Microbiology QC Technician: GMP & Automation Focus

PMFarma

España

Hybrid

PHP 300,000 - 520,000

Full time

14 days+
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Job summary

PMFarma is seeking a highly skilled QC Technician - Microbiology to join our healthcare team. You will oversee lab operations, ensure GMP compliance, and support continuous improvement and automation initiatives.

You will supervise analysts, review analytical documentation, and collaborate on SOPs, methods, and stability protocols. Experience in pharmaceutical QC and strong communication are essential for success.

Qualifications

  • Bachelor's degree in Biology or related field required.
  • Specialization in Microbiology is highly preferred.
  • At least 1 year of QC experience in the pharmaceutical industry.

Responsibilities

  • Ensure compliance with Safety, Environment, and Quality procedures.
  • Supervise analysts in performing laboratory tests and activities.
  • Review and approve test results, certificates of analysis, stability studies, and supplier qualifications.
  • Draft SOPs, specifications, analytical methods, and stability protocols.
  • Manage SAP entries for results, batch management, and material creation.
  • Oversee calibration and qualification of laboratory instruments and maintain related documentation.
  • Lead technical services activities: equipment calibration, qualification, and lifecycle management.
  • Maintain procedures for computerized systems validation and ensure data integrity.
  • Support audits and inspections by health authorities; assist in regulatory inquiries.

Skills

Quality Control
Microbiology
GMP compliance
Documentation & record-keeping
Communication skills

Education

Bachelor's degree in Biology or related field

Tools

SAP
Laboratory instruments

Job description

PMFarma is seeking a highly skilled QC Technician - Microbiology to join our healthcare team. You will oversee lab operations, ensure GMP compliance, and support continuous improvement and automation initiatives.

You will supervise analysts, review analytical documentation, and collaborate on SOPs, methods, and stability protocols. Experience in pharmaceutical QC and strong communication are essential for success.

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