Associate Research Scientist

Macsen Laboratories; Debari; On-site; INR 550,000 - 900,000; Full time

Job summary

Macsen Laboratories in India is seeking a chemist with experience on HPLC, GC and LC-MS to join our analytical team. The role involves preparation of volumetric solutions, mobile phases and reagents, and operation of advanced instruments.

You will perform method development and validation, support stability studies, review SOPs and reports, and ensure GMP-compliant lab records. The position requires shift work and strong teamwork with R&D and QA.

Qualifications

• Experience on handling sophisticated instruments like HPLC/GC/LC-MS.
• Willingness to work in shift system.
• Familiar with SOPs, GMP, and safety norms.

Responsibilities

• Handle instruments such as HPLC, GC and LC-MS and ensure accurate analyses.
• Prepare volumetric solutions, mobile phases, and reagents.
• Assist with method development and validation and instrumental analysis.
• Support stability studies for new and existing products as required.
• Prepare and review SOPs, protocols, reports and relevant ARD documentation.
• Manage reagents and consumables and ensure regulatory compliance.
• Maintain lab records and logbooks per GMP and safety guidelines.
• Work independently and collaborate with R&D and QA teams.
• Handle samples from R&D (Synthesis) including in-process monitoring and finished products.

Skills

HPLC

GC

LC-MS

Job description

Job Responsibility:

Candidate should have Experience on handling sophisticated instruments Such as HPLC, GC, and LC-MS.

Available to working in shifting system.

1. Expertization on Preparation of Volumetric solution, Mobile phase, and Reagent.

2. Familiar with hand-holding for operation and handling of the latest laboratory instruments, Apparatus, and software (HPLC/GC/LCMS/GCMS, etc.)

3. Working Knowledge of Good chromatographic practices and Troubleshooting related to sophisticated instruments like HPLC/GC, etc.

4. Sound knowledge of Method development & Method validation, instrumental method of analysis, and logical approach.

5. Manage Stability & shelf-life Studies for new product /existing product as and when required.

6. Analysis of samples received from R&D (Synthesis) (Samples include in-process Reaction monitoring, intermediate, finished product.

7. Responsible for the preparation and review of SOPS, protocol, Reports and relevant documentation of ARD.

8. Manage all reagent and consumable Requirements.

9. Knowledge of Different regulatory guidelines.

10. Capable of working independently and handling laboratory operations if required.

11. Maintain lab records and logbooks according to GMP.

12. Familiar with handling chemicals, pharmaceutical product samples, and aware of laboratory safety norms and PPE usage.

Required Candidate Profile:

Experience in handling instruments like HPLC, GC, and LC-MS.

Behavioral skill:

• Strong Commitment towards work and a high level of dedication, enthusiasm, and motivation


• Persuasive ability in a team and cross-functional environment.


• Good speaking, listening, and writing skills, attention to detail, and a proactive self-starter.


• Ability to work successfully in a dynamic environment and meet tight deadlines.


• Ability to develop new ideas and creative solutions.


• Support Team members by providing peer feedback.


• Foster an environment of knowledge sharing within the Team.


• Maintain healthy working relationships with the related teams and departments in Research & Development.