Quality Control and R&D Analyst

• Conduct physical and chemical analyses of raw materials, in process controls, final products and stability samples according to established regulations and procedures.
• Carrying out analyzes corresponding to the development of new medicines, analytical transfers and validation of analytical methods.
• Maintain in good condition the equipment and materials used to carry out their tests.
• Guarantee the integrity of the analytical data generated and/or reviewed that applies.
• Write down and register the data of incidents/abnormal results detected.
• Participate in the first phase investigation of OOS/OOE/OOT results that apply in physicochemical area.
• Physicochemical analysis (HPLC, GC, IR, UV spectrophotometry, potentiometry, etc).
• To support management of reagents, laboratory material, performance of various tests, cleaning of the material used, generation of reports, etc.

• CFGS/FP II in Quality Control or Analytics.
• Minimum 2 years of work experience in quality control department under EU-GMP
• HPLC: demonstrable experience of more than 2 years.
• Experience in validation of analytical methods is a plus.
• Technical English for preparing of Certificate of Analysis
• Experience in working under SAP or LIMS software
• Ability to work independently executing the stablished SOPs.
• Flexible mind for work in a multinational, multitask and multiteam environment.
• Open approach to work in shift changes, first period from 8:00-10:00 to 16:00-18:00 and second period could be from 6:00 to 14:00 or from 14:00 to 22:00.

• Deep experience in the opening of a new manufacturing and R&D facility in Spain.
• Opportunity to develop the project from the very beginning.
• Competitive remuneration, according to the proven experience.
• Personal development plan according to the responsibilities and assigned targets

Page Personnel