Aseptic Manufacturing Tech – 2nd Shift, Flexible Hours

Anika Therapeutics

Bedford (MA)

On-site

USD 39,000 - 48,000

Full time

38 hours ago
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Benefits offered by this job

Healthcare benefits
401(k) with company match
Employee stock purchase plan

Job summary

Anika Therapeutics is seeking a Sr. Aseptic Manufacturing Technician for 2nd shift (1:00pm-9:30pm) in Bedford, MA. You will perform aseptic fills, operate equipment, and ensure compliance with GMP and QA standards.

The role requires 4–6 years in cGMP manufacturing, strong communication, and ability to work flexible hours in a regulated cleanroom environment. Comprehensive benefits and a total rewards package are offered.

Qualifications

  • High school diploma or GED or equivalent experience.
  • 4–6 years of related experience in a cGMP manufacturing environment.
  • Ability to work flexible hours
  • Strong written and verbal communication skills.
  • Proficiency with Microsoft Office applications.
  • Ability to gown and access cleanroom areas and wear PPE.
  • Ability to lift 25–50 lbs and stand up to 6 hours.

Responsibilities

  • Operate production equipment per SOPs, MDs, and OPMs.
  • Execute aseptic fills including transfer, setup, sanitization, autoclaving, and process simulation.
  • Perform scheduled cleaning and sterilization of equipment.
  • Support changeover activities and troubleshoot process issues.
  • Initiate work orders and review manufacturing docs for compliance.
  • Coordinate sample prep and testing; record data in Batch Records and logs.
  • Maintain Good Documentation Practices and document revisions.
  • Report deviations and nonconformance to management.

Skills

Communication skills
Computer skills
Attention to safety
Flexibility

Education

High school diploma or GED

Tools

SAP

Job description

Anika Therapeutics is seeking a Sr. Aseptic Manufacturing Technician for 2nd shift (1:00pm-9:30pm) in Bedford, MA. You will perform aseptic fills, operate equipment, and ensure compliance with GMP and QA standards.

The role requires 4–6 years in cGMP manufacturing, strong communication, and ability to work flexible hours in a regulated cleanroom environment. Comprehensive benefits and a total rewards package are offered.

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