Validation Specialist At Gepd 526047
Validation Specialist At Gepd 526047
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Job Description
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 wellbeing of people around the world. We are leaders in plasmaderived 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 opportunity fostering an inclusive environment where diversity makes us be outstanding.
Help us lead one of the worlds largest pharmaceutical companies. We are a world leader in plasmaderived medicines with a presence in more than 100 countries and a growing global team of over 20.000 people. Thats why we need a Validation Specialist GEPD like you.
Role Mission
Ensure that validations are executed in GEPD with Grifols standards and within the established timeframes
What your responsibilities will be
- Support the new GEDP validation team in managing work teams.
- Prepare documentation (VMP SOP validation reports).
- Provide support for the of validations to ensure they are carried out properly and on schedule.
- Ensures manufacturing cleaning and sterilization validations.
- Develops validation protocols (IQ OQ PQ) and final reports.
- Evaluates deviations and proposes corrective and preventive actions (CAPAs).
- Ensure the qualification of production equipment laboratories and critical services.
- Review and approve suppliers technical documentation.
- Ensure compliance with international regulations (FDA EMA ISO ICH PIC/S).
- Keep documentation and procedures uptodate with GEPD regulatory changes.
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).
- Bachelors degree in Biochemistry Biotechnology Biomedical Engineering Health Sciences or related fields.
- Masters degree in the field of science (Biotechnology Biology Biochemistry Chemistry... (Desirable).
- Excellent verbal and written communication skills in the English and Arab language C1.
- Availability to travel frequently.
- Minimum 1 year of experience in validation areas production procedures within the pharmaceutical sector.
- You have userlevel skills in MS Office
- Knowledge of GMP environment is essential.
- You are proactive methodical and eager to learn
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 . If you are interested in joining our company and you have what it takes for such an exciting position then dont hesitate to apply!
We look forward to receiving your application!
Grifols is an equal opportunity employer.
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active nonexpired Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants in a manner consistent with the requirements of applicable state and local laws.
Schedule: MondayThursday 710 to 1619h and Friday 815h
Benefits package.
Professional Group: 6
Contract of Employment:Permanent position
Location: Parets del Valls
Required Experience:
Unclear Seniority
Employment Type
Full-Time
