Research Associate II, Quality Control
Ocular Therapeutix, Inc.
August 22, 2026
Remote friendly (Bedford, MA)
United States
Operations
Position Summary
As a Research Associate II, execute routine Quality Control (QC) testing activities as assigned. Support CAPAs, change controls, investigations, and deviations; participate in development and validation of analytical methods for the Analytical Development group. Assist with testing, project support, data review, ordering laboratory supplies, and laboratory upkeep.
Principal Duties and Responsibilities
- Support QC analytical chemistry testing using HPLC, UPLC, GC, KF, dissolution, and other instrumentation.
- Author technical reports as required.
- Ensure instrument calibration and qualification are up to date.
- Troubleshoot instrumentation issues and coordinate vendor repairs.
- Coordinate with Supervisor on scheduling testing for reagents and product samples.
- Participate in data review.
- Participate in method development and validation.
- Coordinate external outsourcing of testing.
- Support CAPAs, change controls, investigations, and deviations; ensure timely closure with Quality Assurance.
- Follow Good Documentation Practices (GDP) and maintain contemporaneous records/logbooks/forms.
- Adhere to cGMPs at all times.
Requirements
- Bachelor’s degree in Chemistry or related field.
- 2+ years of experience in a GMP Quality Control environment.
- Prior experience with HPLC and UPLC.
Preferred
- Knowledge of CFR 210, 211, USP, and FDA/ICH guidance.
- Experience with USP App IV dissolution apparatus.
Skills/Knowledge
- Knowledge of safe laboratory practices.
- Strong verbal and written communication.
Working Conditions
- Mix of office and laboratory environments; must be able to work in chemical laboratory environments.
As a Research Associate II, execute routine Quality Control (QC) testing activities as assigned. Support CAPAs, change controls, investigations, and deviations; participate in development and validation of analytical methods for the Analytical Development group. Assist with testing, project support, data review, ordering laboratory supplies, and laboratory upkeep.
Principal Duties and Responsibilities
- Support QC analytical chemistry testing using HPLC, UPLC, GC, KF, dissolution, and other instrumentation.
- Author technical reports as required.
- Ensure instrument calibration and qualification are up to date.
- Troubleshoot instrumentation issues and coordinate vendor repairs.
- Coordinate with Supervisor on scheduling testing for reagents and product samples.
- Participate in data review.
- Participate in method development and validation.
- Coordinate external outsourcing of testing.
- Support CAPAs, change controls, investigations, and deviations; ensure timely closure with Quality Assurance.
- Follow Good Documentation Practices (GDP) and maintain contemporaneous records/logbooks/forms.
- Adhere to cGMPs at all times.
Requirements
- Bachelor’s degree in Chemistry or related field.
- 2+ years of experience in a GMP Quality Control environment.
- Prior experience with HPLC and UPLC.
Preferred
- Knowledge of CFR 210, 211, USP, and FDA/ICH guidance.
- Experience with USP App IV dissolution apparatus.
Skills/Knowledge
- Knowledge of safe laboratory practices.
- Strong verbal and written communication.
Working Conditions
- Mix of office and laboratory environments; must be able to work in chemical laboratory environments.