Team Member- DQA
Aurigene Pharmaceutical Services · Hyderabad · onsite · Posted 36d ago
Undisclosed4–8 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Roles and Responsibilities
- Conduct analytical testing, stability studies, and method validation for API samples using various instruments such as HPLC, GC, UV spectrophotometer, etc.
- Prepare protocols and SOPs related to QbD activities including Change Control Management.
- Ensure compliance with regulatory requirements by reviewing documents like BPR's, SOP's, Method Transfer Protocols, Method Transfer Report, etc.
- Collaborate with cross-functional teams to resolve issues related to documentation and review of documents.
- Maintain accurate records of all experiments performed in the lab.
Desired Candidate Profile
- MS/M.Sc(Science) degree in Chemistry or equivalent qualification.
- 4-8 years of experience in DQA team handling analytical methods development & validation.
- Strong knowledge of ELN (Electronic Lab Notebook) Review process.
- Experience with CDMO DQA operations is desirable.
Sourced from naukri
Skills
Analytical& process developmentCDMO DQAELN (Electronic Lab Notebook) ReviewdoeqbdChange Control ManagementDocumentation ReviewDevelopment Quality Assurance
About Aurigene Pharmaceutical Services

Aurigene Pharmaceutical Services
Pharma
467
employees
2020
6 years old
Bangalore, Karnataka
India
₹7.9L PA avg
Avg at Aurigene Pharmaceutical Services
About
Aurigene Pharmaceutical Services is a leading contract research, development and manufacturing organization(CDMO) providing end-to-end solutions to pharma companies worldwide
Industries
Pharma
Employee ratings
0 reviews
4.2/ 5
Employees rate it well for
Overall Company42Company Culture41
Find them on