Work Hours: 24-36 hours per week
About the Role: In this position, you will play a vital role within a team of QC analysts, where your knowledge and experience will be instrumental in carrying out your responsibilities effectively. In addition to core tasks, you will also be responsible for one or more focus areas. Your primary responsibilities include:
Key Responsibilities:
- Developing and validating analytical methods for release and stability studies using UPLC-PDA, or providing support in this regard.
- Processing, assessing, interpreting, and evaluating analytical results.
- Contributing to the continuous improvement of quality.
- Drafting, authorizing, and reviewing validation protocols/reports.
- Establishing an efficient communication structure with other internal departments.
- Handling various other QC-related tasks.
Qualifications, Experience, and Skills:
- Hold an MLO or HLO diploma.
- Ability to work both independently and as part of a team.
- Previous 2 years of experience in a GMP environment is advantageous.
- Proficiency in standard software systems (MS Windows and MS Office).
- Experience with Quality Management Systems (e.g., MasterControl) and operating UPLC's (e.g., Empower) is a plus.
- Strong laboratory knowledge and skills.