NewSenior Manager, Quality, Standards And Compliance Alnylam Pharmaceuticals, Inc.Senior Manager, Quality, Standards And ComplianceCambridge, MAThe role supports the development and monitoring of Regulatory Sciences compliance metrics, provides compliance oversight and coordination of deviations and CAPAs, and serves as a key liaison with Quality Assurance. Facilitate root cause analysis, CAPA development, implementation tracking, and timely closure of quality events in partnership with accountable Regulatory Sciences process owners.
Senior Director Cell & Genetic Therapies Quality - Personalized Medicine Vertex Pharmaceuticals, IncSenior Director Cell & Genetic Therapies Quality - Personalized MedicineBoston, MA$213,600–$320,400 / yearEstablish compliance governance routines to proactively monitor compliance trends, operational performance, and emerging risks that may impact product quality, patient safety, supply continuity, or program execution; lead or support risk-based mitigation plans, continuous improvement actions, and sustainable process enhancements. Provide strategic Quality Systems leadership in support of personalized medicine /advanced CGT programs, ensuring alignment with CGT Business Objectives, Vertex Global Quality Strategy, commercial priorities, regulatory expectations, and patient-centered outcomes.
Sr. Engineer, Sustaining R&D Olympus CorpSr. Engineer, Sustaining R&DWestborough, MAContributes to all aspects of product development activities and product Design History File, such as requirements creation/documentation, ideation / prototyping, design / development, technical risk mitigation, verification testing and reports, design validation studies, risk management documentation, design reviews, and supports the compilation of documents to enable regulatory submissions. Olympus Corporation of the Americas, a wholly owned subsidiary of Olympus Corporation, is headquartered in Center Valley, Pennsylvania, USA, and employs more than 5,200 employees throughout locations in North and South America.
Senior Director, Analytical Development & Quality Control Rhythm Pharmaceuticals IncSenior Director, Analytical Development & Quality ControlBoston, MA$210,000–$370,000 / yearYou will lead and develop a high-performing organization while overseeing external partners, including CDMOs, CROs, and contract laboratories, to deliver analytical development and QC activities across drug substance and drug product. As the Senior Director, Analytical Development and Quality Control, you will provide strategic and technical leadership for analytical development and quality control across Rhythm's portfolio, spanning discovery through commercialization and lifecycle management.
Senior Engineer - Steam Turbine Leonardo DRS IncSenior Engineer - Steam TurbineFitchburg, MA$102,433–$159,027 / yearSeveral factors can influence the pay scale, including but not limited to: Federal contract labor categories and contract wage rates, collective bargaining agreements, geographic location, business considerations, scope, and responsibilities of the position, local or other applicable market conditions, and internal equity. Use of modern computational turbomachinery design-oriented tools as supplemented by comprehensive understanding of the first order and analytical models relevant to steam turbine design will be critical to the success of this position.
Quality Senior Specialist - Finished Goods – Commercial (Contract) 500 Vertex PharmaceuticalsQuality Senior Specialist - Finished Goods – Commercial (Contract) 500Boston, Massachusetts$55–$65 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Experience leading complex projects/teams and continuous improvement initiatives within stated objectives and timelines; effectively applies project management processes / tools to lead meetings, assist with project planning, and facilitate completion of tasks.
Product Disposition Sr. Specialist, Quality The Steely GroupProduct Disposition Sr. Specialist, QualityBedford, MAThe Senior Specialist, Product Disposition will support the timely and compliant disposition of all the company Gene Therapy products across all stages of manufacturing. The Senior Specialist will bring strong attention to detail, a quality-first mindset, and the ability to work cross-functionally in a fast-paced, regulated environment.
Senior Manager, Quality Control Stoke Therapeutics IncSenior Manager, Quality ControlBedford, MA$172,000–$192,000 / yearManager, Quality Control (QC) is responsible for overseeing all aspects of GMP testing and supporting stability program management for Stoke' IMPs at Stoke's Contract Testing Laboratories (CTLs) / Contract Manufacturing Organizations (CMOs). Oversee day-to-day management of outsourced GMP release testing at various CTLs / CMOs to ensure successful and compliant execution of laboratory operations to meet GMPs, regulatory requirements, guidelines, internal policies, and procedures.
NewAnalytical Science and Technology Senior Scientist Vertex PharmaceuticalsAnalytical Science and Technology Senior ScientistBoston, Massachusetts$120,000–$180,000 / yearWe seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
NewSenior Supplier Quality Engineer Repligen CorpSenior Supplier Quality EngineerMarlborough, MACross-Functional Partnership: Collaborate with Quality, Sourcing, Engineering, Operations, and Regulatory teams on supplier qualification, product and process validation, supplier changes, and quality improvement activities. Supplier Risk and Development: Perform supplier risk assessments and support development plans for key and critical suppliers to reduce quality and supply risk and improve supplier capability.
NewGMP Operational Quality Senior Manager (Contract) 820 Vertex PharmaceuticalsGMP Operational Quality Senior Manager (Contract) 820Boston, Massachusetts$85–$90 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Demonstrated ability to evaluate quality matters and make complex decisions leveraging technical experience and advanced judgement and the analysis/synthesis of a variety of information; able to work outside of precedent and takes a new perspective on existing solutions.
NewAnalytical Science And Technology Senior Scientist Vertex Pharmaceuticals, IncAnalytical Science And Technology Senior ScientistBoston, MA$120,000–$180,000 / yearKnowledge and Skills: Demonstrated expertise in analytical method development, characterization, and qualification/validation for biologicsKnowledgeable in ICH/USP/EMA guidelines with a strong GMP background, CGT related preferredExperience managing contract (CTO/CDMO) analytical testing, highly desirableExperience with technical support of commercial biological products and cGMP manufacturingAbility to prioritize objectives from multiple projects and adhere to scheduled timelines while maintaining flexibility and efficiencyExcellent technical writing skills, and communication skills with the proven ability to build open and collaborativeHands-on experience with methods related to CGT products, prefer in-vitro cell-based functional, potency and/or microbiology assays. Key Duties and Responsibilities: Accountable for the success of commercial analytical activities, prioritization, and execution to meet program commitmentsSubject Matter Expertise (SME) for ensuring the robustness of analytical methods and commercial testing requirementsAuthor and/or review technical documents, including method SOP, study protocol and technical reportPartners effectively with internal and external functions for commercial analytical technology transferPrimary responsibilities extend to analytical method validations, continuous improvement, and lifecycle managementCollaborate with Vertex cross-functions, including Analytical Development, Process Development, Commercial Manufacturing, Supply Chain, Quality teams, Vertex Partners, and Contract Test labs.
Senior Digital Electrical Engineer Teledyne TechnologiesSenior Digital Electrical EngineerBillerica, Massachusetts$113,600–$151,400 / yearThese markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.. Our arsenal includes advanced surveillance sensors, handheld devices, unmanned vehicles, lasers, and more solutions that increase operational effectiveness for warfighters, first responders, and search-and-rescue teams.
Senior Therapeutic Area Specialist, Neuroscience - Cobenfy - Boston, MA Bristol Myers SquibbSenior Therapeutic Area Specialist, Neuroscience - Cobenfy - Boston, MABoston, MA$139,230–$168,714 / yearAs this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of "Qualified Driver," as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver's license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Sr. Director, TA Lead - Trial Analytics, Insights, And Planning (Taip) Bristol Myers SquibbSr. Director, TA Lead - Trial Analytics, Insights, And Planning (Taip)Cambridge, MA$261,840–$317,292 / yearThe TAIP TA Lead is a senior leadership role reporting directly to the Head of the TAIP unit within Bristol Myers Squibb's Trial Analytics, Insights, and Planning (TAIP) organization-an internal consulting team that drives clinical development excellence through data-driven insights, feasibility modelling, and strategic trial planning. As the analytics lead for the Oncology therapeutic area (TA), you will be accountable for the end-to-end analytics strategy and execution across a global portfolio of clinical trials within that TA-supporting trial-level planning, overseeing delivery performance, and leading a team of analytics professionals across multiple levels and geographies.
Senior Technical Program Manager InterSystemsSenior Technical Program ManagerBoston, Massachusetts$127,000–$157,000 / yearPlease note that the use of wearable technology, including any AI-related tools or other technology-connected devices (such as META or Google smart glasses and/or wearables, and/or any similar devices), is strictly prohibited during the interview and screening process with InterSystems. Our data platforms solve interoperability, speed, and scalability problems for large organizations around the globe to unlock the power of data and allow people to perceive data in imaginative ways.
Senior Project Engineer Mantis Innovation Group LLCSenior Project EngineerBurlington, MA$120,000–$140,000 / yearWe look at the entire facility-inside and out-and can impact 70% of what a building operator allocates critical budget dollars toward, including: Strategic electricity and natural gas procurement, renewable energy, and demand response; climate impact reduction and reporting, net zero strategies, and sustainability planning; roofing, solar, HVAC assessment management, pavement, building envelope, data center optimization, and EV charging; lighting/LED retrofits, HVAC/mechanical systems, and BMS/BAS improvements and implementation. Client sites may include industrial facilities, commercial buildings, utility plants, mechanical rooms, construction sites, production areas, rooftops, and other operational environments.
Senior Data Engineer - Translational Data Products Bristol-Myers Squibb CoSenior Data Engineer - Translational Data ProductsCambridge, MA$118,650–$143,778 / yearOur team builds and maintains data products that make R&D data usable and AI-ready: biomarker, biospecimen, clinical trial, omics, among others, assembled into governed, curated, linked, documented, AI-ready products that translational scientists and analysts use for insight generation and decision making. Engage stakeholders in translational medicine, biomarker sciences, predictive medicine, reverse translation and clinical development to understand and translate the high value questions they are trying to answer into robust data product designs and data maps linking sources to targets (STTM).
Senior Principal Scientist, Neuroscience, Clinical Biomarker, Late Phases, Translational Medicine Bristol-Myers Squibb CoSenior Principal Scientist, Neuroscience, Clinical Biomarker, Late Phases, Translational MedicineCambridge, MA$184,060–$223,036 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Key Responsibilities: Designs and implements program-specific late development biomarker/translational plans, responsible for aiding in creation of clinical protocols, SAPs, SOWs, lab manual, and interfacing with CRO for execution of services, in conjunction with Biospecimen Operations and Procurement.
Senior Technical Staff Engineer - Quality (Supplier) Microchip Technology IncSenior Technical Staff Engineer - Quality (Supplier)Beverly, MA$91,000–$247,000 / yearPreferred Qualifications: Special processes (Laser Weld, Plating), J-STD-001, IPC-A-610, IPC-A-620, Risk Mitigation Strategies, AS9102, GD&T, RCCA, GD&T, J-STD-001, J-STD-002, Wire Crimping, Soldering, RCCA, special process audits, SPC, Systemic CA, Supplier Development, Drive Improvements with Suppliers. The successful candidate will be responsible for overseeing a small Supplier Quality Engineering (SQE) team located across the US and EU, supporting MCHP's Systems factories, with direct responsibility for supporting the Beverly factory.