Job Postings

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Associate Scientist/Senior Associate Scientist – iPSC

 

Apply for the Associate Scientist position opening at Casma Therapeutics.


Senior Research Associate/Associate Scientist - iPSC

Apply for the Senior Associate Scientist position opening at Casma Therapeutics.


Associate Director, Regulatory Affairs, Medical Writing

Blueprint Medicines is a global precision therapy company that invents life-changing therapies for people with cancer and hematologic disorders. We are looking to hire for a Associate Director of Regulatory affairs/Medical Writing. The Associate Director (MW) is responsible for clinical strategic document expertise across the global regulatory marketed and development portfolio. This individual will support and guide all clinical regulatory documents to be included in eCTD submissions and other global health authority (HA) submission types, including all original applications, information requests, amendments, responses, and all other clinical submission types. This person will supervise regulatory writing vendors to manage submission documents and ensure the science-supported clinical messaging is clear and concise and is fully aligned with program team strategy. This individual will collaborate with cross functional teams providing timelines and overall medical writing document management activities. The MW will provide regulatory system and authoring template assessments to further develop and enhance the regulatory writing processes, deliver high-quality submission-ready documents to contribute to Blueprint Medicines overall company objectives. More information for the Associate Director.


Senior Manager/Associate Director, Regulatory Affairs, Operations

Blueprint Medicines is a global precision therapy company that invents life-changing therapies for people with cancer and hematologic disorders. We are looking to hire for a Senior Manager/Associate Director tor the Regulatory Affairs team. The Senior Manager/Associate Director of Regulatory Affairs, Operations is responsible for managing global health authority eCTD submissions for various regions to advance Blueprint Medicines regulatory portfolio and development pipeline. This person will use systems, processes, cross-functional teamwork, and vendor management to ensure timely delivery of business priorities and regulatory results. More information for the Senior Manager position.


Professor, Mechanical Engineering

The Department of Mechanical Engineering at Boston University invites applications for a Professor of the Practice position beginning in July 2021. The successful candidate will be responsible for, and committed to, delivering excellent courses at all levels in Mechanical Engineering, with particular emphasis on advanced courses in engineering design as it relates to manufacturing, product development, and robotics. Applicants for the position must have a Masters or Ph.D. in Mechanical Engineering or a related field. Only individuals with exceptional and unique experiences in industrial or clinical settings that match the teaching needs of the department will be considered for the position. Demonstrated excellence in teaching applicable courses will be considered advantageous, although individuals with a track record of public speaking and industrial leadership will also be entertained. More information for the Professor position.


R&D Intern (Formulation), Lyndra Therapeutics

For the Formulation Intern position, we are seeking a motivated intern who is passionate about changing how patients take medicine. The Formulation Development group uses theoretical principles of chemistry, materials science, and bioengineering coupled with empirical studies to identify and characterize drug delivery components of Lyndra's oral dosage form. Additionally, we aid the process and manufacturing operations of these identified compositions. The intern will report to a Formulation Scientist and work cross-functionally to gain experience across these technical areas and operations. More information about the Intern position.


R&D Co-op (Platform Discovery Engineer), Lyndra Therapeutics

Lyndra Therapeutics is a clinical-stage biopharmaceutical company that has developed the first ultra-long acting pill that lasts a week or longer and can provide a wide range of medicines in a familiar oral capsule form. For the Platform Discovery Engineer Co-op position, we are looking for a motivated co-op who is passionate about changing how patients take medicine. The co-op will work under two engineers spanning the process development and exploratory technologies groups. The main projects will revolve around optimizing the processes we use to create and assemble the various components of Lyndra's novel oral dosage form, as well as the characterization of the platform. The R&D Co-op will work cross-functionally among different teams and will gain experience in a variety of unit operations: hot melt extrusion, infrared welding, cryo-milling, injection molding, 3D printing. Experience with any of these operations is not required but would be a plus. Find more information about the Platform Discovery
Engineer
 position.


R&D Co-op (Analytical Research & Development), Lyndra Therapeutics

Lyndra Therapeutics is a clinical-stage biopharmaceutical company that has developed the first ultra-long acting pill that lasts a week or longer and can provide a wide range of medicines in a familiar oral capsule form.We are seeking a motivated Co-Op to assist with research and development activities in the Analytical Research and Development group. The Analytical Research and Development group is an integral part of Lyndra Therapeutics. The group is responsible for developing, validating, and executing analytical methods, including HPLC, Dissolution / In Vitro Release, Gel Permeation Chromatography etc., for evaluation of the purity, potency, and in vitro release performance of Lyndra dosage forms. Other important applicant skills include Hands-on manufacturing operations skills, the ability to follow and execute instructions, and attention to detail. Find more information about the Analytical Research and Development position.


Regulatory Affairs Intern, Lyndra Therapeutics

Lyndra Therapeutics is a clinical-stage biopharmaceutical company that has developed the first ultra-long acting pill that lasts a week or longer and can provide a wide range of medicines in a familiar oral capsule form. We are seeking an intern to join the Regulatory Affairs/ Quality Assurance (Good Manufacturing Practices - GMP) department. The role will focus on supporting Regulatory Strategy and Operations and will have the opportunity to support the RA organization, program strategies, health authority meeting preparations, and exposure to Program Management and Quality. In this position candidates will assist in the preparation of RA documents and in Assist in the development and/or revision, implementation, and maintenance of policies/ SOPs/ forms to ensure they reflect current practices and are in compliance with FDA and other regulatory requirements and guidance. More about the Regulatory Affairs Intern position.


Manufacturing Co-op/Intern, Lyndra Therapeutics

Lyndra Therapeutics is a clinical-stage biopharmaceutical company that has developed the first ultra-long acting pill that lasts a week or longer and can provide a wide range of medicines in a familiar oral capsule form. Reporting to the Manufacturing Engineer, the co-op/intern will primarily assist with polymer processing via hot-melt extrusion, drying/moisture content studies, and analytical/mechanical testing of Lyndra’s proprietary drug delivery formulations. Applicants will require technical background related to polymer processing, chemical or mechanical production, and/or appropriate experience in manufacturing. Other important applicant skills include Hands-on manufacturing operations skills, the ability to follow and execute instructions, and attention to detail. More information about the Co-op/Intern position.


Associate, Novo Ventures

Novo Ventures is seeking an Associate to support the public equity investing activities of the team in our San Francisco office. The Novo Ventures team is responsible for advising Novo Holdings, a leading global life science investor, on investments in emerging life science companies. A successful candidate will support the public equities Partners in conducting due diligence on potential investment ideas and management of the portfolio. Our public investing activities implement a long-only strategy focused on midcap biotech and MedTech companies driven by science, data, and a long-term view. Efforts in this area are primarily focused on pre-clinical and clinical-stage biotechnology companies as well as high growth revenue stage medical technology opportunities. More information about the Associate position.


Senior Director/Vice President, Therapy Area Lead

Blueprint medicine is a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease. We are looking to hire candidates for the position of Director/ Vice president/ Therapy Area Lead. The Therapy Area Lead (TAL) will be a strategic franchise leader, responsible for establishing the long-term vision, setting strategy, and achieving strong execution across a franchisee of multiple clinical-stage programs. Reporting to the SVP, Head of Portfolio Strategy, the TAL will champion critical portions of Blueprint Medicines’ portfolio with significant executive visibility and potential for patient impact globally. For more information about the Director/ Vice President position.


Medical Science Liaison, Pacific Northwest, Rare Disease/Oncology

Blueprint medicine is a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease. We are looking to hire candidates for the position of Medical Science Liaison. This position is a field-based scientific and clinical expert who strategically supports the medical objectives of Blueprint Medicines’ development programs. The MSL is responsible for identifying, developing, and managing peer-to-peer relationships with a variety of healthcare providers, including oncologists, pathologists, and allergists/immunologists, as well as basic scientists, in academic and community practices. For more information about the Medical Science Liaison position.


Medical Science Liaison, Washington D.C. Metro, Rare Disease/Oncology

Blueprint medicine is a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease. We are looking to hire candidates for the position of Medical Science Liaison. This position is a field-based scientific and clinical expert who strategically supports the medical objectives of Blueprint Medicines’ development programs. The MSL is responsible for identifying, developing, and managing peer-to-peer relationships with a variety of healthcare providers, including oncologists, pathologists, and allergists/immunologists, as well as basic scientists, in academic and community practices. For more information about the Medical Science Liaison position. 


Administrative Intern

Harvard WIT+ seeks an intern who will work directly with the Harvard WIT+ co-chairs to provide a wide range of administrative assistance for our monthly events, website and monthly digest, and our mentoring program. The intern will work both independently and in collaboration with Harvard WIT+ staff volunteers from across the university. Interested candidates should be independently motivated with a demonstrated interest in advancing diversity, equity and belonging who are comfortable with working under minimal supervision. This paid internship is, working 15 hours a week during business hours (flexible based on the intern’s schedule). This is a temporary position and ideally the intern would be able to commit to a year, summer included. For more information about the Administrative Intern position.


Principal/Sr. Scientist, Team Lead - Vector Production; AAV Engineering 

Dyno Therapeutics is reshaping the gene therapy landscape through AI-powered vectors. Efficient production of high-quality vectors remains a critical barrier to realizing the potential of gene therapy, and production of libraries of AAV capsids is central to Dyno’s platform screening strategy. In leading this functional team, you will be responsible for the operation of vector production workflows, measuring capsid properties in high-throughput, supporting the development of novel library designs, and leading the expansion of capabilities to produce high quality AAV vectors at scale. Learn more about the Team Lead - Vector Production position. 


Principal/Sr. Scientist, Program Lead - Gene Therapy; AAV Engineering

Dyno Therapeutics is reshaping the gene therapy landscape through AI-powered vectors. Dyno’s platform is expanding to support Capsid discovery across an array of therapeutic areas. As a Program lead, your role will be to plan and execute the capsid engineering strategy for a focus area such as the CNS, liver, muscle, kidney or eye, with the goal of discovering capsids with transformative potential for delivering gene therapies. Learn more about the Program Lead - Gene Therapy position.