Officer – Analytical (Analyst) at Rubicon
Rubicon Pharma jobs offer a rare chance for qualified candidates to join a leading organization as an Officer in Analytical Method Validation. This position is based in Pithampur and requires candidates with a background in quality control and relevant experience in analytical methods. Interested individuals should apply before the deadline.
About the Company
The organization is a prominent player in the pharmaceutical industry, focusing on quality control and analytical method validation. With a commitment to maintaining high standards in product quality, the company operates in compliance with GLP, GDP, and GMP regulations, ensuring the safety and efficacy of its products.
Rubicon Pharma Jobs: Job Details
- Location: Indore
- Category: Quality Control
- Req ID: 1795
- Job Type: New
- Department: Analytical Method Validation
- Reporting To: Assistant Manager (P3) / Manager (P4)
- Experience Required: 2–6 years
- Dosage Form Exposure: Solid Oral Dosage Forms
Job Description
In these Rubicon Pharma jobs, the Officer will be responsible for performing physical, chemical, and instrumental analysis related to method validation, verification, and transfer activities. This role requires hands-on experience with various analytical instruments and a strong commitment to compliance with laboratory standards.
Key Responsibilities
- Perform physical, chemical, and instrumental analysis related to method validation, method verification, and method transfer activities.
- Hands-on experience with analytical instruments such as HPLC, GC, UV, IR, and Dissolution apparatus.
- Prepare validation/verification/transfer protocols and detailed technical reports.
- Coordinate with the Analytical Development team in case of deviations or discrepancies observed during validation, verification, or transfer activities.
- Perform calibration of instruments and qualification of working standards as per SOPs.
- Provide support to QC analysis activities whenever required.
- Ensure strict adherence to GLP and Health, Safety & Environment (HSE) guidelines in the laboratory.
- Execute additional tasks assigned by the supervisor or HOD as per business requirements.
- Maintain strong written and verbal communication skills for documentation and coordination.
Eligibility Criteria
- B.Sc. / M.Sc. in Science or B.Pharm / M.Pharm or equivalent qualification.
- Hands-on experience in HPLC / GC / UV / IR / KF / Dissolution techniques.
- Experience working in a GLP, GDP, and GMP-compliant laboratory environment.
- Candidates from USFDA-approved manufacturing sites will be preferred.
- Exposure to Chromeleon 7.2 software will be an added advantage.
- Ability to independently execute analytical deliverables with minimal supervision.
Additional Requirements
- Willingness to work in rotational shifts.
- Flexibility to travel to different plant locations based on business requirements.
- Strong commitment to compliance with GLP, Health, Safety, and Environmental standards.
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This Rubicon Pharma jobs opportunity presents an excellent chance for qualified candidates to advance their careers in the pharmaceutical industry. Interested individuals are encouraged to apply at the earliest to secure their chance for this role.
