Jounce Therapeutics

Job Listings

Here are our current job openings. Please click on the job title for more information, and apply from that page if you are interested.

The system cannot access your location for 1 of 2 reasons:
  1. Permission to access your location has been denied. Please reload the page and allow the browser to access your location information.
  2. Your location information has yet to be received. Please wait a moment then hit [Search] again.


Jounce Therapeutics, Inc. is a clinical-stage immunotherapy company dedicated to transforming the treatment of cancer by developing therapies that enable the immune system to attack tumors and provide long-lasting benefits to patients through a biomarker-driven approach. Jounce currently has multiple development stage programs ongoing while simultaneously advancing additional early-stage assets from its robust discovery engine based on its Translational Science Platform. Jounce’s most advanced product candidate, vopratelimab, is a monoclonal antibody that binds to and activates ICOS, and is currently being studied in the SELECT Phase 2 trial. JTX-4014 is a PD-1 inhibitor intended for combination use in the SELECT trial and with Jounce’s broader pipeline. Jounce’s next development stage product candidate, JTX-8064, is a LILRB2 (ILT4) receptor antagonist shown to reprogram immune-suppressive tumor associated macrophages to an anti-tumor state. A Phase 1 trial evaluating JTX-8064 is planned to begin enrollment in the fourth quarter of 2020. Additionally, Jounce exclusively licensed worldwide rights to JTX-1811, a monoclonal antibody targeting CCR8 and designed to selectively deplete T regulatory cells in the tumor microenvironment, to Gilead Sciences, Inc. For more information, please visit www.jouncetx.com. www.jouncetx.com

Jounce is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.

All applicants should be legally entitled to work for any employer in the U.S.

Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.

Click column header to sort

Page 1 of 1

The Protein Production Group at Jounce Therapeutics is looking for an individual experienced in mammalian cell culture, protein purification, and characterization. The successful candidate will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology.  You will be responsible for the production and purification of antibodies and other proteins for use in R&D that will enable the development of groundbreaking therapies. You will be expected to participate in experimental design, conduct experiments, optimize throughput, and maintain detailed records. You will also have the opportunity to represent the Protein Prodution Group on cross-functional program teams and guide programs to development candidate nomination. This is an exciting opportunity to be part of a collaborative and fun team within the fast-paced and dynamic field of immuno-oncology.   Responsibilities: - Transient protein production in mammalian cell lines - Protein purification including affinity chromatography, ion-exchange chromatography and size-exclusion chromatography - Protein characterization methods including SE-HPLC, SDS-PAGE, and endotoxin assays - Employing liquid handling robots in the protein production process at smaller scales - Utilizing automated platforms to generate transfection-grade plasmid DNA - Thorough documentation and cross-functional communication
Job ID
2021-1262
Location
US-MA-Cambridge
Jounce is looking for an Associate Scientist/ Senior Associate Scientist specializing in in vitro biology to join our Discovery Immuno-Oncology team. The successful candidate will be an experienced and highly motivated laboratory researcher engaged in the discovery and testing of novel cancer immunotherapeutic biologics. S/he will generate data to identify and support advancement of new projects into the Discovery pipeline and will be expected to participate in decision-making by sharing her/his expertise and perspective. Responsibilities include designing, developing, and conducting experiments aimed at identifying candidates for antibody therapeutics. S/he will have the opportunity to work independently and collaboratively to discover and advance new programs in a dynamic and fast-paced environment.   Responsibilities: - Development and trouble shooting of immune cell-based assays to validate the immunomodulatory activity of candidate therapeutics. Assay development will require human primary immune cell isolation as well as cell line engineering. - Data analysis and interpretation, thorough documentation of work, and clear communication of results in group settings. - Active participation in interpretation and assessment of data across the Discovery organization. - Work cross-functionally as part of internal multi-disciplinary project teams - Maintain a safe and clean laboratory environment following all precautions for working in a BSL2/BSL2+ laboratory.
Job ID
2021-1261
Location
US-MA-Cambridge
The Clinical Pharmacology Team at Jounce is hiring! We are seeking a bioanalytical scientist to oversee the development and implemention of large molecule drug concentration, anti-drug antibody (ADA), and neutralizing antibody (Nab) assays in animal and human serum from the IND-enabling development stage through filing. The successful candidate will have 2-4 years’ experience developing or outsourcing development of regulated bioanalytical assays for biologics, familiarity with multiple ligand-binding assay platforms, and an understanding of regulatory requirements and emerging trends related to bioanalysis. A key component of this role is to manage relationships with CROs and ensure they are delivering high quality data in a timely fashion and in compliance with regulatory standards. The ideal candidate will be collaborative with the ability to work cross-functionally, to effectively communicate with key stakeholders, and to participate on cross-functional teams.   - Work with internal colleagues to ensure generation of appropriate assay reagents for preclinical and clinical bioanalytical assays; - Select appropriate bioanalytical assay vendors for IND-enabling PK, PK/PD and toxicology studies as well as clinical studies for molecules entering development; - Oversee technical aspects of assay development and validation at the vendor; - Review and sign off on method development reports, validation plans, validation reports, sample analysis plans, and sample analysis reports; - Oversee sample analysis to ensure adherence to budget, timelines and regulatory guidelines; - Oversee and manage inventories of critical reagents within Jounce and at the assay vendors; - Perform quality control review of assay performance and sample data; - For clinical samples, work with clinical operations, clinical pharmacology, and data managmenet colleagues to establish sample analysis timelines and budgets, create statements of work (SOWs) and data transfer agreements (DTAs), and file vendor communication records in the trial master file (TMF); - Oversee drug interference testing and update assays and validations as needed during the lifecycle of a molecule to ensure stage-appropriateness and compliance with emerging regulatory standards; - Support vendor audits and technical reviews; - Participate in regulatory document preparation (briefing books, eCTD modules) and poster/manuscript writing; and - Provide technical expertise on cross-functional teams.
Job ID
2021-1260
Location
US-MA-Cambridge
The Clinical Pharmacology Team at Jounce is hiring! We are seeking a motivated early-career pharmacometrician for a hand’s on role performing PK and pharmacometric analyses to support the development of novel immuno-oncology biological therapeutics. The successful candidate will support projects from discovery through clinical development with quantitative analyses to support candidate selection/optimization and selection of the first-in-human dosing range and recommended phase 2 dose, and conduct exposure/response analyses to support internal decision-making and BLA filings. The incumbent will also have the opportunity to represent clinical pharmacology in project team and subteam meetings and participate in meetings with senior management and regulatory authorities as part of a growing function at Jounce.   - Provide pharmacokinetic and pharmacometric support from discovery through clinical development for large molecule therapeutics; - Analyze preclinical and clinical PK data using industry-standard software; - Support Discovery Project Teams during lead optimization and candidate selection to identify key aspects of target biology impacting PK properties and PD response; contribute to efforts to optimize candidate characteristics accordingly; - Partner with in vivo translational and bioanalytical scientists to design and conduct preclinical PK, PK/PD and biodistribution studies, and perform PK/PD analyses to delineate exposure-response relationship; - Develop strategies for first-in-human clinical starting dose and dose range selection, utilizing appropriate allometric scaling and modeling methodologies where appropriate; - Create pharmacometric plans and PK/pharmacometric analysis plans; - Collaborate with programming and data management to collect data and prepare analysis datasets; - Perform and/or oversee outsourced performance of population PK, population PK/PD, and exposure/response modeling for clinical stage asset; - Present PK and pharmacometric results and recommendations internally at cross-functional Project Teams, relevant subteams, and Portfolio Steering Committee; - Write/review preclinical PK and PK/PD reports, clinical pharmacometric reports, and dose selection reports; contribute to the clinical pharmacology portions of clinical protocols, investigator brochures, and clinical study reports; - Participate in preparation of regulatory briefing books, regulatory responses, INDs, and BLAs; participate with supervision in interactions with regulatory agencies; - Standardize procedures for PK and pharmacometric dataset preparation and analyses, including identifying and creating necessary SOPs or work practices; and - Represent clinical pharmacology at cross-functional teams including Project Teams and relevant subteams.
Job ID
2021-1259
Location
US-MA-Cambridge
The Medical Affairs team at Jounce is hiring! We are seeking a Medical Science Liaison. Jounce has had a strong Medical Science Liaison (MSL) team to support our advancing clinical and research programs since 2019.  The MSL position is an exciting opportunity to join a company dedicated to transforming the treatment of cancer by developing therapies that enable the immune system to attack tumors and may bring long lasting benefits to patients. The MSLs are highly trained Medical Affairs (MA) professionals with strong clinical and/or scientific backgrounds.     We expect MSLs to have excellent communication and presentation skills. MSLs should demonstrate a solid understanding of immune-oncology as a therapeutic disease area as well as knowledge of clinical trial sites and/or connections with oncology experts. The Medical Science Liaison functions as a field-based, scientific expert who engages health care professionals to exchange clinical, scientific, and research knowledge. By following regulatory and corporate guidelines, they will facilitate and build scientific relationships and collaborations with the medical/scientific community as well as support clinical study initiatives (including patient enrollment in clinical trials). This position interacts with local, regional, and national HCPs; societies; and organizations. Due to the early stage of development of multiple compounds, the MSL will be utilized heavily in supporting clinical operations and clinical development.    In addition to a world-class research organization, Jounce prides itself on a solid translational and reverse translation approach to clinical trials.  Currently (though that may change in the future), the focus is mostly on early clinical development (phase 1 and 2).  MSLs will need to have a solid understanding of translational approaches within clinical studies while interacting with key clinical experts in the field.    - Function as the primary point of contact in the field for Jounce Medical Affairs.  - Maintain clinical, scientific, and technical expertise in relevant Immuno-Oncology/Oncology disease state areas.  - Have a thorough understanding of Jounce clinical protocols and related procedures.  - Collaborate with clinical operations and clinical development to support the recruitment of clinical trials, identify potential new clinical trial sites, and serve as an on-site Jounce resource to study site staff participating in Jounce studies.   - Execute study enrollment plans and clinical trial site engagement activities.  - Develop and track key opinion leader (KOL) engagement plans - identify, develop, and maintain long-term collaborative relationships with KOLs within assigned region. Participate in medical & scientific exchanges with the medical/scientific community including advisory boards.  - Respond to and document unsolicited requests for information on Jounce clinical programs.  - Facilitate company sponsored trials and serve as a resource for investigator sponsored trial (IST) proposals. Provide medical/clinical teams with feedback and insights from interactions with KOLs and investigators.  - Facilitate research collaborations with key investigators including helping identify, establish, and maintain such collaborations.   - Represent the company at medical meetings through Medical Affairs’ Scientific Booth coverage and other related activities.  - Adhere to corporate SOPs and ensure vigilant compliance with relevant legal and regulatory guidelines governing scientific interactions with physicians and healthcare professionals across all activities, including those related to clinical trials, scientific interactions with internal and external groups, and responses to unsolicited requests for medical/scientific information.  - Consistently demonstrate a high standard of excellence in the management of assigned territory while also contributing to the success of colleagues and the MSL organization.  - MSLs must contribute to the achievement of organizational goals beyond the borders of a geographic territory. 
Job ID
2021-1257
Location
US-
Jounce Therapeutics is seeking an experienced translational immunologist to join the Translational Exploratory and Clinical Immunology team and contribute to the development of novel cancer immunotherapies. The successful candidate will be responsible for managing multiple aspects of biomarker assays in on-going clinical trials. They will be applying Flow Cytometry and other immunoassays to develop and execute on a predicative and pharmacodynamic biomarker strategy. As part of a multi-disciplinary team, they will be expected to proactively interact with project teams, external collaborators and drive lab-based research to bring best-in-class biomarker strategies to Jounce clinical programs. - Contribute scientific leadership to Jounce clinical programs, representing function within larger program team for vopratelimab development. - Gain subject matter expertise for on-going clinical biomarker assays for vopratelimab development in the SELECT trial and beyond. - Work cross-functionally within Research to identify and establish assays and technologies to support mechanistic studies and biomarker validation. - Manage and guide the development of SOPs for the central lab; manage the scientific review, QC and presentation of external vendor results. - Contribute to scientific rationale for combination strategy for Jounce pipeline programs. - Train and continuously develop scientists and associates in the Translational Exploratory Immunology group.
Job ID
2021-1256
Location
US-MA-Cambridge
This individual will report to the Chief Financial Officer and work closely with the executive team to establish and implement a successful Investor Relations strategy that articulates and supports the Company's business and scientific objectives to the investment community and other external audiences including the scientific community. They will also manage all external communications, including media and public relations (news and editorial coverage, press releases and articles); financial communications, strategic executive communications; and Company website communications. Will act as a Company spokesperson, promoting, enhancing, and projecting the organization's vision, brand and reputation to external stakeholders, with a primary focus on analysts and investors, and build new and manage existing relationships with the investment community and other outside influencers. - Continue to develop Jounce’s investor relations program to ensure a consistent, timely flow of information about Jounce to the investment communities and Company shareholders. Establish and maintain excellent relations with institutional investors, key retail investors and analysts - Understand the science, technology, pipeline and business strategy sufficiently to identify issues and effectively communicate with investors - Partner with the CEO, CMO and CFO to lead and manage the Company's participation on quarterly earnings calls, investment conference calls and in-house meetings, road shows, analyst days, and one-on-one meetings - Develop relationships and maintain regular communication with individual investors, covering analysts and select buy-side contacts to provide up to date information about events and market trends affecting the Company, with the goal of communicating our long-term vision - Manage the Company's corporate communications via the Company website, social media channels, etc. Update and continuously improve the corporate website and social media efforts ensuring that key messages and communications are consistent - Lead strategic communications development, including, developing communications plan to take advantage of key Company milestones, preparing press releases, presentation decks, and earnings releases, creating management Q&As, conference call scripts, and business descriptions/other information for securities filings, and the Company website - Serve as a primary person to handle incoming inquiries from the media and investors - Establish strong internal relationships and effective communication with supporting business, scientific, and medical leadership within the organization - Manage an external set of advisors to successfully meet group objectives - Person should be comfortable with being hands-on and operating within a lean budget
Job ID
2021-1255
Location
US-MA-Cambridge
The Office Administration team at Jounce is hiring! We are seeking an Office Administrator who will serve as the first point of contact for the Company and will set the tone of the reception area for visitors. She/he will be responsible for the office environment including managing supplies, ordering food and organizing companywide events. The ideal candidate will be warm, welcoming, outgoing and highly organized. This position requires polished communication skills, exceptional attention to detail, good judgment, and the ability to manage within a very dynamic, fast-paced environment, with constantly evolving priorities. We are looking for a team player who is energetic, proactive and hardworking. This role will require onsite presence 5 days a week during business hours (9 a.m. – 5 p.m. ET). - Greet, register and direct visitors to appropriate parties; active presence at the front desk for majority of the workday required. - Answer phones and direct calls accordingly. - Sort and deliver incoming mail. - Track, order and maintain storage areas for office supplies. - Manage food and kitchen supply program including monitoring and ordering snacks and groceries, receiving and unpacking weekly and daily food deliveries, and overall upkeep of refrigerators and snack area. - Collect, organize and update content for Company intranet site. - Assist Human Resources with onboarding/offboarding process. - Create and maintain security badges. - General administrative team and back-up support. - Assist with companywide events including happy hours, Company meetings, offsites, etc. and responsible for conference room and common area upkeep. - Order swag for new hires and companywide events / yearly Company gift.
Job ID
2021-1254
Location
US-MA-Cambridge
The Protein Production Group at Jounce Therapeutics is looking for an individual experienced in mammalian cell culture, protein purification, and characterization. The successful candidate will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology.  He/she will be responsible for the production and purification of antibodies and other proteins for use in R&D that will enable the development of groundbreaking therapies. He/she will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and participate in cross-functional collaborations.  This is an exciting opportunity to be part of a collaberative and fun team within the fast-paced and dynamic field of immuno-oncology.   Responsibilities: - Transient protein production in mammalian cell lines - Protein purification including affinity chromatography, ion-exchange chromatography and size-exclusion chromatography - Protein characterization methods including SE-HPLC, SDS-PAGE, and endotoxin assay - Employing liquid handling robots in the protein production process at smaller scales - Utilizing automated platforms to generate transfection-grade plasmid DNA - Thorough documentation and cross-functional communication
Job ID
2021-1251
Location
US-MA-Cambridge
Jounce Therapeutics is seeking an experienced translational scientist to join the Translational Pathology team and contribute to the development of novel cancer immunotherapies. The successful candidate will be responsible for managing multiple aspects of preclinical and clinical development of biomarker assays and applying histologic techniques and image analysis to better understand the tumor micro-environment. As part of a multi-disciplinary team, they will be expected to proactively interact with project teams and external collaborators to provide insights and brainstorm ideas on how histologic techniques can be applied to advance Jounce programs.   Responsibilities: - Contribute scientific and subject matter expertise to Jounce programs from early discovery to clinical stage. - Provide insights and support in histology, immunohistochemistry, RNA in situ hybridization and other tissue-based assays to programs. - Work cross-functionally with other Research functions to identify and establish assays and technologies to support mechanistic studies and biomarker validation. - Lead improvement of current processes withing the Pathology groups, and evaluate novel technologies and modalities with the potential to impact Jounce discovery platform and pipeline. - Manage and guide the development of SOPs for the central lab; manage the scientific review, QC and presentation of external vendor results.  - Write, update, and provide training on laboratory SOPs, provide input on SAP, and data transfer agreements and clinical study reports.  - Train and continuously develop scientists in the pathology group. 
Job ID
2021-1249
Location
US-MA-Cambridge
Jounce is looking for an experienced Associate Scientist/ Senior Associate Scientist specializing in In Vitro biology to join our Discovery Immuno-Oncology team. The successful candidate will be an experienced and highly motivated laboratory researcher engaged in the discovery and testing of novel cancer immunotherapeutic biologics. S/he will generate data to support key decisions for project teams and will also participate in the decision-making by sharing her/his expertise and perspective. Responsibilities include designing, developing, and conducting experiments aimed at identifying optimal therapeutic candidates and understanding the mechanism of action of our therapeutic molecules (mostly monoclonal antibodies). S/he will have the opportunity to work independently and collaboratively to advance portfolio programs in a dynamic and fast-paced environment.   Responsibilities: - Perform various in vitro immune cell culture assays, immunophenotyping by multi-color flow cytometry, intracellular cytokine staining, ELISA and multiplex technologies, proliferation assays and primary immune cell isolation - Perform screening assays for therapeutic lead selection - S/he will be responsible for data analysis, thorough documentation of work, and clear communication of results in group settings - Work cross-functionally as part of internal multi-disciplinary project teams - Maintain a safe and clean laboratory environment following all precautions for working in a BSL2/BSL2+ laboratory.
Job ID
2021-1247
Location
US-MA-Cambridge
The Protein Analytical group at Jounce Therapeutics is looking for an individual with expertise in antibody therapeutics, especially in the fields of antibody characterization/developability assessment and biophysical characterization.   This is an exciting opportunity to play an important role in the discovery and development of novel biotherapeutics for immuno-oncology.  The successful candidate will be the protein analytical lead on project teams, lead experimental design, conduct experiments, optimize throughput, maintain detailed records, develop new technology, and generate standard operating procedures and reports.  In this role you will have the opportunity to work cross functionally across multiple departments including discovery/biology, pre-clinical, Ab technology, protein production and CMC.The ideal candidate will have strong protein biochemistry and antibody discovery knowledge and be proficient at designing and executing lab experiments.   Responsibilities: - Act as key point person in protein characterization/developability assessment teams - Be the protein analytical lead on project team to provide analytical support and participate and present in project meetings. - Monitor and maintain equipment and instruments regularly to ensure proper operation and calibration. - Prepare SOPs and reports - Independently lead and develop new experiments, technological or scientific processes - Proactively share skills/knowledge with others to broaden company capabilities - Take a leadership role within the lab - 75% Laboratory based
Job ID
2021-1246
Location
US-MA-Cambridge
The Protein Analytical group at Jounce Therapeutics is looking for an individual with experience in protein characterization and antibody developability assessment. The successful candidate will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology.  He/she/they will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and generate standard operating procedures.  This is an exciting opportunity to play an important role in the discovery and development of novel biotherapeutics for immuno-oncology.  In this role you will have the opportunity to work cross functionally across multiple departments including discovery/biology, pre-clinical, Ab technology, protein production and CMC. The ideal candidate will have protein biochemistry and antibody discovery knowledge and be proficient at designing and executing lab experiments.   Responsibilities - Act as key point person in protein characterization/developability assessment teams - Monitor and maintain equipment and instruments regularly to ensure proper operation and calibration. - Prepare SOPs and reports - Independently lead and develop new experiments, technological or scientific processes - Proactively share skills/knowledge with others to broaden company capabilities - Take a leadership role within the lab - 100% laboratory based
Job ID
2021-1245
Location
US-MA-Cambridge
Jounce Therapeutics is looking a for a Senior Specialist, Quality Assurance to join a highly experienced team dedicated to transforming the treatment of cancer. The ideal candidate will have a strong understanding of regulatory requirements and industry standards to support daily GxP activities for clinical stage programs. This position will own Employee Training and spearhead document control and batch records across clinical programs.   Requirements: - Lead QA Document Control and GxP Employee Training records through collaboration with key stakeholders in identifying phase-appropriate SOPs, and continued development of GxP employee training program. - Contribute to the generation, review and/or approval of internal and external documents used in GMP activities such as, but not limited to, master batch records, stability protocols/ reports, specifications, deviations, change controls etc. - Perform batch disposition and other relevant document management activities - Track and monitor QA performance metrics and data to drive continuous improvements of internal processes. Generate and evaluate data to support Key Performance Indicators. - Provide QA CMC Operations support for end to end supply chain coverage. This includes quality & compliance support of manufacturing, testing, packaging/ labeling and distribution activities by CMOs for Jounce’s drug substance and drug product global operations (i.e., Product Specifications, Batch Records, Deviations, Investigations, Change Control, QA Lot Disposition, Stability, Retest/Expiration Extensions, termperature excursions, Analytical Method Qualification/Validation). - Ensure that Jounce products meet defined quality standards through batch record review and facilitation of product-related investigations.  - Support external vendor audits, including oversight of vendor management program as needed. - Support eQMS implementation and converstion of current QMS to eQMS in a streamlined process to include training of systems - Other QA related job duties as needed with shifting of priorities - Minimum of Bachelor's degree in science (e.g., biology, chemistry, pharmacy, medical, engineering or related field).
Job ID
2021-1244
Location
US-MA-Cambridge
The ideal candidate will oversee laboratory activities for the discovery and evaluation of novel cancer immunotherapeutic candidates. This person will play an integral role in conducting experiments to support pre-clinical and clinical teams, evaluating and implementing new technologies, and supervising junior lab members.   Responsibilities: - Ensures oversight of the Translational Genomics lab, including directly supervising one scientist. - Contributes expertise to experimental design and conducts translationally focused studies to support drug programs. - Develops and implements RNA and DNA based technologies and establishes QC metrics for the group. - Responsible for the development of assays to be used as potential predictive and pharmacodynamic biomarkers. - Responsible for data analysis, documentation of the work, and clear communication of results in group settings. - Drives technical innovation within the genomics space across multiple platforms, including single cell genomics and GeoMx. - Acts as subject matter expert for clinical application of genomics technologies and analytical tools. - Assists with budgeting, forecasting and project coordination for the lab. - Facilitates working relationships with CROs to outsource or collaborate on technical development efforts.
Job ID
2021-1243
Location
US-MA-Cambridge
The Associate Director, CMC Lead at Jounce Therapeutics will be responsible for managing the outsourced development and manufacturing operations of biologics to contract manufacturers. Successful execution of this role requires a strong scientific approach and established expertise in therapeutic process development or manufacturing.   The responsibilities include: - Support CMC Operations team with CRO/CMO project management - Assist in planning, writing and reviewing CMC sections across all regulatory submissions in a uniform style and language for regulatory compliance - Reviews ancillary CMC documents and reports for completeness and accuracy and for compliance with regulations - Assist in the timely and accurate assembly of responses to inquiries from regulatory agencies on CMC content of regulatory submissions - Lead or participate in Project and CMC development teams, as required. - Establish effective working relationships within Jounce functions, including Research, Regulatory, Quality Assurance and Legal departments - Execution and documentation of experiments in cell line development, bioreactor operation, or purification of biologics in support of technology and drug development
Job ID
2021-1232
Location
US-MA-Cambridge