Analyst Job Opportunity for B Pharmacy Graduates at Rubicon Research Ltd | Apply Now
If you are searching for a Pharma Job, this Analyst Job opportunity could be a great step in your pharmaceutical career. Rubicon Research Ltd is hiring an Officer (Analyst) in the Quality Control department at its Satara location. This Pharma Job provides professionals the chance to work in a regulated QC laboratory environment performing analytical testing using instruments like HPLC, GC, UV, IR, and dissolution systems. Candidates with 2–5 years of experience in pharmaceutical quality control will find this Analyst Job highly suitable for career growth.
- Job Position: Officer
- Location: Satara
- reqId: 181575
About the Company
Rubicon Research Ltd is a well-known pharmaceutical research and development organization specializing in innovative drug delivery technologies and pharmaceutical product development. The company works with global pharmaceutical partners and operates under strict regulatory compliance including GLP, GDP, and GMP environments. This Pharma Job offers an excellent Analyst Job opportunity for professionals looking to work in advanced analytical laboratories.
Job Description
Rubicon Research Ltd is hiring an Officer (Analyst) in the Quality Control department for its Satara facility. This Pharma Job involves performing analytical testing of raw materials, packaging materials, water samples, in-process samples, finished products, and stability samples.
The selected candidate for this Analyst Job will perform analytical testing using laboratory instruments and ensure compliance with GLP, GMP, and safety standards in the laboratory environment.
Key Responsibilities
- To perform physical and chemical, instrumental analysis of Raw Material, packaging material, Water samples, In Process, Finished Product Samples, and Stability Samples.
- The candidate should have experience in HPLC, GC-UV, IR, and Dissolution testing.
- To perform a Release testing, Dissolution profile study, challenge study, hold time study, RLD sample analysis, validation, verification, method transfer activity, and API-Verification as applicable.
- To perform instrument calibration and working standard qualification.
- Responsible for adherence of GLP and the Health, Safety, and Environment system in the laboratory.
- To perform the task assigned by the supervisor/HOD as and when required.
- Should have good written and communication skills.
Qualifications
Preferably have the following skills, but not limit as mentioned below;
- Bachelor’s / Master’s Degree in Science / Pharma.
- The candidate should have experience in HPLC / GC / UV / IR / KF / Dissolution, etc.
- He should have exposure to QC working under GLP, GDP, and GMP environments.
- The candidate having experience in a US-FDA-approved company is more preferable.
- Knowledge of Chromeleon 7.2 software will be an added advantage.
- Should have the skill to achieve deliverable tasks with minimal support for analysis.
Additional Notes
- The role is expected to work in all shifts.
- If required, the candidate should be ready to travel to all plant locations on work priority as per company policy.
- Responsible for ensuring compliance with GLP, Health, Safety, and Environment requirements.
