Textile & Biotech Manufacturing Technician

Anika Therapeutics; Bedford (MA); On-site; USD 32,000 - 41,000; Full time

Job summary

Anika Therapeutics in Bedford, MA is hiring a HYAFF Technician II to manufacture fiber and film-based textile products. You will follow SOPs and manufacturing directions, perform cutting and extrusion, and document all work per GMP guidelines.

The role requires 2–4 years in a cGMP setting, the ability to work flexible hours, and strong communication skills. PPE, safety protocols, and routine training are part of daily operations.

Qualifications

• High school diploma or GED or equivalent experience.
• 2–4 years of related experience in a cGMP manufacturing environment.
• Ability to work flexible hours to complete work activities.
• Strong written and verbal communication skills.
• Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas and wear PPE (gloves, safety glasses, etc).
• Ability to lift, pull, or push equipment up to 25–50 lbs and stand for up to 6 hours in a production suite.

Responsibilities

• Operates production equipment according to SOPs, Batch Records, MDs, and OPMs.
• Performs cutting, slitting, fiber and film extrusion, and/or packaging of textile woven and non-woven products.
• Performs scheduled cleaning and sterilization of equipment.
• Supports changeover activities.
• Troubleshoots and resolves process-related issues.
• Records data into Batch Records, log books, and OPMs.
• Reviews log books and forms.
• Documents all work activities according to Good Documentation Practices.
• Reports procedural deviations and nonconformance to management.
• Maintains current training on all assigned procedures, including read-and-understood, skills development, and classroom training activities.

Education

High school diploma or GED

Job description

Anika Therapeutics in Bedford, MA is hiring a HYAFF Technician II to manufacture fiber and film-based textile products. You will follow SOPs and manufacturing directions, perform cutting and extrusion, and document all work per GMP guidelines.

The role requires 2–4 years in a cGMP setting, the ability to work flexible hours, and strong communication skills. PPE, safety protocols, and routine training are part of daily operations.