Rubicon is hiring an Officer for its Analytical Department at Thane. This role is suitable for candidates with M. Pharm or M. Sc qualification and 1-2 years of experience in analytical development or related pharmaceutical laboratory work. The selected candidate will work as an analyst in an analytical development lab supporting pharmaceutical formulation development for solid oral and liquid oral dosage forms.
The position involves routine and stability analysis, support for method development, instrument handling, GMP/GLP documentation, troubleshooting, and analytical support for formulation development projects. Candidates should be comfortable working across shifts and visiting external sites when required by project needs.
Job Details
| Position | Officer |
| Department | Analytical Department |
| Reporting To | Assistant General Manager |
| Location | Thane |
| Experience | 1-2 years |
| Dosage Form | Solid Oral / Liquid Oral |
Role Overview
The Officer will support analytical development activities for pharmaceutical formulation development, mainly for solid oral and liquid oral products. The role includes performing dissolution, assay and RS testing, supporting method development activities, maintaining accurate laboratory records and contributing technical inputs during investigations and troubleshooting.
Key Responsibilities
- Perform routine and stability analysis of dissolution, assay and RS tests for assigned products.
- Support method development of dissolution, assay and RS for solid oral and liquid oral products in line with regulatory requirements.
- Provide analytical inputs and observations during analysis to help identify root causes of failures or OOT data.
- Maintain online logbooks, data entries and LNB entries as required.
- Follow GMP and GLP practices during laboratory activities.
- Read technical papers, research articles and new guidelines, and participate in internal scientific discussions.
- Perform calibration of instruments as per schedule.
- Provide technical inputs for troubleshooting and resolving analytical issues.
- Conduct development and stability studies as per the approved plan.
Required Qualifications
- M. Pharm / M. Sc
Experience Required
- 1-2 years of experience
- Exposure to solid oral and liquid oral dosage forms
Required Knowledge and Skills
- Knowledge of handling HPLC
- Knowledge of handling KF titrator
- Knowledge of handling dissolution tester
- Understanding of GMP / GLP practices
- Ability to support dissolution, assay and RS method development activities
- Ability to contribute observations and inputs during OOT or failure investigations
Additional Requirements
- Candidate is expected to work in all shifts.
- Candidate is expected to visit external sites as per projects requirements.
Why This Role Is a Good Opportunity
This role offers hands-on exposure to analytical development activities for solid and liquid oral pharmaceutical products. It is a strong opportunity for M. Pharm or M. Sc candidates with early-career experience who want to build practical expertise in dissolution, assay, RS testing, method development support, stability studies, instrument handling and regulated laboratory documentation.
How to Apply
Interested candidates can apply through the official job application page.
