Sr Manager, QA Operations Emergent BioSolutions IncSr Manager, QA OperationsCanton, MA$171,500–$207,500 / yearUnsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions' approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency. This role is accountable for real time QA oversight of manufacturing operations, lifecycle management of deviations, CAPAs, change controls, validation activities, and risk management, while operating as a key Quality decision-maker independent of Production, consistent with CGMP requirements.
Director/Senior Director, CMC Operations Beam Therapeutics IncDirector/Senior Director, CMC OperationsCambridge, MA$210,000–$320,000 / yearLead the preparation of source documentation and technical review of CMC sections for global regulatory submissions specifically focusing on Module 3. Act as the CMC subject matter expert during regulatory meetings and support information requests from regulatory agencies. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
Senior Manager, Global Regulatory Affairs CMC 3316 Takeda Development Center AmericasSenior Manager, Global Regulatory Affairs CMCBoston, MassachusettsThis role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: This role is within in the GRA Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: With some supervision, leads the execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Senior Director Process Excellence - Global Business Services Cabot CorporationSenior Director Process Excellence - Global Business ServicesBillerica, Massachusetts$228,700–$331,600 / yearCabot is seeking a Senior Director of Process Excellence who will be leading the Process Excellence organization within Cabot’s Global Business Services (GBS) function, and will be responsible for developing and executing Cabot’s end-to-end process strategy, with the ultimate goal of driving GBS service efficiency across end-to-end processes (Record to Report R2R, Order to Cash O2C, Source to Pay S2C and Plan to Deliver P2D). This policy, however, shall not apply to instances in which an employee who has access to the compensation information of other employees or applicants as part of that employee's essential job functions (such as in payroll or HR) discloses the compensation of such other employees or applicants to individuals who do not otherwise have access to such information, unless that disclosure is in response to a formal complaint or charge, in furtherance of an investigation, proceeding, hearing or other action, including an investigation conducted by Cabot, or otherwise as required by law.
Lead Process Operator, Battery Materials – 3rd Shift Premium Billerica, MA Cabot CorporationLead Process Operator, Battery Materials – 3rd Shift Premium Billerica, MABillerica, MassachusettsThis policy, however, shall not apply to instances in which an employee who has access to the compensation information of other employees or applicants as part of that employee's essential job functions (such as in payroll or HR) discloses the compensation of such other employees or applicants to individuals who do not otherwise have access to such information, unless that disclosure is in response to a formal complaint or charge, in furtherance of an investigation, proceeding, hearing or other action, including an investigation conducted by Cabot, or otherwise as required by law. Our strength in research and development is a major reason why we have been an industry leader for more than 135 years in products such as reinforcing and specialty carbons, battery materials, aerogel, fumed metal oxides, inkjet colorants, masterbatches and conductive compounds.
Medical Laboratory Technologist CLS/MLT MFM HealthMedical Laboratory Technologist CLS/MLTMiddleton, MAFull timeCommunicate effectively with providers and clinical staff, including nursing and medical assistants, to support safe and effective specimen collection and testing workflows. The Medical Laboratory Technologist performs moderate-complexity testing only and must not perform high-complexity testing unless specifically trained, qualified, and authorized in accordance with regulatory requirements.
General Medical Technologist Nursing Pro StaffingGeneral Medical TechnologistBoston, MassachusettsYour duties encompass, but are not limited to, the following: Performing Diverse Tests: Conducting a variety of tests on biological specimens and environmental samples using both manual and automated methods. In this multifaceted role spanning various disciplines, including chemistry, hematology, coagulation, urinalysis, and microbiology, you will be responsible for conducting tests and analyzing a wide range of biological specimens.
Lead Process Operator, Battery Materials - 3rd Shift Premium Billerica, MA Cabot CorpLead Process Operator, Battery Materials - 3rd Shift Premium Billerica, MABillerica, MAThis policy, however, shall not apply to instances in which an employee who has access to the compensation information of other employees or applicants as part of that employee's essential job functions (such as in payroll or HR) discloses the compensation of such other employees or applicants to individuals who do not otherwise have access to such information, unless that disclosure is in response to a formal complaint or charge, in furtherance of an investigation, proceeding, hearing or other action, including an investigation conducted by Cabot, or otherwise as required by law. Our strength in research and development is a major reason why we have been an industry leader for more than 135 years in products such as reinforcing and specialty carbons, battery materials, aerogel, fumed metal oxides, inkjet colorants, masterbatches and conductive compounds.
Sr. Global Project Manager Cabot CorpSr. Global Project ManagerBoston, MAThis policy, however, shall not apply to instances in which an employee who has access to the compensation information of other employees or applicants as part of that employee's essential job functions (such as in payroll or HR) discloses the compensation of such other employees or applicants to individuals who do not otherwise have access to such information, unless that disclosure is in response to a formal complaint or charge, in furtherance of an investigation, proceeding, hearing or other action, including an investigation conducted by Cabot, or otherwise as required by law. The Senior Global Project Manager is responsible for leading large, complex and high-value projects across multiple regions, ensuring alignment with business strategy and delivering results safely, on time, within scope, and on budget.
GBS Process Excellence Senior Director Cabot CorpGBS Process Excellence Senior DirectorBoston, MA$228,700–$331,600 / yearHe/she is responsible for developing and executing Cabot's end-to-end process strategy, with the ultimate goal of driving GBS service efficiency across end-to-end processes (Record to Report R2R, Order to Cash O2C, Source to Pay S2C and Plan to Deliver P2D). This leader will define and lead the direction, governance, and operating model to deliver scalable, digitally-enabled business processes that improve performance, experience, and efficiency across the organization GBS and the rest of the enterprise.
Director Artificial Intelligence PMO Cabot CorpDirector Artificial Intelligence PMOBoston, MAThis policy, however, shall not apply to instances in which an employee who has access to the compensation information of other employees or applicants as part of that employee's essential job functions (such as in payroll or HR) discloses the compensation of such other employees or applicants to individuals who do not otherwise have access to such information, unless that disclosure is in response to a formal complaint or charge, in furtherance of an investigation, proceeding, hearing or other action, including an investigation conducted by Cabot, or otherwise as required by law. Our strength in research and development is a major reason why we have been an industry leader for more than 135 years in products such as reinforcing and specialty carbons, battery materials, aerogel, fumed metal oxides, inkjet colorants, masterbatches and conductive compounds.
Product Manager - Radium Services Illinois Tool Works IncProduct Manager - Radium ServicesBurlington, MA$100,000–$150,000 / year5+ years of experience in strategic marketing, product management, customer discovery, customer-driven innovation, application engineering, technical sales, radiochemistry, isotope production, nuclear materials processing, radiopharmaceuticals, or related technical industries. KEY RESPONSIBILITIES: Serve as the product management lead for QSA's radium services product line, including radium purification, irradiated material recycling, and target manufacturing for actinium-225 and lead-212 production.
High Complex CLIA LAB: Lab Director Nanobiosym IncHigh Complex CLIA LAB: Lab DirectorCambridge, MAThe Laboratory Director will provide clinical, scientific, and regulatory oversight to ensure Nanobiosym delivers accurate, reliable, and high-quality testing services in compliance with applicable regulatory and accreditation requirements, including CLIA, CAP, and other applicable state requirements. Qualified to serve as Clinical Laboratory Director of a high-complexity CLIA/CAP laboratory under applicable federal and Massachusetts state regulations -- Clinical Laboratory Director License issued by the Massachusetts Department of Public Health (MDPH) is required.
Senior Scientist or Principal Scientist, Targeted Proteomics Kymera TherapeuticsSenior Scientist or Principal Scientist, Targeted ProteomicsWatertown, MA$115,000–$215,000 / yearDomain leadership with cross-functional drug discovery : Highly organized, solutions-oriented scientist with the ability to manage multiple priorities simultaneously while driving innovation in targeted proteomics workflows and enabling program advancement through high-impact experimental data. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions.
Public Health Inspector- Registered Sanitarian Town of CohassetPublic Health Inspector- Registered SanitarianCohasset, MA$46.11–$47.97 / hourFood Establishment Inspections •Conduct routine, follow-up, complaint, and pre-operational inspections of all food establishments, trucks, farmers markets, residential and commercial kitchens in accordance with the Massachusetts State Sanitary Code (105 CMR 590.000). All offers of employment are conditional upon the satisfactory completion of a Criminal offense record inquiry ( CORI check, pre-employment DOT physical examination, drug test & all other background checks where required.
Manager, EHS Emergent BioSolutions IncManager, EHSCanton, MA$129,000–$156,000 / yearThis role partners cross-functionally with Site Leadership, Manufacturing, Quality, Engineering, and external agencies to enable compliant, efficient, and safe manufacturing operations while driving a proactive, risk-based safety culture aligned with cGMP expectations. Lead and execute comprehensive EH&S risk assessments (e.g., JSA, process hazard analysis, biosafety assessments) to identify and mitigate risks associated with biologics manufacturing, laboratories, utilities, and support functions.
Research Associate - Chemical and Biological Engineering Tufts UniversityResearch Associate - Chemical and Biological EngineeringMedford, MAThe Chemical and Biological Engineering department advances cutting-edge research across key areas including energy, catalysis, metabolic and cell engineering, nanomaterials, biomaterials, and environmental systems while fostering strong interdisciplinary collaboration across the university. Committed to innovation and societal impact, the department prepares graduates to solve complex global challenges, pursue lifelong learning, and emerge as leaders in chemical and biological engineering.
HSEQ Environmental Specialist III Hybrid- Andover MA Enel SpAHSEQ Environmental Specialist III Hybrid- Andover MAAndover, MA$123,000–$184,000 / yearResponsible for governance, oversight, and completion of specific environmental regulatory filings in one or more environmental programs including, but not limited to, solid and hazardous waste management, environmental management system (EMS), facility operational permits and compliance reporting, biodiversity, and environmental, social, and governance (ESG). Position requires communication and interaction with Enel business units that include but are not limited to operations, sustainability, strategy, government affairs, supply, legal, communications, auditing, and financial.
Director, Regulatory Affairs Liaison, Vaccines & Infectious Diseases Merck & Co IncDirector, Regulatory Affairs Liaison, Vaccines & Infectious DiseasesBoston, MA$210,400–$331,100 / yearRequired Skills: Biological Sciences, Biostatistics, Clinical Judgment, Clinical Trial Planning, Clinical Trials, Communication, Cross-Functional Collaboration, Detail-Oriented, Infectious Disease, Leadership, Medical Writing, Pharmaceutical Regulatory Affairs, Pharmacovigilance, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Intelligence, Regulatory Issues, Regulatory Strategy Development, Regulatory Writing. Primary activities include, but are not limited to: Functions with a high degree of independence and provides regulatory oversight for assigned products, functioning as the single, accountable, global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.
Senior Director, Supply Chain & Logistics X4 Pharmaceuticals IncSenior Director, Supply Chain & LogisticsBoston, MABuilding on its expertise in CXCR4 biology and the successful commercialization of XOLREMDI (mavorixafor), X4 is advancing a global Phase 3 clinical program evaluating mavorixafor for chronic neutropenia, a group of rare disorders characterized by persistently low neutrophil counts and an increased risk of serious infections. Plan and implement activities related to clinical and commercial supply chain, customs clearance, cost management, storage, warehousing, distribution, procurement, logistics, forecast, inventory control, data management, and production planning.