Research Associate- LBC BIO Analytical

Lupin Ltd; Indiana; On-site; USD 42,000 - 64,000; Full time

Job summary

Lupin Ltd in Indiana is seeking a Research Associate to support method development and validation for analytical molecules, perform sample processing and bio-analysis per SOPs and regulatory guidelines.

You will coordinate with the team for development, validation and study analysis, calibrate equipment, compile raw data, and assist with document archival, requiring 1–2 years of experience and a Master’s degree in Analytical Chemistry or Chemistry.

Qualifications

• Masters in Analytical Chemistry or Chemistry is required.
• 1–2 years of related experience.
• Experience with SOPs and regulatory guidelines.

Responsibilities

• Perform method development and validation for molecules following SOPs and regulatory guidelines.
• Perform sample processing and quantification during method development, method validation and study sample analysis as per SOPs and protocol.
• Conduct bio-analysis of study samples following the validated bioanalytical procedure and applicable regulatory guidelines.
• Plan and coordinate with team for Method Development, Validation and Study sample analysis.
• Implementation of Quality systems and SOPs.
• Calibration of equipment used in Bioanalytical department.
• Compilation of raw data during Method development, validation and study sample analysis.
• Scanning of documents for archival.
• Any Other Responsibilities Assigned By Head-Bioanalytical.

Skills

Method development

Method validation

Bio-analysis

Analytical chemistry

Data analysis

SOP adherence

Education

Master's degree in Analytical Chemistry

Job description

Research Associate

Responsibilities

• To perform Method development and Method validation for various molecules following the SOPs and regulatory guidelines.
• To perform sample processing and quantification during Method development, method validation and study sample analysis as per SOP's and protocol.
• To conduct bio-analysis of the study samples following the validated bioanalytical procedure and applicable regulatory guidelines.
• Planning and coordinating with team for Method Development, Validation and Study sample analysis.
• Implementation of Quality systems and SOP’s.
• Calibration of equipment used in Bioanalytical department.
• Compilation of raw data during Method development, validation and study sample analysis.
• Scanning of documents for archival.
• Any Other Responsibilities Assigned By Head-Bioanalytical.

Work Experience

1 to 2 years

Education

Masters in Analytical Chemistry or Chemistry