Key Responsibilities:

• 
  Perform inspection and testing of raw materials, in-process, and finished goods.
• 
  Document results, complete batch records, and generate QC reports.
• 
  Maintain Device History Records (DHR) and ensure compliance with cGMP and regulatory requirements.
• 
  Conduct data analysis and support process monitoring and trending.
• 
  Investigate Out of Specification (OOS) results and support CAPA activities.
• 
  Perform routine maintenance and calibration checks of lab equipment.
• 
  Support environmental monitoring and maintain QC lab readiness.
• 
  Assist in reagent formulation and manufacturing activities.
• 
  Manage lab inventory, supplies, and vendor coordination.
• 
  Participate in validations, method development, and process transfers.

Quality & Compliance:

• 
  Ensure adherence to FDA, ISO, GMP, and OSHA standards.
• 
  Maintain accurate documentation for material handling, storage, and release.
• 
  Support audits, safety reporting, and quality system compliance.

Qualifications:

• 
  High School Diploma (Associate’s or Bachelor’s in Life Sciences preferred).
• 
  0–7 years of experience in a laboratory or regulated industry.
• 
  Experience in cGMP/GLP/ISO environments preferred.

Skills & Requirements:

• 
  Strong analytical, troubleshooting, and data analysis skills.
• 
  Hands-on lab experience (pipetting, titration, spectroscopy, etc.).
• 
  Excellent documentation and organizational skills.
• 
  Ability to work in a fast-paced, team-oriented environment.
• 
  Familiarity with Lean/6S practices is a plus.

Company Benefits:
Medical, Dental, Vision, Paid Sick
leave, 401K
If interested, please share your update resume at
hr@dawarconsulting.com
/
kavitha@dawarconsulting.com