Repligen Corporation

Quality Engineer II

Repligen Corporation$85K — $115K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Biological Science, Engineering, Physical Science, or related discipline.
  • 5+ years of experience in Quality Engineering within an ISO 9001 or equivalent regulated environment.
  • Experience in New Product Development Quality Engineering, particularly in biotech.
  • Knowledge of cell culture, filtration, and chromatography in bioprocessing.
  • ASQ Certified Quality Engineer (CQE), CRE, or equivalent preferred.
  • Internal auditing experience is beneficial.
  • Strong communication skills for effective collaboration across functions.

Responsibilities

  • Apply validation principles and design control processes to ensure product quality.
  • Support New Product Introduction (NPI) and maintain Design History Files for product releases.
  • Guide Design Controls and Risk Management activities in collaboration with engineering and manufacturing.
  • Conduct risk management activities and ensure products meet quality expectations.
  • Develop and improve testing methods for product performance evaluation.
  • Review equipment documentation for commercial manufacturing operations.
  • Manage priorities while maintaining attention to detail and execution focus.

Benefits

  • Paid time off for work-life balance.
  • Health, dental, and vision insurance coverage.
  • Retirement benefits to support future planning.
  • Flexible spending accounts for healthcare and dependent care expenses.
  • Potential participation in variable cash programs such as bonuses or commissions.
Full Job Description
We are seeking an experienced Quality Engineer II to support quality excellence across new product development, manufacturing transfer, and commercial operations. In this role, you will serve as a trusted quality partner, working cross-functionally to ensure products are developed and manufactured in accordance with quality, regulatory, and customer expectations.

You will play an important role in risk management, design controls, validation, and continuous improvement initiatives, helping teams make informed decisions that support successful product launches and reliable manufacturing performance. The ideal candidate is a proactive problem solver who thrives in a collaborative environment, takes ownership of outcomes, and is passionate about driving quality throughout the product lifecycle.

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.
  • Apply Validation Principles and Design Control processes in accordance with applicable regulatory and industry requirements (including ISO standards, ASME BPE, CE, BPOG, REACH, and others), ensuring product and process quality throughout development and commercialization.
  • Support the New Product Introduction (NPI) team through the deployment of Quality Engineering tools that enable the effective development, transfer, and lifecycle management of products and processes. Partner closely with cross-functional teams to verify development deliverables and maintain Design History Files that support successful product release.
  • Provide guidance and support in Design Controls and Risk Management activities for new product development and design change projects. Collaborate with Engineering, Manufacturing, and Product Development teams to proactively identify risks and drive quality-focused decision making.
  • Support the completion of Risk Management activities (FMEA), Design Verification, and Process Verification efforts to ensure products and processes consistently meet quality and performance expectations.
  • Assist in the development, validation, and continuous improvement of test methods that effectively evaluate product and process performance.
  • Review Equipment IQ/OQ/PQ documentation in support of commercial manufacturing operations.
  • Demonstrate strong organizational skills and the ability to effectively manage multiple priorities while maintaining attention to detail and a focus on execution.
  • Bring a self-directed approach, exercising sound judgment, accountability, and problem-solving skills to support quality objectives and business needs.
  • Participate in customer complaint investigations, partnering with stakeholders to identify root causes and implement sustainable corrective actions.
  • Execute change controls and facilitate Change Control Review Board activities, ensuring effective communication, alignment, and timely decision making across impacted teams.
  • Review and approve nonconformances, deviations, failure investigations, and corrective action plans, helping ensure robust solutions are implemented and sustained.
  • Utilize Lean and Six Sigma methodologies to identify opportunities, improve processes, reduce risk, and support a culture of continuous improvement.
Qualifications
  • Bachelor's degree in Biological Science, Engineering, Physical Science, or a related discipline.
  • Demonstrated experience in New Product Development Quality Engineering.
  • Experience supporting biotech hardware, consumable products, and associated manufacturing processes.
  • Working knowledge of cell culture, filtration, and chromatography operations within a bioprocessing environment.
  • ASQ Certified Quality Engineer (CQE), CRE, or equivalent certification preferred.
  • Minimum of 5 years of Quality Engineering experience within an ISO 9001 Quality Management System or equivalent regulated environment.
  • Internal auditing experience.
  • Strong communication and relationship-building skills, with the ability to effectively collaborate across technical and operational functions.
  • Ability to influence outcomes, navigate complex challenges, and contribute to informed, risk-based decision making.
  • Proven ability to drive results, manage competing priorities, and support continuous improvement initiatives in a fast-paced environment.


The estimated base salary range for this role, based in the United States of America is $85,000-$115,000. 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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