Process Development Scientist Salary at Landmark Bio BETA

A Third Rock Ventures Stealth NewCo is seeking a Formulations Scientist/ Senior Scientist and Drug Product Lead who is interested in establishing core operations of a new team. This position will be a laboratory-based role and will offer tremendous opportunities to advance programs, develop new workflows, implement devices, and build a laboratory. Successful candidates will be innovative, thrive in a startup environment and use their creative and imaginative problem-solving skills to help bring new products to patients. RESPONBILITIES Work collaboratively with discovery, non-clinical, clinical, and CMC teams to develop and deliver phase-appropriate materials for animal and clinical studies. Develop robust formulations for novel protein therapeutics and dosage forms for early/late-stage development. Establish an internal formulation development laboratory with analytical capabilities and execute studies (formulations screening, DP in-use/compatibility, etc.) for drug candidates. Manage

ODDITY Labs is hiring for a Topical Delivery specialist to develop a best-in-class playbook for optimizing the penetration of our topically applied therapeutics. Specific responsibilities Develop a playbook for maximizing topical delivery that taps into the strongest existing research in skin penetration, but is customized to our use case Own the hands on execution of the playbook, with support from an existing team of chemists & formulators Develop and maintain rigorous standards for testing and optimizing deliverability Commission or conduct cutting edge research into new topical delivery modalities for our applications Maintain a network of experts in the topical delivery space to ensure we are always appraised of the newest developments in the space Keep finger on the pulse of innovations in topical delivery to ensure we are always implementing the most cutting edge technologies Qualifications 7-10 years of experience in Topical Delivery, with at least 5 years in Industry. Ideally

Associate Scientist II, Genomic Medicine (AAV) Drug Location: Cambridge, MA Duration: ____12 months _______ Execution of formulation studies and non-GMP stability studies for AAV-based drug candidates. Clinical administrative device compatibility and In-use studies for clinical dosing enablement. Supporting the development of GMP fill finish processes. Developing presentations for internal presentations. Technical report authoring and data verification. Required Skills BS in Pharmaceutics, Biochemistry, Chemical Engineering, or relevant field with 2+ years, a MS with 1+ years of relevant experience. Hands on experience with biologic drug development. Understanding of protein chemistry, formulation, and degradation. Ability to work effectively in a cross-functional settings. Excellent interpersonal and communication skills. Preferred Skills Experience developing stabilizing, clinically acceptable formulations, and fill finish processes for biologics. Experience with biopharmaceutical as

Job Description Job Description Job Title: Part-Time Materials Scientist with Expertise in Polymer Chemistry Job Description: We are seeking a highly qualified and motivated individual with advanced education and training in Materials Science and Polymer Chemistry for a part-time/flex hours position. The successful candidate will play a key role in developing and characterizing cutting-edge polymer materials enhanced with metallic additives, using a proprietary loading methodology. Key Responsibilities: Polymer Loading: Perform precise loading of polymers with metallic additives using proprietary methodologies. Characterization & Testing: Verify chemical compositions of loaded polymer batches using advanced laboratory instrumentation such as X-ray Photoelectron Spectroscopy (XPS) or equivalent analytical tools. Sample Preparation: Prepare polymer batches for testing and evaluation by corporate partners. Lab Equipment Expertise: Utilize and maintain advanced laboratory equipment, includ

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Downstream Process Development Scientist for Cytiva is responsible for supporting the Fast Trak Process Development Services (PDS) group by prov

Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Senior Downstream Process Development Scientist for Cytiva is responsible for accelerating discovery, development and delivery of solutions that

Key Responsibilities: Design and implement robust computational and statistical methods to analyze large scale proteomics and metabolomics datasets. Develop automated data processing pipelines in collaboration with our cloud infrastructure team. Establish tools for the analysis, visualization, and reporting data in collaboration with scientists and other stakeholders. Collaborate closely with our chemoproteomics, synthetic biology, and metabolomics teams to identify and build enabling solutions. Integrate in-house datasets with public resources (GNPS, BioPlex, DepMap, etc.) to better understand disease biology and drive drug discovery programs. Qualifications: Ph.D. with 1+ years or M.S. with 3+ years of relevant data science and software development experience High level of proficiency in programming languages such as Python and/or R. Experience working with biological and mass spectrometry data types including chemoproteomics, proteomics, metabolomics, and natural product structures

"We are focused on results. Those that can be measured. And those measured in ways beyond numbers. We see individuals, not issues. We are inspired by passion, and compassion for the wellbeing of people. Our methods are based on logic, driven by rigor, results, issues, and outcomes. Our innovation means trying new things, learning from our mistakes, and consistently refining our approach. Our strategies help us define our path to success, but our effectiveness is based in the aggregate power of our initiatives to impact holistic change." -Bill Gates and Melinda French-Gates The Bill & Melinda Gates Medical Research Institute (Gates MRI) is a non-profit biopharmaceutical development organization primarily dedicated to the development of impactful biopharmaceutical interventions for diseases that disproportionately affect the world's poorest populations, diseases that combined cause five deaths every minute. Headquartered in Cambridge MA, the Institute is designed to advance novel drug, b