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.

Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Analytical Development Technician like you.

Role Mission

Will be responsible for the analytical development of methods and analytical validations, as well as analytical support during the galenic development and scaling of industrial processes for parenteral solutions and medical devices for the assigned projects.

What your responsibilities will be

• You will define, plan, coordinate, and control the assigned analytical stages or projects together with the department head.

• You will define specifications, procedures, validations, and the analytical strategy to be followed in the project.

• You will generate detailed work plans for the analysts in conjunction with the department head.

• You will define the resources and materials needed to carry out the planning.

• You will manage deviations, analytical investigations, and risk analyses. You will make operational decisions with the help of other departments and the department head.

• You will coordinate and control the execution of planning, activities, resources, departments, and analyses.

• You will design the experimental studies necessary for the analytical development of active ingredients, excipients, intermediates, pharmaceutical specialties, and medical devices.

• You will conduct the theoretical and bibliographical study corresponding to the analytical methodologies for each project.

• You will develop and implement new analytical procedures for active ingredients, packaging, excipients, and finished products.

• You will supervise the physical and chemical analyses of active ingredients, intermediates, medicines, medical devices, packaging, and materials.

• You will maintain and review primary data and laboratory notebooks.

• You will develop and review analytical methods, protocols, and analytical validations, accepting responsibility for them.

• You will oversee the specifications associated with a project, as well as review any analytical documentation to be included in a record.

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).

• Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering.

• You have a Master's degree in the Pharmaceutical Industry or something related to the position. (Desirable).

• Fluent written and spoken English (C1 Advanced) and Spanish.

• You have 3 years of experience in analytical development and method validation, which is highly valued in parenteral dosage forms and in the FDA environment.

• You have 2 years of experience managing work teams.

• You have knowledge of common laboratory techniques (HPLC, GC, UV, KF, IR), of international EMA, FDA and ICH guidelines for drug development and of pharmacopoeias (Ph. Eur. and USP).

• You have knowledge of Empower and Tiamo software, as well as statistical analysis tools such as Minitab. (Desirable).

• You have a good command of the Office suite and SAP (desirable).

• You are a dynamic and proactive person, with a sense of responsibility, organized and methodical, who likes to work in a team.

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!

Grifols is an equal opportunity employer.

Flexibility for U Program: Occasionally Remote

Flexible 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: Parest del Vallès

www.grifols.com

Req ID: 528390

Type: Indefinido tiempo completo

Job Category: I + D