Senior Scientist, Stability Management

WuXi XDC; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

WuXi XDC in Singapore is seeking a QC sample management specialist to ensure proper handling of in-process and release samples for product, environmental and raw materials. You will oversee stability sample management and regulatory retaining of samples, while supporting QC instrument management and calibration of analytical tools such as HPLC, GC, IC and LC-MS.

You will assist in electronic system applications including LIMS, Empower and LES, and guarantee all QC activities comply with cGMP,

Qualifications

• Bachelor’s degree or higher in pharmacy, chemistry, biochemistry, analytical chemistry, or related disciplines.
• Minimum 5 years of pharma industry experience with cGMP compliance.

Responsibilities

• Manage in-process and release samples for product, environmental, and raw materials.
• Ensure stability and regulatory retaining of samples.
• Assist QC instrument management for HPLC, GC, IC, LC-MS and general lab equipment.
• Support electronic systems (LIMS, Empower, LES) and ensure data integrity and EHS compliance.

Skills

Sample management

Quality mindset

Regulatory awareness

GxP compliance

Education

Bachelor’s degree or higher in pharmacy, chemistry, biochemistry, analytical chemistry, or related disciplines

Tools

LIMS

EMPOWER

LES

Job description

• Perform sample management, including but not limited to:
• Managing in-process and release samples for product, environmental, and raw material management.
• Stability sample management.
• Regulatory retaining of sample management.
• Assist in QC instrument and equipment management, such as C-type instruments including HPLC, GC, IC, and LC-MS, as well as B-type instruments like pH meters, balances, and color meters.
• Assist in electronic system applications, including but not limited to LIMS, EMPOWER, and LES.
• Ensuring all activities within the QC team are performed in compliance with cGMP, data integrity, and EHS requirements.

Qualifications

• Bachelor’s degree or higher in pharmacy, chemistry, biochemistry, analytical chemistry, or other related disciplines with minumum 5 years of working experience in pharma industry.
• Thorough knowledge of cGMP compliance principles and management, with a strong quality mindset.