Company description: At Pfizer, our purpose is to deliver breakthroughs that change patients lives. As a Senior Associate Scientist, you will be at the forefront of this mission, working within our Research & Development division. Your role will be pivotal in translating advanced science and technologies into therapies and vaccines that matter most. By leveraging cutting-edge design and process development capabilities, you will help accelerate the delivery of best-in-class medicines to patients globally, ultimately improving their lives. What You Will Achieve As a Senior Associate Scientist in Analytical Research and Development, you will take an active role in supporting drug development by applying a variety of analytical methodologies to support physical and chemical characterization of drug substances (including raw materials and intermediates). Working knowledge and ability to operate analytical techniques such as chromatography and spectroscopy used for the characterization of pharmaceutical substances and products is desired. Job description: Perform laboratory work in support of analytical testing of pharmaceutical projects with using but not limited to the following analytical methodologies: chromatography, KF, spectroscopy or mass spectrometry. Method development, validation and transfer of analytical methods Responsibilities will include testing and release of raw materials and intermediates to support pharmaceutical development efforts, documentation of experimental results. 24/7 In-process control (IPC) support for plant operations Effectively interact with project team members for various tasks including presentation of data and critical review of data and preparation of technical reports. Demonstrate proficiency with a wide variety of software and information systems. The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team and thrive in a fast-paced environment. Demonstrated attention to detail, strong organizational skills, the ability to multitask and meet project timelines. Assist in the maintenance and renewal of laboratory instruments, systems or apparatus, and in the maintenance and continuous improvement of safe and effective working practices. Independently carry out all aspects of practical work necessary to provide right first time results. Required profile: BSc with a minimum of 2 years relevant experience either in a GMP lab environment, or an academic or industrial research lab. Ability to meet project milestones under general supervision, manage expectations for specific projects, ensure delivery of technology/transfer/submission-ready technology, data and documents. Experience in problem-solving skills and instrument troubleshooting. Demonstrated oral and written communication skills, especially adherence to laboratory notebook practices. Experience with a wide variety of software and information systems (e.g. electronic lab notebooks, Empower/OpenLab and LIMS). Ability to work in a team environment in GMP laboratory environment performing experiments Ability to perform data analysis, record results in electronic lab notebooks and effectively communicate in a team environment. Ability to adhere to safe laboratory practices Good documentation skills with high attention to detail, strong organizational skills, team oriented, effective interpersonal and communication skills. Nice-to-Have (one or more of the following) Experience in the pharmaceutical industry Analytical method development experience Experience working in a regulated environment Experience with chromatography techniques (HPLC, GC, HPLC-MS) Knowledgeable in vibrational spectroscopy (NIR, IR, Raman, UV-Vis) NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Do not anticipate more than 10% travel. Must be open to support shift work when required Skills: Scientist Associate Associate Scientist