GMP Manufacturing Technician II - Night Shift

Catalent, Inc.

Chelsea (MA)

On-site

USD 34,000 - 40,000

Full time

15 hours ago
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Benefits offered by this job

Medical, dental, and vision benefits
Paid time off + 8 holidays
Tuition Reimbursement

Job summary

Catalent's Chelsea, Massachusetts site is a GMP facility serving as a Center of Excellence for spray dry dispersion and dry powder inhaler manufacturing. We seek a Pharmaceutical Technician II to independently execute GMP unit operations, ensure documentation integrity, and support troubleshooting across multiple areas in a 2/2/3 shift, onsite in Chelsea, MA.

The role emphasizes reliable production, deviation investigations support, and collaboration with Maintenance, QA, and Engineering to

Qualifications

  • High School diploma or GED required.
  • Minimum of 1 year manufacturing experience.
  • Must have strong documentation skills.
  • Ability to lift up to 40lbs. as needed.

Responsibilities

  • Execute GMP manufacturing operations independently across multiple unit operations such as spray drying, blending, encapsulation, and packaging
  • Ensure completeness and accuracy of documentation
  • Coordinate material handling and staging activities
  • Assist in deviation investigations; Perform basic troubleshooting of equipment and process deviations
  • Identify and recommend process improvements; Adjust equipment within defined process limits
  • Interface with Maintenance, Quality Assurance, and Engineering as needed
  • Perform all other duties as assigned

Skills

Documentation skills
GMP knowledge
Equipment handling

Education

High School diploma or GED

Job description

Catalent's Chelsea, Massachusetts site is a GMP facility serving as a Center of Excellence for spray dry dispersion and dry powder inhaler manufacturing. We seek a Pharmaceutical Technician II to independently execute GMP unit operations, ensure documentation integrity, and support troubleshooting across multiple areas in a 2/2/3 shift, onsite in Chelsea, MA.

The role emphasizes reliable production, deviation investigations support, and collaboration with Maintenance, QA, and Engineering to

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