Compliance Officer, US Biogen IdecCompliance Officer, USCambridge, MA$196,000–$270,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. By developing and delivering comprehensive training programs, you'll be an educational pillar for both new and established employees, fostering a culture of continuous learning and compliance awareness.
Program Manager, Investor & Internal Compliance WS DevelopmentProgram Manager, Investor & Internal ComplianceChestnut Hill, MACoordinate the annual internal controls testing program with our external audit partner, including scoping, evidence collection, remediation tracking, and risk ratings across financial reporting, cash management, lease compliance, and vendor management. Reporting to the Chief of Staff to the CFO, you will own a visible, high-trust function with direct exposure to senior executives, our institutional investor relationships, and the full compliance and controls landscape of a leading commercial real estate firm.
Compliance Specialist Astellas Pharma IncCompliance SpecialistWestborough, MAMay assist with the Internal Audit program for the organization, serving as an assistant auditor to help ensure all aspects of the GMP organization remain compliant with Astellas procedures and domestic / international GMP regulations. May assist senior QA staff in oversight of contract manufacturing organizations (CMO), monitoring information requests, reviewing CMO work, and following up on other compliance items.
Manager Customs & Compliance J.JillManager Customs & ComplianceQuincy, MassachusettsFull timeConfirms duty free eligibility of styles to be imported from Free Trade countries; consults with Sourcing regarding Free Trade strategies and monitors expiration dates associated with those programs. With competitive pay and benefits, a supportive culture, and the chance to make a real impact, this is more than a job, it’s an opportunity to bring our ethos keep it simple, make it matter to life in new and inspiring ways.
Senior Director, Quality Compliance Kiniksa PharmaceuticalSenior Director, Quality ComplianceLexington, MAThis role leads key quality systems including supplier oversight, product complaints, and inspection readiness, and partners cross-functionally to drive a proactive, risk-based quality culture that supports development through commercialization. We're seeking a Senior Director, Quality Compliance reporting to the VP, Head of Quality, who will be responsible for providing strategic leadership and oversight of the organization's global quality compliance programs, ensuring alignment with regulatory requirements and industry best practices.
NewClient Success Manager (Compliance) Resource InnovationsClient Success Manager (Compliance)Boston, MABalances multiple client priorities and facilitates collaboration across internal teams and external partners to drive successful program outcomes and continuous improvement. 3+ years of experience in client success, account management, project management, program management, consulting, or a related client-facing role.
Manager/Sr. Manager, US Compliance Zealand Pharma ASManager/Sr. Manager, US ComplianceCambridge, MA$105,000–$145,000 / yearReporting to the Head of US Compliance, you will help design policies, controls and training that do not yet exist, and prepare the frameworks that commercial, medical, market access and patient services colleagues will rely on once activities go live. Prepare launch readiness across the commercial model, assessing planned activities against the Anti-Kickback Statute, the False Claims Act, FDA advertising and promotion requirements, the PhRMA Code and OIG Compliance Program Guidance.
Compliance Specialist III - TPA/DPS NBT Bancorp IncCompliance Specialist III - TPA/DPSMA$71,160–$94,903 / yearContinue to learn and develop knowledge of more complex difficulty plans including cross-tested profit sharing allocations, balance forward valuations, and defined benefit and cash balance combo plans. At NBT we empower people to grow, innovate, and thrive through meaningful work, a supportive culture and opportunities to make a real impact in your community - because your success drives our success.
Lead Auditor, Quality Compliance Integra LifeSciences Holdings Corp.Lead Auditor, Quality ComplianceMansfield, MA$109,250–$149,500 / yearThe Lead Auditor, Quality Compliance will form part of the Corporate Audit team and will lead, coordinate and perform corporate audits of the Quality Management System (QMS) as part of Integra LifeScience's quality internal audit program across more than 15 design, manufacturing, and distribution facilities and a diverse portfolio of leading medical devices. The incumbent will possess extensive GMP audit experience and practical skills including: the ability to write objective technical audit reports, evaluate and make objective judgments on technical issues arising during the audit, utilize multi-cultural sensitivity while driving audits forward consistently and on time, as well as project and time management.
Permitting & Compliance Manager SparkChargePermitting & Compliance ManagerSomerville, MassachusettsThis role ensures that fuel storage, equipment operation, electrical work, and mobile charging infrastructure at each site meet all local, state, and federal requirements, while keeping permitting from becoming a bottleneck to go-live timelines. The Permitting & Compliance Manager owns the permitting, regulatory, and compliance pathway for every new SparkCharge site launch — from initial jurisdictional research through final permit approval and inspection sign-off.
NewProcurement Analyst Aequor Technologies LLCProcurement AnalystDevens, MAThe Site Procurement Analyst will maintain strong alignment with site and network strategies and initiatives while collaborating with stakeholders across Manufacturing, Supply Chain, Quality, Engineering, Finance, Facilities, Technical Services, and Global Category Management. This position will report to the Associate Director, Site Procurement Lead and serve as a key Procurement partner for the site, providing support across both Direct Materials and Indirect Procurement activities.
Associate Director or Director of Pharmacovigilance Operations Compass TherapeuticsAssociate Director or Director of Pharmacovigilance OperationsBoston, Massachusetts$175,000–$250,000 / yearManage scaling of PV operations, systems and processes, safety and vendor governance, risk management, internal and external partnerships, audit and inspection readiness, for commercial readiness in support of compliant regulatory filings and commercial launch; as detailed below. Establish and monitor rigorous metrics-based PV Key Performance Indicators (KPIs) to assess vendor performance, quality, regulatory compliance, timeliness, and data integrity ensuring high-quality case management, inspection readiness, and delivery of contracted services.
Tech Project Manager TechDigitalTech Project ManagerMA, MAExperience with pharma datasets like IQVIA, Veeva CRM, patient claims, or sales data, and working with cross-functional teams is essential. Oversee and tightly manage development, implementation, and maintenance of data platforms, integrations, and tools relevant to commercial data (e.g., sales data, patient claims, CRM data) as per plan.
Design Quality Engineer Katalyst Healthcares & Life SciencesDesign Quality EngineerAndover, MAAs a Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring endtoend design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world's most innovative companies unleash their potential.
Engineer IV/Complaint Analysts Takeda Pharmaceutical Co LtdEngineer IV/Complaint AnalystsLexington, MA$103,500–$162,690 / yearThe 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. What you bring to Takeda: Associates degree and 4+ years relevant experience or Bachelor's degree in Engineering, Chemistry, Biology, or related scientific/technical discipline with 2+ years relevant experience.
Information Systems Security Manager LeidosInformation Systems Security ManagerConcord, MassachusettsBachelor’s degree in an IT-related subject matter area from an accredited college or university and 12+ years of experience in an IT-related position with at least 10 years being in an operational cyber security-specific role (e.g., information system security manager, information system security officer, cyber security specialist) or have 15+ years of experience in an IT related position with at least 10 of those years in an operational cyber security specific role. Implement and manage the Risk Management Framework (RMF) Continuous Monitoring process by utilizing an automated ticketing system, ensuring accurate tracking, monitoring, and reporting of security controls, vulnerabilities, and remediation efforts within the organization's information systems.
Analyst II, Post Market Surveillance Abbott LaboratoriesAnalyst II, Post Market SurveillanceBurlington, MA$61,300–$122,700 / yearOne role is that of complaint investigation management which includes all activities pertaining to receiving and investigating reports of worldwide complaints/events on a variety of products; entering information into the complaint database; independently determining and filing appropriate medical devices reports with various regulatory agencies; participating on cross functional teams; and providing information on product complaints to various teams (e.g. disposable and implantable products, electronic and electro-mechanical medical devices and systems) such as performing non-destructive and destructive testing; reviewing of Device History Records; coordinating product testing/analysis with other SJM departments and external consultants; preparing technical reports of evaluation findings; operating and maintaining the Postmarket Surveillance Laboratory equipment.
Senior Analyst, Treasury & Portfolio Services Manulife Financial CorpSenior Analyst, Treasury & Portfolio ServicesBoston, MA$61,875–$103,125 / yearThe successful candidate will apply analytical thinking, technical accounting expertise, and industry knowledge to support strategic initiatives, evaluate complex transactions, resolve accounting and operational issues, and support critical service provider oversight activities. The Treasury & Portfolio Services (TPS) team is a specialized oversight and advisory function within Fund Administration that supports a diverse range of investment products through technical accounting expertise, operational governance, custody oversight, and analytical problem solving.
Sr. Program Finance Analyst The Charles Stark Draper Laboratory IncSr. Program Finance AnalystCambridge, MA$95,000–$245,000 / yearThis role will support their finance leadership, Program Managers, Control Account Managers (CAMs), and Schedulers to meet program objectives and provide accurate metrics on schedule and cost performance utilizing Earned Value or related program control principles. Draper supports many programs to improve work-life balance including workplace flexibility, employee clubs ranging from photography to yoga, health and finance workshops, off site social events and discounts to local museums and cultural activities.
Product Quality Engineer GTTProduct Quality EngineerMarlborough, MAOrganizational Relationships: Works with Divisional personnel and Costa Rica personnel including Product Quality Engineering (PQE), Post Market Quality Engineering (PMQE), and Post Market Analytics. This role will be responsible for reviewing each complaint record individually and identifying the appropriate risk lines and associated severities from the product's Risk Management File (RMF) that relate to what was reported by the complainant and the results of the investigation.