Principal Scientist Salary at Pepgen Inc BETA

Principal Associate Scientist Location: Cambridge, Massachusetts (On Site) Job Description: Responsibilities: The Principal Associate Scientist will be responsible for non-GMP analytical testing using non-chromatographic [stand-alone UV assay, pH, Osmolality, moisture, thermal melting temperature determination using UV] and chromatographic [reverse phase, ion exchange] methods. The candidate will also be responsible for reporting analytical data generated in appropriate electronic notebooks; the responsibilities also include writing/reviewing protocols, reports, certificates of testing and other relevant documents. Additional responsibilities include data mining and compiling historical/relevant information. Appropriate training will be provided for oligonucleotide specific techniques; however, expertise of core instrumentation/skill set in analytical chemistry is required. Summary of Key Responsibilities: • Perform in-house non-GMP analytical testing using non-chromatographic [stand-a

Job Description Join the Alkermes Formulation Development team as a Principal Scientist, where you will lead the development of innovative small molecule pharmaceutical dosage forms. You will provide strategic and technical direction for drug product development and play a major role in the CMC and development teams. You will design and execute experiments with a focus on product understanding and robustness, interpret data, and write technical and regulatory documents. Responsibilities Provide technical leadership in designing and executing lab-based experiments to develop small molecule immediate or modified release formulations across various stages, from concept to commercialization. Give strategic planning to meet project deliverables within timelines, incorporating both immediate and long-term goals. Integrate Quality Risk Management (QRM) and Quality by Design (QbD) principles into project activities. Collaborate within cross-functional teams to execute development strategies th

Job Description The Principal Scientist position within Analytical Development provides technical leadership for small molecule analytical methodologies and grows as a subject matter expert both within and outside the department as part of a growing, dynamic Pharmaceutical Development organization. They will work within the Analytical Development team to characterize drug substance, drug product, impurities, degradants, and metabolites from pre-clinical research through drug development and commercialization. The successful candidate will thrive in a highly collaborative matrix team environment to drive critical decision-making and ensure the successful development of new drugs. Responsibilities Responsibilities: Provide subject matter expertise in analytical development methodologies at Alkermes requiring internal laboratory execution and technical oversight/supervision Guide and drive analytical method development, method implementation, product characterization and analytical contro

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Analytical Quality Control program manager and primary planner of internal and external products ranging from new product introductions through commercialization. Assess and drive method changes, analytical improvements and provides technical support to cross-functional teams within and outside of QC during all stages of product development. Accountable for validation, method transfers, data analysis of study results, chromatographic overlays and t

Industry: Pharmaceuticals Title: Principal Associate Scientist Job ID: 2025-9073 Location: Cambridge, MA Duration: 10 months contract (+Chances of extension) Responsibilities: The Principal Associate Scientist will be responsible for non-GMP analytical testing using non-chromatographic [stand-alone UV assay, pH, Osmolality, moisture, thermal melting temperature determination using UV] and chromatographic [reverse phase, ion exchange] methods. The candidate will also be responsible for reporting analytical data generated in appropriate electronic notebooks; the responsibilities also include writing/reviewing protocols, reports, certificates of testing and other relevant documents. Additional responsibilities include data mining and compiling historical/relevant information. Appropriate training will be provided for oligonucleotide specific techniques; however, expertise of core instrumentation/skill set in analytical chemistry is required. Summary of Key Responsibilities: Perform in-hou

About the job Principal Scientist, DMPK Job Title: Principal Scientist, DMPK Job Location: Boston, MA, USA Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Mid-Senior level The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Our Endosomal Escape Vehicle (EEV™)-therapeutics are designed to enable the efficient intracellular delivery of a wide range of therapeutics into a variety of organs and tissues, resulting in an improved therapeutic index. Through this proprietary, versatile and modular approach, Entrada is advancing a robust development portfolio of RNA-, antibody- and enzyme-based programs for the potential treatment of neuromuscular, ocular, metabolic and immunological diseases, among others. Our lead oligonucleotide programs are in

Job Type Full-time Description About the Opportunity Meadowhawk Biolabs is seeking an enthusiastic and highly motivated Scientist to work within the non-GLP Immunoanalytical Services Team at our Marlborough, MA site. The ideal candidate is creative, hardworking, results focused, driven and has prior experience in Cell based assays and Flow Cytometry for analysis of biologically derived samples. Given that we are a newly launched Contract Research Organization (CRO) founded by an experienced team of industry veterans, this position offers unique ground floor opportunities for the successful candidate to contribute meaningfully to the creation and development of our services, expand their knowledge base by participation in multidisciplinary teams, and advance their career in capabilities and responsibilities. Key Roles and Responsibilities: •Independently conduct quantitative flow cytometry methods of varying complexity to study both cell-surface and intracellular targets •Critically rev

Company Overview: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE™ platform, Dyne is developing targeted therapeutics that deliver to muscle and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. For more information, please visit https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook. Role Summary: Dyne is seeking a Principal Scientist in protein engineering to drive new therapeutic molecules for rare genetic diseases. Responsibilities include designing, discovering, and producing candidate molecules, such as antibodies and fusion proteins. The candidate will support and lead drug discovery projects,