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Healthcare & Medical 🏢 Contract ⭐️ Terverifikasi

Senior QC Associate - Projects (2-Year Contract)

GSK
Canggu, Ubud, Denpasar, Jimbaran, Nusa Dua, Kuta, Badung
Salary Estimate
Rp 15.000.000 – Rp 25.000.000
Newest
Live Update
18 Juli 2026
Deadline
18 Jul 2027

job description

Join GSK, a global leader in healthcare, as a Senior QC Associate - Projects in our dynamic team based in Bali. This is a unique opportunity to contribute to life-saving pharmaceuticals while enjoying the vibrant culture and lifestyle of Bali. In this role, you will play a pivotal part in ensuring the quality and compliance of our products through rigorous analytical testing and project management.

As a Senior QC Associate, you will work on cutting-edge projects, collaborate with cross-functional teams, and uphold the highest standards of quality control. This 2-year contract position offers a competitive salary, professional growth, and the chance to make a real impact in the healthcare industry.

If you are a detail-oriented professional with a passion for quality and a background in pharmaceuticals or life sciences, we invite you to apply and become part of our mission to improve global health.

Responsibility

  • Perform analytical testing of pharmaceutical products using advanced laboratory techniques.
  • Manage and track samples throughout the testing process, ensuring accuracy and compliance.
  • Collaborate with cross-functional teams to support project timelines and deliverables.
  • Maintain detailed records of test results and laboratory activities in accordance with GMP standards.
  • Troubleshoot and resolve technical issues related to testing equipment and methodologies.
  • Participate in the validation and qualification of new analytical methods.
  • Ensure adherence to safety, quality, and regulatory guidelines in all laboratory operations.
  • Provide training and mentorship to junior team members as needed.

Qualifications

  • Bachelor's degree in Chemistry, Pharmacy, Biochemistry, or a related field.
  • Minimum of 3 years of experience in a Quality Control or analytical laboratory setting.
  • Strong knowledge of GMP, GLP, and other regulatory requirements.
  • Experience with analytical techniques such as HPLC, GC, UV-Vis, and dissolution testing.
  • Excellent attention to detail and problem-solving skills.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Proficient in laboratory information management systems (LIMS) and Microsoft Office.
  • Strong communication skills in English, both written and verbal.

Required Skills

Quality Control Analytical Testing GMP HPLC GC LIMS Pharmaceuticals Laboratory Management

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