GMP Manufacturing/Bioprocess Technician

Job Title :GMP Manufacturing/Bioprocess Technician

Location: Onsite Frederick MD

Contract: 12 months (with possibility of conversion)

Hours: 6am-6:30pm

Shift: Days (2-2-3 schedule)

PR: $26/hr

Manufacturing Technician I / Bioprocess Technician (Day Shift) – Frederick, MD

Job Summary

The Manufacturing Technician I is responsible for operating upstream, downstream, and central services processing equipment in a biopharmaceutical manufacturing environment. This role supports production activities by following established Standard Operating Procedures (SOPs), Master Production Records (MPRs), and cGMP requirements to ensure safe, compliant, and efficient manufacturing operations.

Key Responsibilities

• Operate bioprocess manufacturing equipment according to SOPs, MPRs, SPRs, and cGMP requirements.
• Perform manufacturing activities including:
• Solution preparation
• Cell culture operations
• Purification processes
• Formulation activities
• Supporting production operations
• Train under qualified technicians to gain proficiency and equipment qualification.
• Complete and maintain accurate cGMP documentation.
• Utilize Manufacturing Execution Systems (MES) for production activities and recordkeeping.
• Assist with troubleshooting and problem-solving for non-routine manufacturing issues.
• Participate in continuous improvement initiatives within manufacturing operations.
• Follow company safety policies, values, and operational standards.
• Perform additional duties as assigned.

Required Qualifications

• High School Diploma or equivalent.
• 0–1 year of manufacturing, laboratory, production, or related experience.
• Basic computer proficiency.
• Ability to follow written procedures and instructions.
• Ability to work independently and within a team environment.
• Understanding of or willingness to learn cGMP regulations and compliance requirements.

Preferred Qualifications

• Bachelor's degree (BS/BA) preferred.
• Degree in a STEM field (Biology, Chemistry, Biotechnology, Engineering, etc.).
• Prior exposure to:
• Aseptic manufacturing
• GMP/cGMP environments
• Pharmaceutical, biotechnology, or life sciences manufacturing

Work Environment

• Biopharmaceutical manufacturing facility.
• Requires adherence to GMP and safety standards.
• Fast-paced production environment with strict quality and compliance requirements.

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