We are seeking a LIMS Associate Engineer with 4 to 7 years of experience, specializing in SampleManager LIMS. The ideal candidate will possess strong technical skills, a good understanding of laboratory practices in the pharmaceutical domain, and hands-on experience in LIMS development and configuration.

Key Responsibilities:

Design, develop, and configure SampleManager LIMS modules including:

Sample workflows

Stock module

Instrument module

Instrument Interfacing using Integration Manager

Report Designer, Forms Designer, Label Designer

Sample Scheduler

Batch Management, Lot Management, Plate Handling

Stability, SQC, SM-IDI, PIMS, and Dashboards

Participate in and contribute to at least 1–2 LIMS implementation or development projects.

Handle instrument interfacing, calibration, and maintenance tasks within LIMS.

Write and optimize database queries; support report generation and form design.

Ensure robust testing, documentation, and adherence to validation practices.

Follow ITIL guidelines and support processes for incident and change management.

Collaborate with cross-functional teams and be proactive in taking on technical challenges.

Required Skills & Qualifications:

Strong hands-on experience with SampleManager LIMS development and configuration.

Prior experience in pharmaceutical laboratory practices and GxP environment.

Good understanding of instrument interfacing, calibration, and maintenance integration.

Experience in SQL/DB management, report development, and LIMS form design.

Familiarity with ITIL processes, change control, and support ticket resolution.

Strong analytical, documentation, and validation skills.

Ability to work independently and manage multiple tasks effectively.

Preferred Skills:

Experience with dashboards and KPI reporting within LIMS.

Exposure to SampleManager IDI (SM-IDI), PIMS, and SQC modules.

Knowledge of regulatory compliance (e.g., 21 CFR Part 11, ALCOA+ principles).