Formulation Development Manager
As Formulation Development Manager, you will lead scientific strategy and team performance for advanced drug delivery systems.
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This job advert was originally written in Spanish.
Degree in Chemistry, Pharmaceutical Sciences, Biotechnology, or similar.
At least 2 years of professional experience.
Intermediate English, spoken and written.
Temporary contract for substitution.
Position with a high level of learning and continuous improvement.
Very good working environment.
Flexible hours.
Curapath is a full-service CDMO (Contract Developing and Manufacturing Organizations) that connects innovative technology and scientific precision, centralizing your manufacturing process from preclinical to clinical development. We offer the best drug delivery solutions to potential clients seeking specific therapies.
We believe in science to transform the world, and we want the people who work at Curapath to thrive in an environment that makes this possible. That is why we are committed to developing the talent of every person in our company.
Understand, use, and execute the SOPs and instructions provided, including sampling and analysis of raw materials, stability studies, IPC, release, R&D samples, standards, and cleaning verifications.
Perform routine laboratory work such as mobile phase preparation, equipment conditioning, preparation of standards and samples, measurements, stock controls, and basic equipment maintenance.
Perform basic handling of analytical equipment such as chromatography, IR, Karl Fischer, pH/conductivity, and osmolality.
Prepare samples, execute SOPs, and perform basic calculations and data analysis under guidance.
Draft the investigation part of deviations, change controls, CAPAs, and OOS under supervision.
Prepare certificates of analysis (CoAs) in accordance with established specifications.
Draft SOPs, analytical methods, TIs, general procedures, protocols, and reports following existing templates, as well as maintaining the laboratory notebook.
Use and understand relevant technical bibliography.
Routinely control standards, reagents, and product/solution stocks, ensuring their proper labeling, storage, and traceability.
Participate in the general cleaning of the workplace and in maintaining laboratory order, complying with established good practices.
Curapath is a biotech Contract Development and Manufacturing Organization (CDMO) based in Barcelona, Spain, specializing in the development and production of advanced therapies, including cell and gene therapies. The company provides end-to-end services from process development to clinical and commercial manufacturing, supporting biotech and pharmaceutical clients in bringing innovative treatments to market. As a CDMO, Curapath operates at the intersection of biotechnology and manufacturing, with a focus on quality, regulatory compliance, and scalability.
Curapath's operations are centered in Barcelona, a key European biotech hub, and the company is actively expanding its team to support growing client demand. The work culture emphasizes scientific excellence, innovation, and collaboration, making it an attractive destination for international professionals with expertise in bioprocessing, quality assurance, and regulatory affairs. With a small but growing team, Curapath offers the opportunity to have a significant impact in a fast-paced, mission-driven environment.
At Curapath, we are looking for a Quality Control Technician to join our team. The selected person will execute the necessary actions to ensure the satisfactory completion of the assigned project, guaranteeing overall alignment with Curapath's objectives.
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