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Repligen Jobs (NOW HIRING)

Repligen

$126K - $193K/yr

Repligen is seeking a detail-oriented, hands-on, and strategic Senior Manager, Manufacturing to lead and oversee all production activities within our custom plastics fabrication shop. This includes ...

Repligen

Senior Manager, Manufacturing

Shrewsbury, MA

$126K - $193K/yr

Repligen is seeking a detail-oriented, hands-on, and strategic Senior Manager, Manufacturing to lead and oversee all production activities within our custom plastics fabrication shop. This includes ...

Repligen

$94K - $144K/yr

Make a global impact-join Repligen.We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No ...

Repligen

$150K - $186K/yr

Make a global impact-join Repligen.We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No ...

Repligen

Global Talent Management Manager

Waltham, MA

$130K - $160K/yr

Repligen is seeking a strategic and hands-on Manager, Global Talent Management, to help shape and elevate the employee experience across our global organization. This role partners closely with HR ...

Repligen

Senior Digital Marketing Specialist

Waltham, MA · Hybrid

$84K - $104K/yr

Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No ...

Repligen

$71K - $90K/yr

Make a global impact-join Repligen.We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No ...

Repligen

Consolidations Manager

Waltham, MA · On-site

$94K - $144K/yr

Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No ...

Repligen

Repligen is seeking an Associate Director, Digital Workplace to lead the delivery of seamless, secure, and productive technology experience for Repligen employees globally. This role provides ...

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How much do repligen jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for repligen in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What does the company Repligen do?

Repligen is a biotechnology company that develops and manufactures bioprocessing technologies and products used in the production of biologics and pharmaceuticals. Employees in related roles often work with bioprocessing equipment, chromatography systems, and biomanufacturing processes to support drug development and production.

Is Repligen a legitimate company?

Repligen is a publicly traded biotechnology company specializing in bioprocessing technologies and solutions. It is a well-established firm with a verified corporate presence, making it a legitimate organization for employment or business purposes.

What types of teams and departments do Repligen employees typically collaborate with during a project?

At Repligen, professionals often work in cross-functional teams that include colleagues from R&D, manufacturing, quality assurance, regulatory, and sales. Effective collaboration is key, as projects usually involve input from scientists, engineers, and commercial staff to ensure products meet both technical and client requirements. This environment fosters strong communication skills and offers opportunities to learn from diverse experts, which can be valuable for both personal and career development.

What are the key skills and qualifications needed to thrive as a bioprocessing professional at Repligen, and why are they important?

To thrive as a bioprocessing professional at Repligen, you need a solid background in biotechnology, biochemistry, or a related field, often supported by a relevant degree and experience in bioprocessing or manufacturing. Familiarity with bioprocessing equipment, chromatography systems, and quality control standards like GMP is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are essential soft skills for success in this role. These competencies ensure efficient production, product quality, and compliance with industry regulations in a dynamic life sciences environment.

What does a Repligen employee do?

Employees at Repligen typically work in the biotechnology and life sciences sector, focusing on developing and manufacturing products that support bioprocessing and biomanufacturing. Job roles can range from research and development, manufacturing, quality assurance, and technical support to sales and marketing. Their work often involves producing proteins, filtration systems, and other products used in the creation of biopharmaceuticals. Repligen employees collaborate to ensure product quality, regulatory compliance, and innovation in bioprocessing solutions. The company is known for its contributions to advancing biologic drug manufacturing through its products and technologies.

What is the difference between Repligen vs Process Development Scientist?

AspectRepligenProcess Development Scientist
Required CredentialsBachelor's or Master's in biotech, chemical engineering, or related fieldsBachelor's or Master's in biotech, chemical engineering, or related fields
Work EnvironmentBiotech manufacturing and R&D facilitiesBiotech or pharmaceutical R&D and manufacturing labs
Employer & Industry UsageBiotech companies, specializing in bioprocessing solutionsBiotech and pharmaceutical companies involved in process development
Common Search & ComparisonRepligen vs Process Development Scientist

Repligen is a biotech company focusing on bioprocessing solutions, while a Process Development Scientist works within biotech or pharma companies to develop and optimize manufacturing processes. Both roles require similar educational backgrounds and work in related environments, but Repligen is a specific employer, whereas Process Development Scientist is a job title across multiple organizations.

What is a Repligen job?

A Repligen job typically refers to a position at Repligen Corporation, a company specializing in bioprocessing technologies used in the production of biologic drugs. Jobs at Repligen span various functions, including research and development, manufacturing, quality control, sales, and engineering. Employees contribute to advancing bioprocessing solutions that support industries like pharmaceuticals and biotechnology. Working at Repligen often involves collaborating on innovative technologies that improve drug development processes.

How much do you get paid at Repligen?

Salaries at Repligen vary depending on the role, experience, and location. Entry-level positions typically start around $50,000 annually, while more experienced roles can earn over $100,000. Compensation may also include benefits such as health insurance and bonuses.

Is Repligen a good company to work for?

Repligen is a biotechnology company that offers roles in bioprocessing, manufacturing, and research. Employees generally report a collaborative work environment, competitive benefits, and opportunities for professional growth, especially for those with technical skills and relevant certifications. As with any company, experiences can vary based on role and location.
More about Repligen jobs
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Repligen jobs near you
Infographic showing various Repligen job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 87% Physical, and 13% Hybrid job distribution, with an average salary of $54,791 per year, or $26.3 per hour.
Quality Assurance Document Control Associate II

Quality Assurance Document Control Associate II

Repligen

Clifton Park, NY

$22.53 - $29/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Repligen rating

7.6

Company rating: 7.6 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

Job description

Make a global impact-join Repligen.
We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No matter your role or background, at Repligen, you will play a key part in shaping some of the most innovative and life-changing therapies in the world. We foster a culture of purpose, collaboration, and shared success-where every voice matters and every contribution drives progress. Join us!
The Quality Assurance Document Control Associate is responsible for the administration, maintenance, and control of Quality Management System (QMS) documentation in accordance with the requirements of ISO 9001:2015. This role ensures that documented information is properly reviewed, approved, distributed, and maintained to support regulatory compliance, operational efficiency, and document integrity across the organization.
The position supports document lifecycle management including creation, revision, archival, and retrieval of controlled documents such as Standard Operating Procedures (SOPs), work instructions, forms, policies, specifications, and records.
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.

Key Responsibilities:

Document Control Management

  • Maintain and administer the document control system for the Quality Management System.
  • Ensure controlled documents are reviewed, approved, issued, and revised in accordance with established procedures.
  • Manage document numbering, formatting, version control, and change history.
  • Ensure obsolete documents are promptly removed from use and archived appropriately.
  • Maintain document retention and archival processes in accordance with company policies.
  • Issue product batch records and finished product labels.

QMS Documentation Support

  • Coordinate the creation and revision of SOPs, forms, policies, and quality records.
  • Ensure documentation meets internal standards for formatting, clarity, and compliance.
  • Maintain the master list or document register for all controlled documents.
  • Support cross-functional teams with document updates and change requests.

Compliance and Audit Support

  • Ensure documented information complies with QMS requirements and applicable regulatory standards.
  • Provide document control support during internal, customer, and third-party audits.
  • Retrieve and provide documentation and records requested during audits or inspections.
  • Assist with periodic reviews of QMS documentation to ensure accuracy and effectiveness.

Training and Distribution

  • Distribute controlled documents to appropriate personnel and departments.
  • Coordinate training assignments when new or revised documents are released.
  • Ensure employees have access to current versions of required documentation.

Continual Improvement

  • Identify opportunities to improve document control processes and workflows.
  • Participate in quality improvement initiatives and QMS projects.

Qualifications:

  • Minimum of 2 years of experience in quality, preferably in an ISO 9001:2015-certified environment.
  • Strong knowledge of QMS principles, auditing, and process improvement methodologies.
  • Proficiency in using quality management software and Microsoft Office Suite.
  • Excellent communication, organizational, and analytical skills.
  • Certification in ISO 9001:2015 auditing (e.g., Lead Auditor or Internal Auditor) is a plus.

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 hourly rate for this role, based in the United States of America is $22.53 - 29.00. 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.

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