Repligen Corporation

Regulatory Compliance Engineer II

Repligen Corporation$85K — $125K *
US-AnywhereRemote in Massachusetts, US
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

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 in life sciences, biopharmaceutical, medical device, diagnostics, or analytical instrumentation preferred.
  • Working knowledge of global compliance standards like EMC, PED, RoHS, REACH, and PFAS.
  • Familiarity with 21 CFR Part 11 and other relevant pharmaceutical standards.
  • Proven ability to influence cross-functional teams effectively.
  • Strong analytical and organizational skills with attention to detail.

Responsibilities

  • Understand legal requirements for products and ensure regulatory compliance.
  • Maintain updated standards for compliance and services across the organization.
  • Build expertise in significant regulatory directives impacting products and operations.
  • Assess regulatory requirements and implement compliance processes aligned with business objectives.
  • Collaborate cross-functionally to identify compliance gaps and solutions.
  • Support customer compliance needs with technical information and documentation.
  • Coordinate external testing and compliance activities for effective project management.

Benefits

  • Paid time off for work-life balance.
  • Comprehensive health, dental, and vision coverage.
  • Retirement benefits to plan for the future.
  • Flexible spending accounts for tax savings on healthcare and dependent care expenses.
Full Job Description
Repligen is seeking a Regulatory Compliance Engineer to support product compliance activities across our Hardware, Automation, Chromatography, and Protein business units. In this highly collaborative role, you will help ensure our products meet global regulatory, environmental, and customer compliance requirements while partnering with engineering, quality, sourcing, and R&D teams to address complex compliance challenges. This is an excellent opportunity to contribute to innovative technologies, support a growing global organization, and play a key role in bringing compliant products to market.

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.


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.

About Repligen Corporation

Repligen Corporation is a bioprocessing company headquartered in Waltham, Massachusetts that provides products and services to the biopharmaceutical industry. The company's products are used in the production of monoclonal antibodies, recombinant proteins, and vaccines. Repligen's product portfolio includes chromatography products, filtration products, and protein A ligands. The company also provides bioprocess services, including process development and optimization, analytical testing, and protein characterization. Repligen was founded in 1981 and has grown through a combination of organic growth and acquisitions.
Learn more about Repligen Corporation
Size
1,852 employees
Market Cap
$9.5 billion
Industry
Net Income
$59.9 million
5 Year Trend
+45%
Revenue
$366.2 million
NASDAQ

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