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57 Repligen Operations Jobs Hiring Near You

Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing ... operation to produce high-quality components. This role focuses on learning the injection molding ...

Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing ... operational efficiency, and safety compliance. This mid-level role serves as a technical leader in ...

Extrusion Associate I

Clifton, NY · On-site

$19 - $21/hr

Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing ... operations under supervision. Second shift Schedule: Monday - Friday 2:00pm-10:30pm Second shift ...

Extrusion Associate I

Clifton, NY · On-site

$19 - $21/hr

Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing ... operations under supervision. Second shift Schedule: Monday - Friday 2:00pm-10:30pm Second shift ...

The Global Environment, Health & Safety (EHS) Director provides strategic and operational ... Repligen Offers Our mission is to inspire advances in bioprocessing as a trusted partner in the ...

Position Summary Repligen is seeking a highly analytical and detail-oriented Commercial Operations Analyst focused on Incentive Compensation to support the design, administration, governance, and ...

Repligen is seeking a hands-on CNC Operator / Support Technician to support precision manufacturing ... This role combines CNC machine operation with post-machining fabrication and finishing, supporting ...

Showing results 21-40

RepliGen Jobs Information

Does Repligen pay people when they’re sick?

Yes. Most people get paid when they’re sick.
77% of people say they would get paid if they were sick but scheduled to work.
Based on data from 13 people who took the Breakroom Quiz between December 2024 and June 2026.

How easy is it to get time off at Repligen?

Most people find it easy to get time off.
92% of people report it’s easy to get time off.
Based on data from 12 people who took the Breakroom Quiz between December 2024 and May 2026.

How easy is it to take sick days at Repligen?

Most people find it easy to take sick days.
92% of people report that it’s easy to take time off if they are sick.
Based on data from 13 people who took the Breakroom Quiz between December 2024 and June 2026.

Do people at Repligen feel treated with respect by their managers?

Most people feel treated with respect by their managers.
82% of people say they’re treated with respect by their managers.
Based on data from 11 people who took the Breakroom Quiz between December 2024 and May 2026.

Do people at Repligen get to take their breaks without interruption?

Most people get breaks without interruption.
67% of people report that they get to take their breaks without interruption.
Based on data from 12 people who took the Breakroom Quiz between December 2024 and June 2026.

Is it stressful to work at Repligen?

Some people feel stressed out here.
64% of people say they often feel stressed out at work.
Based on data from 11 people who took the Breakroom Quiz between January 2025 and May 2026.

Do people at Repligen enjoy their jobs?

Most people enjoy their job.
70% of people report they enjoy their job.
Based on data from 10 people who took the Breakroom Quiz between January 2025 and May 2026.

Do people at Repligen recommend working with their team?

Only some people recommend working with their team.
46% of people report that they wouldn’t recommend working with their immediate team to a friend.
Based on data from 13 people who took the Breakroom Quiz between December 2024 and June 2026.

Do people get enough training when they start at Repligen?

Most people got enough training when they started.
67% of people report they got enough training when they started working here.
Based on data from 12 people who took the Breakroom Quiz between December 2024 and May 2026.

Do people get support to advance at Repligen?

Most people are given support to advance their career here.
In the last year, 73% of people report being given support to advance their career here.
Based on data from 11 people who took the Breakroom Quiz between December 2024 and May 2026.

Do workers feel well informed about how Repligen is doing?

Only some people feel well informed about how the company is doing.
50% of people feel that they aren’t kept well informed about how the company is doing as a whole.
Based on data from 10 people who took the Breakroom Quiz between January 2025 and May 2026.
What are the most popular job types at Repligen?
    What are the most popular categories at Repligen?
    Infographic showing various Operations job openings at Repligen in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 92% Physical, and 8% Hybrid job distribution.
    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

    Posted 7 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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