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Manufacturing, Transportasi & Logistik 🏢 Contract ⭐️ Terverifikasi

Analytical Development Analyst

Combiphar
Padalarang, Jawa Barat
Estimasi Gaji
Rp 4.000.000 – Rp 7.000.000
Live Update
1 Juli 2026
Batas Akhir
1 Jul 2027

Deskripsi Pekerjaan

Are you ready to leverage your analytical skills to drive quality and innovation in the pharmaceutical sector? Combiphar is actively seeking a talented Analytical Development Analyst to join our dedicated team in Padalarang, Jawa Barat. In this pivotal contract position, you will be at the forefront of our quality assurance and product development initiatives, ensuring that every product meets rigorous industry standards.

As an Analytical Development Analyst, you will dive deep into complex data sets, designing and validating analytical methods that streamline our production processes. You will act as a bridge between our technical teams and management, providing critical insights that support decision-making and regulatory compliance. Combiphar prides itself on a culture of continuous improvement and scientific excellence, offering you the opportunity to grow your expertise in a supportive environment.

Join us to make a tangible impact on the industry while enjoying a competitive package and a collaborative workplace culture.

Tanggung Jawab

  • Conduct comprehensive data analysis on manufacturing processes to identify trends, variances, and areas for process improvement.
  • Develop, validate, and optimize analytical methods for raw materials, intermediates, and finished products.
  • Prepare detailed technical reports and presentations for management and regulatory bodies.
  • Ensure strict adherence to Good Manufacturing Practices (GMP) and quality control standards.
  • Collaborate with cross-functional teams, including R&D and Quality Assurance, to support product launches.
  • Monitor and troubleshoot analytical instruments to ensure data accuracy and reliability.
  • Maintain accurate documentation of all analytical procedures and results in compliance with company policies.

Kualifikasi

  • Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, or a related scientific field.
  • 1-3 years of experience in analytical development, quality control, or a similar role within the manufacturing or pharmaceutical industry.
  • Strong proficiency in data analysis tools such as Microsoft Excel (pivot tables, VLOOKUP) and statistical software (e.g., R, Python, JMP).
  • Understanding of GMP regulations and quality management systems.
  • Excellent problem-solving skills and attention to detail.
  • Effective communication skills, both written and verbal, in a technical environment.
  • Ability to work independently and meet tight deadlines in a fast-paced setting.

Keahlian yang Dibutuhkan

Data Analysis Quality Control Manufacturing GMP SQL Excel Statistical Analysis Process Improvement Problem Solving Chemical Engineering

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