Biotech Manufacturing Process Associate I

Meso Scale Diagnostics, LLC.

Rockville (MD)

On-site

USD 46,000 - 66,000

Full time

34 hours ago
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Benefits offered by this job

401(k) plan with company matching
Paid vacation
Paid holidays
Disability insurance

Job summary

Meso Scale Diagnostics, LLC. is seeking a manufacturing technician in Rockville, MD to produce assay kit components and support development timelines.

The role involves operating multiple production lines, troubleshooting automated equipment, and maintaining strict documentation standards. The position requires a biology/chemistry-related degree and at least one year of relevant experience; familiarity with GMP/ISO processes is a plus.

Qualifications

  • Bachelor degree in Biology, Chemistry, Biotechnology, Engineering or related field or associate’s degree with equivalent experience.
  • One year of relevant experience desired.
  • Experience working independently in manufacturing or research lab highly preferred.
  • Familiarity with cGMP and ISO 9001 is a plus.
  • Knowledge of automated equipment function and use.

Responsibilities

  • Manufacture custom and/or prototype requests for internal and external customers.
  • Operate multiple production lines (Plate, Reagent and/or BioChemical manufacturing).
  • Assist with operating and troubleshooting automated equipment used to perform and produce biological assays/reagents.
  • Document data entries, logs, batch records and inventory.
  • Draft standard operating procedures and batch records for new products.

Skills

Analytical skills
Mechanical aptitude
Communication skills
Multi-tasking

Education

Bachelor degree in Biology, Chemistry, Biotechnology, Engineering or related field
Associate’s degree with equivalent experience
Bachelor of Science in Biology or related field
Bachelor of Science in Chemistry or related field

Tools

MRP/ERP systems
JDE

Job description

Meso Scale Diagnostics, LLC. is seeking a manufacturing technician in Rockville, MD to produce assay kit components and support development timelines.

The role involves operating multiple production lines, troubleshooting automated equipment, and maintaining strict documentation standards. The position requires a biology/chemistry-related degree and at least one year of relevant experience; familiarity with GMP/ISO processes is a plus.

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