Pharma Quality Control Job at Rubicon | Officer-QC | Apply Now
Looking for a Quality control Job in the pharmaceutical industry? This excellent Pharma Job opportunity for an Officer/Sr. Officer roles in Satara are ideal for candidates with 2–5 years of experience in QC analysis. Candidates with hands-on experience in HPLC, GC, UV, IR, and dissolution testing can build a strong career through this Quality control Job in a reputed pharma organization.
- Job Title: Officer/Sr. Officer
- Location: Satara
- reqId: 205135
About the Company
Rubicon Research Limited is a global pharmaceutical company known for its expertise in innovative drug delivery systems and complex formulations. The company specializes in developing modified-release dosage forms and provides end-to-end solutions, including research, development, and manufacturing for regulated markets like the US and Europe. With strong capabilities in R&D, advanced manufacturing facilities compliant with global standards such as USFDA, and a focus on quality and innovation, Rubicon offers excellent opportunities for professionals to grow in a highly regulated and technology-driven pharma 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 the 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
- Bachelor’s / Master’s Degree in 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 a deliverable task 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.
