Manufacturing Operator - hiring multiple positions!
Ocular Therapeutix, Inc.
August 22, 2026
On-site
Bedford, MA
Operations
Position Summary
The Manufacturing Operator performs manufacturing processes related to Ocular Therapeutix products by following SOPs and supervisor direction in accordance with current GMP and company procedures. Full-time, onsite Monday–Friday in Bedford, MA.
Principal Duties and Responsibilities
- Perform manufacturing processes (formulation, inspection, in-process packaging, finished product packaging) including calculating requirements, weighing materials, and operating equipment per documented SOPs.
- Operate laboratory instruments (e.g., balances, pH meters, conductivity meters, mixers).
- Complete required manufacturing documentation (batch records, process routers, forms).
- Execute routine commercial/clinical production operations; apply GMP/GDP.
- Work in an environmentally controlled area (ECA) as required.
- Maintain cleanliness and organization; manage gowning, process, and stocking areas.
- Troubleshoot minor equipment and/or process issues.
- Work safely; notify management of safety issues/risks.
- Report procedural deviations and nonconformance.
- Coordinate with cross-functional teams (including Quality Control) for testing, sample submission, and monitoring.
- Maintain training for assigned procedures.
Requirements
- High school education or equivalent required; Associate degree or biotechnology certificate strongly preferred.
- 1+ years related experience in a cGMP manufacturing environment.
- Clean room experience preferred.
Working Conditions
- Gowning and PPE required (safety glasses/goggles, gloves, safety shoes).
- Lift/push/pull up to 25–50 lbs; stand up to 6 hours; climb ladders/work platforms.
- Flexible hours; work around chemicals (alcohols, acids, bases).
Salary Range
$55,000 USD - $74,000 USD
The Manufacturing Operator performs manufacturing processes related to Ocular Therapeutix products by following SOPs and supervisor direction in accordance with current GMP and company procedures. Full-time, onsite Monday–Friday in Bedford, MA.
Principal Duties and Responsibilities
- Perform manufacturing processes (formulation, inspection, in-process packaging, finished product packaging) including calculating requirements, weighing materials, and operating equipment per documented SOPs.
- Operate laboratory instruments (e.g., balances, pH meters, conductivity meters, mixers).
- Complete required manufacturing documentation (batch records, process routers, forms).
- Execute routine commercial/clinical production operations; apply GMP/GDP.
- Work in an environmentally controlled area (ECA) as required.
- Maintain cleanliness and organization; manage gowning, process, and stocking areas.
- Troubleshoot minor equipment and/or process issues.
- Work safely; notify management of safety issues/risks.
- Report procedural deviations and nonconformance.
- Coordinate with cross-functional teams (including Quality Control) for testing, sample submission, and monitoring.
- Maintain training for assigned procedures.
Requirements
- High school education or equivalent required; Associate degree or biotechnology certificate strongly preferred.
- 1+ years related experience in a cGMP manufacturing environment.
- Clean room experience preferred.
Working Conditions
- Gowning and PPE required (safety glasses/goggles, gloves, safety shoes).
- Lift/push/pull up to 25–50 lbs; stand up to 6 hours; climb ladders/work platforms.
- Flexible hours; work around chemicals (alcohols, acids, bases).
Salary Range
$55,000 USD - $74,000 USD