Manufacturing Associate I - Night Shift (GMP, Onsite)

Catalent

Harmans (MD)

On-site

USD 36,000 - 43,000

Full time

5 days ago
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Benefits offered by this job

Medical, dental, and vision benefits
Career development
Paid time off
8 paid holidays

Job summary

Catalent's Harmans, MD facility is seeking an Associate I, Manufacturing to support upstream or downstream production. You will perform cGMP activities, operate process equipment, and help create and revise manufacturing documents on the floor, including weekend shifts on a 2-2-3 schedule.

This onsite role requires a high school diploma with GMP experience or a science/engineering degree plus GMP exposure, ability to lift up to 40 pounds, and strong teamwork and English communication on a

Qualifications

  • GMP manufacturing experience and understanding of validated processes.
  • Ability to interpret batch records and SOPs in a GMP setting.
  • Team coordination and clear written/verbal communication.
  • Flexibility to work nights, weekends, and overtime.

Responsibilities

  • Execute cGMP manufacturing processes and support activities per batch records and SOPs.
  • Document, maintain, and verify equipment records and production data.
  • Weigh, dispense, label, stage, and transfer raw materials for production.
  • Prepare media/buffer solutions and operate process equipment.
  • Set up, operate, clean, sanitize, and troubleshoot production equipment.
  • Disassemble/assemble equipment and support validation/change control tasks.
  • Maintain logs, inventory, and cleaning records for production rooms.
  • Participate in training and continuous proficiency development.
  • Perform other duties as assigned.

Skills

GMP manufacturing experience
Teamwork
Communication skills
Fluent English
Shift flexibility
Physical stamina

Education

High School Diploma or equivalent
Associate's Degree in science/engineering/biotech
Bachelor's Degree in science/engineering

Job description

Catalent's Harmans, MD facility is seeking an Associate I, Manufacturing to support upstream or downstream production. You will perform cGMP activities, operate process equipment, and help create and revise manufacturing documents on the floor, including weekend shifts on a 2-2-3 schedule.

This onsite role requires a high school diploma with GMP experience or a science/engineering degree plus GMP exposure, ability to lift up to 40 pounds, and strong teamwork and English communication on a

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