Quality Control Job at Rubicon Research | MSc Chemistry Graduates Apply Now
Are you looking for an MSc Chemistry job in the pharmaceutical industry? This Quality Control Job opportunity for an Officer (Analyst) role in Satara is ideal for professionals aiming to build strong chemical science careers in pharmaceutical quality laboratories. The position involves analytical testing of raw materials, packaging materials, water samples, in-process materials, and finished products using advanced analytical instruments. Candidates with experience in HPLC, GC, UV, IR, and dissolution testing can enhance their technical expertise while working in a regulated environment following GLP, GDP, and GMP standards. This role offers valuable exposure to pharmaceutical quality systems and helps professionals strengthen their chemical science careers.
About Rubicon Research
The organization is a reputed pharmaceutical manufacturing company committed to delivering high-quality medicines while maintaining strict global regulatory standards. The company focuses on innovation, quality assurance, and advanced analytical testing to ensure the safety and effectiveness of pharmaceutical products. With modern laboratories and experienced professionals, the organization supports employees in building strong chemical science careers through continuous learning and professional development. Working in such an environment allows candidates to gain exposure to international quality systems, regulatory guidelines, and modern analytical
technologies. This commitment to quality and growth makes it an excellent workplace for professionals seeking long-term, excellent opportunities in the pharmaceutical sector.- Job Title: Officer (Analyst)
- Location: Satara
- reqId: 181575
- Department: Quality Control
- Experience: 2 to 5 years
Dosage Form: Solid Oral / Nasal / Liquid
Job Responsibilities / Deliverables
- 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 to 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 & Pre-Requisites
- 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 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.
