Analytical Chemistry Research Associate – Method Validation

Lupin Ltd; Indiana; On-site; USD 60,000 - 85,000; Full time

Job summary

Lupin Ltd in Indiana is seeking an analytical chemist with hands-on experience operating advanced instruments like HPLC, GC, dissolution, and Karl Fischer. The role requires working in the analytical section with strict GDP practices and experience in drug product method validation.

The ideal candidate will prepare and execute protocols and reports for validation and equivalency studies while maintaining rigorous laboratory safety standards and regulatory compliance.

Qualifications

• Hands-on experience operating advanced analytical instruments such as HPLC, GC, Dissolution and Karl Fischer (KF).
• Worked effectively in the analytical section, adhering strictly to Good Documentation Practices (GDP).
• Experienced in method validation for drug products in compliance with quality standard.
• Skilled in preparation and execution of protocols and reports for method validation and method equivalency studies.
• Thorough knowledge of laboratory safety procedures and compliance with established safety guidelines.

Responsibilities

• Operate advanced analytical instruments (HPLC, GC, Dissolution, Karl Fischer) and related equipment.
• Adhere to GDP and maintain high-quality documentation practices.
• Conduct method validation activities for drug products per quality standards.
• Prepare and execute validation protocols and reports for equivalency studies.
• Maintain strict laboratory safety compliance and procedures.

Skills

HPLC

GC

Dissolution

Karl Fischer (KF)

GDP

Method validation

Protocols & reports

Laboratory safety

Education

Masters in Analytical Chemistry

Job description

Lupin Ltd in Indiana is seeking an analytical chemist with hands-on experience operating advanced instruments like HPLC, GC, dissolution, and Karl Fischer. The role requires working in the analytical section with strict GDP practices and experience in drug product method validation.

The ideal candidate will prepare and execute protocols and reports for validation and equivalency studies while maintaining rigorous laboratory safety standards and regulatory compliance.