Regulatory Compliance Specialist Jobs in Massachusetts
Regulatory Compliance Specialist jobs in Massachusetts are among the most active in the country, concentrated in life sciences, financial services, and healthcare, with openings from entry-level analysts through senior program managers. Boston, Cambridge, and Worcester anchor most of the hiring, driven by employers like Biogen, Fidelity Investments, and Mass General Brigham, all of which maintain large, established compliance functions. Regulatory affairs for biotech and pharma, financial regulatory compliance under state and federal oversight, and healthcare compliance are the most in-demand specialties. Find a role that fits below and apply directly.
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Showing 5 of 17+ Regulatory Compliance Specialist jobs
This role is expected to model our Leadership Behaviors—Integrity & Compliance, Customer Focus, Collaboration, Courage, Team Empowerment, and Accountability & Results—in all aspects of work.
Responsibilities
- Understand legal requirements related to Repligen's products and services and ensure compliance with applicable industry regulations while serving as a trusted resource for regulatory and product compliance matters.
- Maintain the latest versions and subscriptions of standards applicable to products, services (USP, EP, EDQM, JP, among others), and systems implemented within the company, ensuring the organization remains aligned with evolving industry requirements.
- Continuously build and maintain expertise in EMC, Low Voltage Directive, Machine Directive, Pressure Equipment Directive, and other emerging regulatory requirements that may impact Repligen's products, services, customers, and business operations.
- Read and interpret regulatory requirements and customer technical specifications, assess applicability, and implement effective compliance processes that support business objectives and customer expectations.
- Partner cross-functionally with QC, Engineering, EH&S, Support, Applications, Organizational Knowledge, and Sourcing teams to identify compliance gaps, provide recommendations, and drive effective solutions.
- Apply and support corporate guidelines within the business unit, promoting consistency, accountability, and compliance across products and processes.
- Maintain accurate, organized, and up-to-date compliance documentation for raw materials and products, including RoHS certifications, REACH declarations, Safety Data Sheets (SDS), and related regulatory records to support customer and business needs.
- Support customer compliance requests by gathering technical information, providing documentation, and delivering timely, high-quality responses that strengthen customer confidence and trust.
- Coordinate external testing, certification, and compliance activities with third-party organizations and laboratories, ensuring effective project execution, communication, and follow-through.
- Monitor and support compliance efforts related to EMC, REACH, RoHS, PFAS, Pressure Equipment Directive (PED), and other applicable global regulations, proactively identifying risks and helping drive resolution.
- Review, modify, and approve Quality Agreements and User Requirement Specifications (URS), ensuring alignment with regulatory requirements and company standards.
- Work closely with Organizational Knowledge and other stakeholders to provide guidance aligned with corporate policies regarding trademarks, registered marks, and related compliance considerations.
- Participate in product design and development activities, providing compliance guidance early in the product lifecycle and partnering with technical teams to support informed decision-making.
- Help investigate compliance-related issues, support root cause analysis efforts, and collaborate with internal and external stakeholders to implement corrective actions when needed.
- Develop, maintain, and continuously improve legal and regulatory requirements matrices for EH&S and product compliance programs, supporting long-term compliance readiness and operational excellence.
Education & Qualifications
- Bachelor's degree in Engineering, Regulatory Affairs, Life Sciences, Chemistry, Physics, or a related technical discipline required.
- Minimum 5 years of experience in regulatory compliance, product compliance, quality systems, or a related field.
- Experience within life sciences, biopharmaceutical, medical device, diagnostics, analytical instrumentation, or other highly regulated industries preferred.
- Working knowledge of global product compliance and regulatory requirements such as EMC, PED, RoHS, REACH, PFAS, Cal Prop 65, Low Voltage Directive, Machine Directive, or similar standards.
- Experience interpreting technical regulations, customer requirements, and industry standards and translating them into business processes and compliance actions.
- Familiarity with 21 CFR Part 11, Annex 11, USP, EP, EDQM, JP, or comparable pharmaceutical and life sciences standards preferred.
- Experience coordinating external testing, certification, validation, or regulatory assessment activities is highly desirable.
- Strong analytical, problem-solving, and organizational skills with exceptional attention to detail.
- Experience working with ERP systems such as SAP and document management platforms, including SharePoint.
- Proven ability to build strong partnerships and effectively influence cross-functional stakeholders.
- Excellent written and verbal communication skills.
- Demonstrated ability to manage multiple priorities, adapt to changing requirements, and drive results in a fast-paced, growth-oriented environment.
Our mission is to inspire advances in bioprocessing as a trusted partner in the production of biologic drugs that improve human health worldwide. Focused on cost and process efficiencies, we deliver innovative technologies and solutions that help set new standards in bioprocessing. The estimated base salary range for this role, based in the United States of America is $85,000-$125,000. Compensation decisions are dependent on several factors including, but not limited to an individual's ,qualifications, location, internal equity, and alignment with market data. Additionally, employees are eligible to participate in one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits such as paid time off, health/dental/vision, retirement benefits and flexible spending accounts. All compensation and benefits information will be confirmed in writing at the time of offer.
This role is expected to model our Leadership Behaviors—Integrity & Compliance, Customer Focus, Collaboration, Courage, Team Empowerment, and Accountability & Results—in all aspects of work.
Responsibilities
- Understand legal requirements related to Repligen's products and services and ensure compliance with applicable industry regulations while serving as a trusted resource for regulatory and product compliance matters.
- Maintain the latest versions and subscriptions of standards applicable to products, services (USP, EP, EDQM, JP, among others), and systems implemented within the company, ensuring the organization remains aligned with evolving industry requirements.
- Continuously build and maintain expertise in EMC, Low Voltage Directive, Machine Directive, Pressure Equipment Directive, and other emerging regulatory requirements that may impact Repligen's products, services, customers, and business operations.
- Read and interpret regulatory requirements and customer technical specifications, assess applicability, and implement effective compliance processes that support business objectives and customer expectations.
- Partner cross-functionally with QC, Engineering, EH&S, Support, Applications, Organizational Knowledge, and Sourcing teams to identify compliance gaps, provide recommendations, and drive effective solutions.
- Apply and support corporate guidelines within the business unit, promoting consistency, accountability, and compliance across products and processes.
- Maintain accurate, organized, and up-to-date compliance documentation for raw materials and products, including RoHS certifications, REACH declarations, Safety Data Sheets (SDS), and related regulatory records to support customer and business needs.
- Support customer compliance requests by gathering technical information, providing documentation, and delivering timely, high-quality responses that strengthen customer confidence and trust.
- Coordinate external testing, certification, and compliance activities with third-party organizations and laboratories, ensuring effective project execution, communication, and follow-through.
- Monitor and support compliance efforts related to EMC, REACH, RoHS, PFAS, Pressure Equipment Directive (PED), and other applicable global regulations, proactively identifying risks and helping drive resolution.
- Review, modify, and approve Quality Agreements and User Requirement Specifications (URS), ensuring alignment with regulatory requirements and company standards.
- Work closely with Organizational Knowledge and other stakeholders to provide guidance aligned with corporate policies regarding trademarks, registered marks, and related compliance considerations.
- Participate in product design and development activities, providing compliance guidance early in the product lifecycle and partnering with technical teams to support informed decision-making.
- Help investigate compliance-related issues, support root cause analysis efforts, and collaborate with internal and external stakeholders to implement corrective actions when needed.
- Develop, maintain, and continuously improve legal and regulatory requirements matrices for EH&S and product compliance programs, supporting long-term compliance readiness and operational excellence.
Education & Qualifications
- Bachelor's degree in Engineering, Regulatory Affairs, Life Sciences, Chemistry, Physics, or a related technical discipline required.
- Minimum 5 years of experience in regulatory compliance, product compliance, quality systems, or a related field.
- Experience within life sciences, biopharmaceutical, medical device, diagnostics, analytical instrumentation, or other highly regulated industries preferred.
- Working knowledge of global product compliance and regulatory requirements such as EMC, PED, RoHS, REACH, PFAS, Cal Prop 65, Low Voltage Directive, Machine Directive, or similar standards.
- Experience interpreting technical regulations, customer requirements, and industry standards and translating them into business processes and compliance actions.
- Familiarity with 21 CFR Part 11, Annex 11, USP, EP, EDQM, JP, or comparable pharmaceutical and life sciences standards preferred.
- Experience coordinating external testing, certification, validation, or regulatory assessment activities is highly desirable.
- Strong analytical, problem-solving, and organizational skills with exceptional attention to detail.
- Experience working with ERP systems such as SAP and document management platforms, including SharePoint.
- Proven ability to build strong partnerships and effectively influence cross-functional stakeholders.
- Excellent written and verbal communication skills.
- Demonstrated ability to manage multiple priorities, adapt to changing requirements, and drive results in a fast-paced, growth-oriented environment.
Our mission is to inspire advances in bioprocessing as a trusted partner in the production of biologic drugs that improve human health worldwide. Focused on cost and process efficiencies, we deliver innovative technologies and solutions that help set new standards in bioprocessing. The estimated base salary range for this role, based in the United States of America is $85,000-$125,000. Compensation decisions are dependent on several factors including, but not limited to an individual's ,qualifications, location, internal equity, and alignment with market data. Additionally, employees are eligible to participate in one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits such as paid time off, health/dental/vision, retirement benefits and flexible spending accounts. All compensation and benefits information will be confirmed in writing at the time of offer.
See All 17 Regulatory Compliance Specialist Jobs in Massachusetts
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Find JobsRegulatory Compliance Specialist Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
Regulatory Compliance Specialist Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
What Massachusetts Employers Look For
The qualifications that appear most often in regulatory compliance specialist jobs across Massachusetts.
- Bachelor's degree in a related field such as life sciences, business, or law
- Demonstrated knowledge of FDA, SEC, or state regulatory frameworks relevant to Massachusetts industries
- Professional certification such as CCEP, CRCM, or RAC preferred by most Massachusetts employers
- Experience interpreting and applying federal and Massachusetts state regulations in a professional setting
- Strong written communication skills for policy documentation, audits, and regulatory submissions
- Proficiency with compliance management software and document control systems used in regulated industries
Regulatory Compliance Specialist Jobs in Massachusetts: Frequently Asked Questions
How do you become a regulatory compliance specialist in Massachusetts?
Most Massachusetts employers expect a bachelor's degree in a relevant field such as life sciences, public health, finance, or business, paired with direct experience in a regulated industry. Massachusetts does not require a single state-issued license for this role, but credentials like the Certified Compliance and Ethics Professional designation or the Regulatory Affairs Certification strengthen your candidacy considerably. Candidates entering biotech or pharma often build toward roles through quality assurance or regulatory affairs associate positions at Massachusetts life sciences companies.
How much do regulatory compliance specialists make in Massachusetts?
Regulatory compliance specialists in Massachusetts earn a median of about $102,060 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $63,340 for the lowest 10% to over $161,920 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire regulatory compliance specialists in Massachusetts?
Employers hiring regulatory compliance specialists in Massachusetts right now include Signature Healthcare, CAI, and Telus, based on current listings on Migrate Mate as of September 2026. Massachusetts's dense concentration of biotech, financial services, and academic medical centers means compliance hiring stays active even outside peak recruiting seasons.
Which Massachusetts cities have the most regulatory compliance specialist jobs?
Boston, Brockton, and Massachusetts have the most regulatory compliance specialist openings in Massachusetts. Boston and Cambridge dominate because they house the headquarters and regional offices of major life sciences companies, financial institutions, and academic medical centers, while Worcester draws compliance hiring from its growing healthcare and biotech corridor anchored by UMass Memorial Health and a cluster of medical device firms.
Are there remote regulatory compliance specialist jobs in Massachusetts?
Yes, and more than most fields. About 75% of regulatory compliance specialist openings tied to Massachusetts are remote or hybrid as of September 2026, reflecting that much of the work involves policy review, documentation, and audit preparation rather than on-site inspection. Roles in financial regulatory compliance and privacy compliance tend to offer the most remote flexibility, while positions requiring lab or facility audits are typically on-site.
How can I get hired as a regulatory compliance specialist in Massachusetts with little or no experience?
The most realistic entry path is through a quality assurance associate, regulatory affairs coordinator, or compliance analyst role at a Massachusetts life sciences or healthcare organization, where you handle documentation and audit support under senior oversight. Large employers like Boston Scientific and Dana-Farber Cancer Institute run structured associate or rotational programs that onboard candidates without direct compliance experience. Pursuing a RAC credential or completing a graduate certificate in regulatory affairs from a Massachusetts institution such as Northeastern University gives candidates a measurable edge when applying to entry-level openings.
Where can I find and apply to regulatory compliance specialist jobs in Massachusetts?
You can find and apply to regulatory compliance specialist jobs in Massachusetts on Migrate Mate, which lists current Massachusetts openings across life sciences, healthcare, financial services, and other regulated industries. Find roles that fit your background and apply directly to the ones that match.
See All 17 Regulatory Compliance Specialist Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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