic Statistics.
• You have knowledge of MS Office and SAP program.
• You have advanced level of English.
• You have at least 2 years of experience in similar position within Quality.

What we offer

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Information about Grifols is available at www.grifols.com.

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Flexibility for U Program: Occasionally remote

Schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits package

• Contract of Employment: Permanent position
• Location: Parets del Vallès

www.grifols.com

Learn more about Grifols