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Job Requirment

  • Position:

    Production Pharmacist

    Occupation:

    Medical Services

    Sub Occupation:

    Pharmaceutical

  • Position:

    Production Pharmacist

    Occupation:

    Manufacturing/QA-QC

    Sub Occupation:

    Production Planning/Control

Job Location

Bangkok (All)

Samut Prakarn (All)

Latest Salary

40,000 - 55,000 THB

Job Type

Full time

Availability

within 30 days

Working Bangkok

Yes

Work Upcountry

Yes

Willing to work oversea?

Yes

Education

2024 - Srinakharinwirot University

Faculty:Pharmacy
Major:Industrial Pharmacy
GPA 3.58 - Bachelor's Degree

Experience/ Internship

January 2024 toMarch 2026  (2 Year 2 Month)
  • Last Position:
  • Production Pharmacist

Job Description

  • Manufacturing Operations
  • - Monitored semi-solid and liquid dosage form manufacturing processes and provided technical support for tablet manufacturing operations involving targeted therapy products in a closed system, ensuring GMP compliance.
  • - Investigated and resolved on-site production issues, ensuring adherence to GMP standards and reducing operational disruptions.
  • - Ensured production area readiness in compliance with GMP standards, including verification of equipment, material availability, and controlled environmental conditions to support continuous manufacturing operations.
  • - Created, reviewed, and verified Batch Manufacturing/Packaging Records (BMR/BPR) to ensure accuracy, completeness, and GMP compliance.
  • - Coordinated with equipment manufacturers and external service providers to investigate and resolve equipment-related issues, minimizing operational downtime and safeguarding product quality.
  • Cross-functional Coordination
  • - Collaborated cross-functionally with R&D, QA, QC, Warehouse, and Engineering to ensure material availability, equipment readiness, and resource alignment before production initiation.
  • - Supported Process Validation (PV) and Process Qualification (PQ) activities in collaboration with Quality Assurance (QA).
  • - Supported troubleshooting activities during Technology Transfer of targeted therapy (solid dosage forms) in collaboration with R&D throughout trial batch and production preparation.
  • GMP Compliance and Documentation
  • - Prepared, reviewed, and maintained production documentation, including SOPs, BMRs, and BPRs, in accordance with GMP requirements.
  • - Participated in deviation handling and investigation, coordinating with QA to support CAPA implementation.
  • - Supported Change Control activities related to manufacturing processes, equipment, and materials, including impact assessment and implementation in collaboration with QA.
  • - Prepared production-related documentation to support product registration.
  • Training, Procurement, and Budget Support
  • - Conducted GMP, SOP, and basic machine operation training for production operators to reinforce compliance awareness and ensure disciplined execution of manufacturing procedures.
  • - Supported procurement activities for raw materials, packaging materials, and production-supporting materials.
  • - Prepared annual budget proposals and monitored expenditures to ensure alignment with approved financial plans.

Hard Skill

  •  - Technology transfer / Beginner
  •  - Documentation complied with GMP requirements / Beginner
  •  - Change control and deviation / Beginner
  •  - GMP and regulatory compliance / Beginner
  •  - Manufacturing process understanding / Beginner
  •  - Cross-functional coordination / Beginner
  •  - Semi-solid and solid dosage forms operation / Beginner
  •  - Corrective action and Preventive action (CAPA) / Beginner

Soft Skill

  •  - Able to work under pressure
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