Analytical Development Technician

Description

Job Summary: Grifols is seeking an Analytical Development Technician for its R&D area, responsible for the development and validation of analytical methods and supporting projects involving parenteral solutions and healthcare products. Key Highlights: 1. Join an international team improving global health. 2. Be part of a leading company in transfusion medicine and hemoderivatives. 3. Opportunity for professional development in an inclusive environment. Would you like to join an international team working to improve the future of healthcare? Do you want to contribute to improving the lives of millions of people? Grifols is a global healthcare company that has been enhancing people’s health and well-being worldwide since 1909. We are leaders in hemoderivative medicines and transfusion medicine, and we develop, manufacture, and market innovative medicines, solutions, and services in over 110 countries and regions. **We believe 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 strengthen our company.** Within the R\+D area of Grifols S.A. Laboratories, we require an *Analytical Development Technician* who will be responsible for analytical method development and analytical validations, as well as providing analytical support during galenic development and industrial process scale-up of parenteral solutions and healthcare products for assigned projects. **Your responsibilities will include:** * Defining, planning, coordinating, and monitoring assigned analytical stages or projects together with the department head. * Based on the project proposal, defining specifications, procedures, validations, and the analytical strategy to follow. * Developing a detailed work plan for analysts jointly with the department head. * Defining the resources and materials required to implement the plan. * Managing deviations, analytical investigations, and risk analyses. Making operational decisions with support from other departments and the department head. * Coordinating and monitoring execution of the plan, activities, resources, departments, and analyses. * Designing necessary experimental studies for analytical development of active pharmaceutical ingredients (APIs), excipients, intermediates, pharmaceutical specialties, and healthcare products. * Conducting the theoretical and bibliographic study of analytical methodologies for each project. * Reviewing and interpreting results. * Developing and implementing new analytical procedures for APIs, containers, excipients, and finished products. * Supervising physicochemical analyses of APIs, intermediates, medicines, healthcare products, containers, and materials. * Maintaining and reviewing primary data and laboratory notebooks. * Preparing and reviewing technical documentation and area documentation. * Preparing and reviewing analytical methods, protocols, and analytical validations, assuming responsibility for them. * Supervising project-related specifications, as well as reviewing any analytical documentation to be included in a regulatory filing. **Who You Are** To perform this role successfully, a person must be able to satisfactorily carry out the responsibilities listed above. The requirements below are representative of the knowledge, skills, education, and/or abilities required. Role adaptations may be made to enable individuals with functional diversity to perform the job tasks. * You hold a Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related field, and possess a Master’s degree in Pharmaceutical Industry or a closely related discipline. * You preferably bring at least 3 years’ experience in analytical development and method validation, with positive consideration given to experience in parenteral dosage forms and within an FDA-regulated environment. * You possess knowledge of standard laboratory techniques (HPLC, GC, UV, KF, IR), international guidelines (EMA, FDA, ICH) for drug development, and pharmacopoeias (Ph. Eur. and USP). * You have experience with Empower and Tiamo software, as well as statistical analysis tools (e.g., Minitab); such knowledge is considered advantageous. * You are proficient in Microsoft Office applications. * You are familiar with SAP, which is considered advantageous. * You have an advanced level of English (B2.2–C1). * You are dynamic and proactive, responsible, organized, and methodical, and enjoy working collaboratively in a team. **What We Offer** Joining Grifols means having the opportunity to work in an internationally oriented environment that promotes equal opportunities. It means having the opportunity to develop professionally, access continuous training, and become part of a team of professionals where each individual’s contribution matters. Our commitment is to maintain an environment that fosters our employees’ professional development within a positive workplace atmosphere. The human capital of Grifols is key both to carrying out our activities and to the company’s expansion process. We believe in diverse talent and aim to eliminate any barriers that could hinder your participation. If you require any accommodations during our selection process, please do not hesitate to inform us when applying. We are here to help. **Flexible Schedule:** Monday–Thursday: 7–10 a.m. and 4–7 p.m.; Friday: 8 a.m.–3 p.m., with the same flexibility regarding start time.**Benefits Package****Employment Contract:** Permanent**Flexibility for U Program:** Up to 1 remote working day per week**Location:** Parets del Vallès **Location:** **SPAIN : Spain : Parets del Vallès****:****\[\[cust\_building]] Learn more about Grifols