Associate Job at Rubicon Research | BPharm Graduates Apply Now
Rubicon Research is hiring an Associate for its Analytical Development II department at the R&D center in Thane, Maharashtra. This Associate Job is a strategic opportunity for B. Pharm or B. Sc. graduates with 1–4 years of experience to manage Reference and Impurity Standards. The successful candidate will ensure that the laboratory maintains high standards of GMP/GLP compliance and data integrity to support the development of oral and nasal formulations for global markets.
- Job Position: Associate
- Location: Thane
- ReqId: 149724
About The Company
Rubicon Research is a world-class specialty pharmaceutical company focused on developing high-quality, innovative drug products. With a strong R&D presence in Thane and manufacturing facilities that are USFDA, MHRA, and ANVISA approved, Rubicon specializes in complex generics and novel drug delivery systems. The organization is driven by a culture of innovation and excellence, supporting a diverse portfolio that ranges from oral solids and liquids to specialized nasal delivery products.
Job Description
Purpose: The candidate shall have the role of management of Reference standards and Impurity standards in the analytical development laboratory to support pharmaceutical formulation development, i.e., Solid/ Oral Liquid and Nasal products.
Dosage Form: Solid Oral / Liquid orals/ Suspensions/Injections/Nasal Sprays
Job Responsibilities / Deliverables
- Standard management.
- To record the incoming working standards, impurity standards entries, and reconciliation of the same.
- Raise the purchase request for the standards in SAP and do the respective follow-up until the standards are received.
- Daily recording ofthe pH of water in the AD department.
- Daily monitoring of the temperature and Humidity of the AD Lab & GC MS Lab.
- Operation of the AD / AMV pharma refrigerator.
- Follow GMP / GLP practices.
- Follow laboratory safety practices.
- Follow the system / operational SOPs.
- Ensure data integrity and accuracy of supporting data.
- Adherence to quality systems and lab practices to ensure compliance with internal/external audits.
Qualifications & Pre-Requisites:
- B. Pharm/B. Sc is required for the BPharm Job
- Knowledge of standard and impurity management.
- Exposure to USFDA/MHRA Audits will be an added advantage.
- Years of Experience: 1-4 years
Additional Notes
- The candidate is expected to work in all shifts.
- The candidate is expected to visit external sites as per project requirements.
