Manufacturing Associate

Scorpion Therapeutics; Worcester (MA); On-site; USD 54,000 - 76,000; Full time

Job summary

Scorpion Therapeutics is seeking a detail-oriented Manufacturing Associate to perform GMP-compliant manufacturing, assembly, labeling, packaging and inspections in a cleanroom environment.

You will follow SOPs, batch records and production schedules, maintain accurate GDP/GMP documentation, assist with material handling, and participate in quality checks and changeovers while collaborating with Quality, Engineering and Supply Chain teams.

Qualifications

• GMP knowledge and following quality system requirements.
• Accurate documentation and attention to detail.
• Organization and time management with basic computer skills.

Responsibilities

• Perform manufacturing, assembly, labeling, packaging, and inspection operations in a GMP environment.
• Follow approved SOPs, batch records, work instructions, and production schedules.
• Complete GMP documentation accurately and contemporaneously (GDP).
• Assist with material handling: staging, issuing, and reconciliation of in-process materials and finished goods.
• Conduct in-process inspections and quality checks.
• Maintain cleanroom/production areas per GMP and company policies.
• Perform line clearances, room setup, and product/room changeovers as required.
• Identify and report quality, safety, equipment, or process issues.
• Support investigations, deviations, corrective actions, and continuous improvement.
• Participate in equipment cleaning and routine maintenance.
• Comply with safety policies, GMP regulations, and training requirements.
• Collaborate with Quality, Engineering, Supply Chain, and other departments.

Skills

GMP knowledge

Documentation accuracy

Attention to detail

MS Office

Team collaboration

Education

High School Diploma or GED

Associate degree/technical certification

Job description

Responsibilities

• Perform manufacturing, assembly, labeling, packaging, and inspection operations in a GMP environment.
• Follow approved SOPs, batch records, work instructions, and production schedules.
• Complete GMP documentation accurately and contemporaneously (GDP).
• Assist with material handling: staging, issuing, and reconciliation of in-process materials and finished goods.
• Conduct in-process inspections and quality checks.
• Maintain cleanroom/production areas per GMP and company policies.
• Perform line clearances, room setup, and product/room changeovers as required.
• Identify and report quality, safety, equipment, or process issues.
• Support investigations, deviations, corrective actions, and continuous improvement.
• Participate in equipment cleaning and routine maintenance.
• Comply with safety policies, GMP regulations, and training requirements.
• Collaborate with Quality, Engineering, Supply Chain, and other departments.

Required Skills/Knowledge

• Basic understanding of GMP and quality system requirements; follow detailed written procedures.
• Strong attention to detail; accurate documentation.
• Organizational/time management skills; basic computer proficiency (Microsoft Office).
• Ability to work independently and in a team; effective verbal/written communication.
• Willingness to learn new processes/technologies.
• Lift up to 25 lbs; wear PPE (including cleanroom gowning).
• Ability to stand/walk/bend/reach and perform repetitive motions for extended periods.
• Position requires an eye exam.

Experience

• 0–2 years manufacturing preferred.
• Medical device/pharma/biotech/combination product manufacturing preferred/plus.
• Regulated environment experience preferred.

Education

• High School Diploma or GED required.
• Associate degree/technical certification/coursework in related field preferred.

Salary Range

• $54,000 USD - $76,000 USD