Manufacturing Technician at Smart Biotech Solutions
Bedford, MA 01730, USA -
Full Time


Start Date

Immediate

Expiry Date

21 Oct, 25

Salary

22.0

Posted On

21 Jul, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Gowns, Ppe, Gloves, Ged, Production Experience, Computerized Systems, Production Equipment, Manufacturing

Industry

Pharmaceuticals

Description

Position: Manufacturing Technician I (2 Openings)
Location: Bedford, MA
Duration: 3–6 Month Contract (Potential to Extend)
Start Date: ASAP
Pay Range: $20–$22/hr
Schedule: Full-time, flexible hours as required by production

POSITION SUMMARY:

We are seeking two Manufacturing Technicians I to join a fast-paced biotech/pharmaceutical team in Bedford, MA. One technician will focus on aseptic manufacturing, and the other on crosslink operations. These are contract roles with potential for long-term engagement, offering excellent entry into the pharmaceutical/medical device manufacturing field.

MINIMUM QUALIFICATIONS:

  • High school diploma or GED
  • 0–1+ years of manufacturing or production experience (pharma/biotech/medical device a plus)
  • Willingness to work flexible hours and shifts
  • Ability to:
  • Stand for extended periods (up to 6 hours)
  • Lift, push, or pull up to 25–50 lbs
  • Climb ladders and work on elevated platforms
  • Wear required PPE (goggles, gloves, gowns, safety shoes)
  • Work around alcohols, acids, and bases

PREFERRED EXPERIENCE:

  • Prior cleanroom or aseptic technique experience
  • Manufacturing background in the medical device or biotech industries
  • Experience with automated production equipment
  • Familiarity with computerized systems and data entry

How To Apply:

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Responsibilities

OPEN ROLES:

  • Aseptic Manufacturing Technician I
  • Crosslink Manufacturing Technician I

KEY TACTICAL RESPONSIBILITIES:

  • Operate production equipment in accordance with SOPs, Batch Records, and Manufacturing Directions (MDs)
  • Execute procedures related to aseptic fills: transfer, set-up, sanitization, autoclaving, and process simulations
  • Perform solvent recovery, clean-in-place (CIP), and clean-out-of-place (COP) tasks for complex equipment
  • Assist in troubleshooting and resolving production issues
  • Record data accurately in batch records and logbooks per Good Documentation Practices (GDP)
  • Report procedural deviations and non-conformance to management
  • Maintain current training records, including classroom and on-the-job instruction

ROLE COMPLEXITY:

Work is routine but requires adherence to cGMP and sterile practices. The ideal candidate will receive clear instructions and support for new tasks while demonstrating flexibility and accountability.

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