QC Pharmacist Staff

PT. Medifarma Laboratories; Depok; On-site; IDR 100,000,000 - 200,000,000; Full time

Job summary

An established industry player is seeking a dedicated Apothecary to join their dynamic team. In this role, you will be responsible for conducting essential testing and ensuring compliance with Good Manufacturing Practices. Your expertise will support the Quality Control Department in optimizing output and maintaining high standards. This position offers a unique opportunity to contribute to best practices within a reputable organization, where your skills and commitment to excellence will be valued. If you are a responsible and fast learner with strong leadership capabilities, this is the perfect chance to advance your career in a collaborative environment.

Qualifications

• Minimum 1-2 years experience as an Apothecary.
• Training in Good Manufacturing Practices (CPOB) is essential.

Responsibilities

• Conduct testing to sample P&G according to approved procedures.
• Assist QC Manager in managing activities and resources in QC Department.

Skills

Good Manufacturing Practices (CPOB)

Fluent in English

Leadership Skills

Teamwork

Fast Learner

Responsibility

Education

Apothecary Certification

Tools

Specification-met tools

Job description

Requirement

• Apothecary with minimum 1-2 years experience
• Responsible, hard worker, fast learner, and strong leadership
• Able to work individually and with team as well
• Have received training and understand the Good Manufacturing Practices (CPOB)
• Fluent in English both speaking and writing

Job Description

• Responsible for conducting all testing to sample P&G according to procedures / SOP that has been approved along with using specification-met tools and materials
• Assist QC Manager in managing all activities and human resources available in order to optimize output of QC Department
• Review disposition of Stability and manage storage and scheduling stability sampling
• Prepare protocol and P&G stability testing report
• Monitor the temperature of the chamber and review data from thermohygro, as well as evaluate if there is a deviation
• Actively participate in supporting “best practice” execution available in PT. Medifarma Laboratories