Team Member – SIT Job – at Dr. Reddy’s, Apply Today!
Are you passionate about quality assurance and pharmaceutical excellence? Join Dr. Reddy’s SIT Team, where you will oversee investigations, identify root causes, and implement corrective and preventive actions (CAPA). This role offers the opportunity to collaborate with Cross-Functional Teams (CFTs), manage Out of Specification (OOS) cases, and ensure compliance with regulatory standards. Take the next step in your career by contributing to world-class manufacturing processes and regulatory excellence at Dr. Reddy’s.
Roles & Responsibilities:
- You will be responsible for overseeing the investigations of deviations from the outset, collaborating closely with Cross-Functional Team (CFT) members to identify root causes, corrective actions (CA), preventive actions (PA), and preparing comprehensive reports.
- Your role involves active participation in investigating valid OOS (Out of Specification) and other relevant cases, working closely with CFT members to determine root causes, CA, PA, and report writing.
- You will review level Minor (Investigation required), Major and Critical incidents, providing constructive feedback for improvement.
- Your responsibilities include periodically assessing the trending of level deviations, highlighting or escalating key observations, regularly reviewing the DCMS log or SAP OOS log to ensure accurate classification, and utilizing the Rubrics template for crafting investigation reports.
- You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations.
Qualifications for Team Member – SIT Job:
Educational qualification: A Bachelor’s or Master’s degree in a relevant scientific field, such as Chemistry, Biochemistry, Pharmacy, or related discipline
Minimum work experience: 5 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance
Skills & Attributes
Technical Skills for Team Member – SIT Job:
- In-depth knowledge and experience in overseeing investigations, and familiarity with root cause analysis, corrective actions (CA), and preventive actions (PA).
- Expertise in investigating valid OOS and other relevant cases.
- Familiarity with reviewing deviations log and ability to perform classification of data.
- Ability to craft comprehensive investigation reports.
- Experience in providing necessary support for regulatory inspections related to investigations.
- Knowledge of regulatory requirements pertaining to incident investigations.
Behavioural Skills for Team Member – SIT Job:
- Ability to collaborate closely with CFT members.
- An analytical mindset for identifying root causes and developing effective solutions.
- Strong problem-solving skills and attention to detail in reviewing incidents, reports, and trending data and implementing corrective actions.
- Effective communication skills for report writing and escalation of key observations.
- Commitment to ensuring compliance with regulatory requirements in investigations.
- Ability to offer necessary support to the site in readiness for or during regulatory inspections.
Additional Information for Team Member – SIT Job:
About the Department: Global Manufacturing Organization (GMO)
Benefits Offered: At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
Keywords: Job Posting, Team Member, SIT, Dr. Reddy’s, Pharmaceuticals, Investigations, Quality Assurance
