Manufacturing Process Evaluation Specialist at GRIFOLS, S.A.

Parets del Vallès, Catalonia, Spain -

Full Time

Start Date

Immediate

Expiry Date

20 Sep, 26

Salary

0.0

Posted On

22 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP, Basic Statistics, MS Office, SAP, English Proficiency, Quality Assurance, Process Evaluation, Data Analysis, Incident Documentation, Audit Preparation

Industry

Pharmaceutical Manufacturing

Description

table.MiTabla { max-width: 1020px;!important 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 Quality Management 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 production and control protocols for processed batches. 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 Assurance. 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. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! 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 Flexible schedule: Monday-Thursday 8h to 17h and Friday 8-15h. Benefits package Contract of Employment: Permanent position Location: Parets del Vallès www.grifols.com Location: SPAIN : España : Parets del Valles:[[cust_building]] Learn more about Grifols

Responsibilities

The specialist will control and document production incidents, analyze process trends, and prepare system review reports. They are also responsible for reviewing production protocols, validation reports, and providing documentation for audits.