Fusion Scientific Laboratories Walk-in On 12th to 19th Jun for Multiple Positions

WALK IN !!!!!

Time and Venue

• 12th June – 19th June , 10.30 AM – 3.00 PM
• Fusion Scientific Laboratories Pvt Ltd
• Plot no. R- 656, MIDC, TTC Industrial Area, Near Golden Garage Rabale, Navimumbai- 400708

Openings Details 

• Position: Research Analyst / Senior Research Analyst / Executive / Senior Executive Analytical Development Laboratory (ADL)
• Experience: 1 to 5 Years
• Department: Analytical Development Laboratory (ADL)

About the Role

We are seeking dynamic, detail-oriented, and motivated professionals to join our Analytical Development Laboratory (ADL) team. The ideal candidate will have hands-on experience with advanced analytical instruments such as HPLC, LCMS, GC, and GCMS and a strong understanding of analytical method development and validation for pharmaceutical products.

The role involves developing and validating analytical methods, performing routine and stability sample analysis, and supporting analytical activities for drug substances and drug products in compliance with regulatory requirements.

Key Responsibilities:

• Develop analytical methods for drug substances and drug products using HPLC, LCMS, GC, and GCMS.
• Perform analytical method validation in accordance with ICH, USFDA, EMA, and other applicable regulatory guidelines.
• Conduct routine testing and stability sample analysis using validated analytical methods.
• Operate, calibrate, maintain, and troubleshoot analytical instruments to ensure uninterrupted laboratory operations.
• Prepare and review analytical protocols, method development reports, validation reports, specifications, and SOPs.
• Investigate analytical deviations, OOS/OOT results, and support root cause analysis and CAPA implementation.
• Ensure data integrity, accurate documentation, and compliance with GMP and GLP requirements.
• Collaborate with Formulation Development, Quality Assurance, Regulatory Affairs, and other cross-functional teams to achieve project milestones.
• Participate in internal and external audits and ensure compliance with cGMP, GLP, and regulatory expectations.

Required Qualifications & Skills

• Master’s Degree in Pharmaceutical Sciences, Analytical Chemistry, or a related discipline.
• 1 to 5 years of relevant experience in pharmaceutical analytical development.
• Hands-on expertise in operating and troubleshooting HPLC, LCMS, GC, and GCMS systems.
• Strong knowledge of analytical method development, optimization, and validation.
• Sound understanding of ICH, USFDA, EMA, and other applicable regulatory guidelines.
• Good documentation practices and experience with GMP/GLP environments.
• Strong analytical, problem-solving, and communication skills.
• Ability to work effectively in a collaborative and fast-paced research environment.