Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
- Vacancy details:
- Department: Associate – Clinical QA
- Qualification: Any Life science graduate
- Salary: ₹Not Disclosed
Job Description: Greetings from Dr. Reddy’s Laboratories Ltd..!!
Important Details :
- Location: Hyderabad
- Post of date:25/10/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Roles & Responsibilities
Develop and maintain training matrix for each job role in clinical development in consultation with Functional Head/Leads and assuring all referenced SOPs and guidance are current and accurate.
Circulate updated training matrix, harmonize and incorporate any changes requested by Functional Head/Leads.
Tracking and coordinating of training for new hires, internal promotions and employee re-joining after long leave.
Prepare training materials and conduct class room trainings on SOP/regulatory guidance/QMS documents/eClinical Tools
Create training courses in Learning Management System (LMS) and assign the courses to relevant job roles. Track and ensure employee are compliant with training needs and escalate the non-compliances to Functional Head/Leads
Assist in the development of new training tools and learning initiatives.
Assist in revision of cross functional documentation and training materials when a process is updated or developed.
Participate in process improvement initiatives and collects appropriate metrics and provide periodic scheduled reports on progress against process improvement objectives.
Responsible for management of Archives, coordinating with Biologics archival team for Sponsor documents and coordinating with third party archival service providers (Vendor) for investigator site specific documents.
Review and approve the Invoices generated by Archival vendors.
Other assigned responsibilities as required.
