Chemist - Laboratory Analysis & Quality Control
Join PT Pacific Bio Industry as a Chemist and play a pivotal role in ensuring product quality and compliance through rigorous laboratory analysis. Based in the vibrant hub of Canggu, Bali, this position offers a unique opportunity to work in a dynamic and innovative environment. You will be responsible for conducting various chemical analyses, ensuring that our products meet stringent quality standards and regulatory requirements. This role is perfect for a professional who is passionate about chemistry and committed to maintaining high-quality standards in the biotechnology industry.
At PT Pacific Bio Industry, we are dedicated to advancing biotechnology and developing cutting-edge solutions. Our mission is to deliver high-quality products that meet the needs of our customers and comply with international standards. As a Chemist, you will be part of a team that works closely with researchers, production teams, and quality assurance professionals to ensure that our products are safe, effective, and reliable.
๐ Tanggung Jawab Pekerjaan
- Conduct various chemical analyses using state-of-the-art laboratory equipment such as HPLC, GC, and spectrophotometry.
- Ensure that all products meet quality standards and regulatory requirements through rigorous testing and validation.
- Develop and implement standard operating procedures (SOPs) for laboratory analysis.
- Collaborate with the research and development team to support new product development and optimization.
- Participate in quality assurance activities, including audits and inspections.
- Maintain accurate and detailed laboratory records and reports.
- Stay updated with the latest advancements in chemical analysis and quality control methodologies.
- Provide technical support and training to laboratory staff as needed.
๐ Kualifikasi & Syarat
- Bachelor's degree in Chemistry, Chemical Engineering, or related field.
- Minimum of 3 years of experience in laboratory analysis and quality control in the biotechnology or pharmaceutical industry.
- Proficiency in using laboratory equipment such as HPLC, GC, and spectrophotometry.
- Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Certification in ISO 17025 or equivalent quality management systems is a plus.
- Strong analytical and problem-solving skills.
- Excellent communication and teamwork abilities.
- Ability to work in a fast-paced and dynamic environment.
๐ ๏ธ Keahlian
Kirim lamaran sekarang sebelum batas waktu.๐ Lamar Sekarang