Manufacturing Operator - hiring multiple positions!

Scorpion Therapeutics; Bedford (MA); On-site; USD 55,000 - 74,000; Full time

Job summary

Scorpion Therapeutics is seeking a Manufacturing Operator in Bedford, MA to perform formulation, inspection, in-process and finished product packaging under SOPs and supervisor direction.

The role requires 1+ year in a cGMP manufacturing environment and a high school diploma or equivalent, with an Associate degree or biotech certificate strongly preferred. On-site work Monday–Friday in a clean room setting.

Qualifications

• 1+ years related experience in a cGMP manufacturing environment.
• Clean room experience preferred.

Responsibilities

• Perform manufacturing processes including formulation, inspection, in-process packaging, and finished product packaging.
• Operate laboratory instruments (balances, pH meters, conductivity meters, mixers).
• Complete required manufacturing documentation (batch records, process routers, forms).
• Execute routine commercial/clinical production operations; apply GMP/GDP.
• Coordinate with Quality Control for testing, sample submission, and monitoring.

Skills

Manufacturing experience

Clean room experience

Laboratory instruments

Education

High school or equivalent

Associate degree or biotech cert

Tools

Balances

pH meters

Conductivity meters

Mixers

Job description

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