Quality Control Inspector I - 2nd Shift at Repligen

Ballston Lake, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

17 Apr, 26

Salary

23.0

Posted On

17 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Attention To Detail, Quality Assurance, Quality Control, Microsoft Office, Precision Measurement, Engineering Drawings, ISO Standards, Cleanroom Environment, Medical Device Manufacturing

Industry

Biotechnology Research

Description

Overview Are you detail-oriented, passionate about quality, and looking for a hands-on role in a fast-paced environment? Repligen’s Clifton Park facility is looking for a Quality Inspector I to join our 2nd shift team and play a vital role in ensuring our products meet the highest standards. 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! 2nd shift: 2:00pm-10:30pm, M-F Responsibilities What You’ll Do: Inspect products against acceptance criteria to maintain high-quality standards. Work closely with manufacturing teams to identify and resolve quality issues. Read and interpret engineering drawings, specifications, and purchase orders. Accurately document inspection results using Microsoft Office and other software. Use precision measurement tools like calipers and pin gauges. Operate in an ISO 7 cleanroom while following strict gowning procedures. Support additional quality-related functions as needed. Qualifications What You Bring: High School Diploma or equivalent (required); Bachelor’s degree in science or relevant experience preferred. Experience in Quality Assurance (QA) or Quality Control (QC) is a plus. Strong attention to detail and ability to work in a structured environment. Proficiency in basic math, measurements, and testing equipment. Experience in a cleanroom environment is highly desirable. Medical device or medical manufacturing experience is preferred. What Repligen Offers 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 $21/Hr.- $23/Hr. 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.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

Inspect products against acceptance criteria to maintain high-quality standards and work closely with manufacturing teams to identify and resolve quality issues. Document inspection results accurately and operate in an ISO 7 cleanroom while following strict gowning procedures.