Aizant Drugs Research Job opportunities for Quality Assurance

Aizant® offers comprehensive drug development solutions as an integrated provider. Founded by seasoned pharmaceutical experts with international experience, we have evolved into a dynamic formulation CDMO and CRO. Our wide-ranging capabilities cater to healthcare firms focused on new molecular entities (NME’s), generics (ANDA’s), and over the counter (OTC’s) products worldwide. We enhance the R&D initiatives of our clients significantly throughout the entire drug development process, from molecule discovery to commercialization and ongoing life cycle management. Acting as a crucial intermediary, we bridge the gap between pharmaceutical companies and the healthcare sector.

Greetings from Aizant Drugs Research!

We are hiring following positions.

Executive-Cleaning Validations(QA-Formulation)

We are looking for experienced candidates to Quality Assurance(Cleaning Validations) team at Hyderabad(Dulapally) location.

Experience: 04-06 Years

Below are the roles and responsibilities of Cleaning Validations:

1. Preparation and review of QA SOPs.
2. Review of other departmental SOPs.
3. Preparation of cleaning validation protocols and reports.
4. Preparation of Process validation protocols and reports
5. Preparation of hold-time study protocols and reports.
6. Preparation and Review of Trending Results of Purified Water Results.
7. Preparation and Review of Trends in Environmental Monitoring Reports.
8. Review of APQRs.
9. Participate in quality risk assessments.
10. Review of instrument and equipment qualification protocols and reports.
11. Participate in the execution of instrument and equipment qualifications.
12. To monitor the progress of cGMP manufacturing area documentation requirements.
13. To support and coordinate the issuance of documents sought by the sponsor or client.

Interested candidates can share their resumes to raghuveera.vutla@aizant.com

Note: Immediate Joiners are more preferable

Executive-Process Validations(QA-Formulations)

We are looking for experienced candidates to Quality Assurance(Process Validations) team at Hyderabad(Dulapally) location.

Experience: 04-06 Years

Below are the roles and responsibilities of Process Validations:

• Preparation and review of QA SOPs.
• Review of other department SOPs.
• Preparation of process validation protocols and reports.
• Preparation of packaging validation protocols and reports.
• Preparation of cleaning validation and verification protocols and reports.
• Preparation of hold-time study protocols and reports.
• To be involved in Zen Vector software updates and issues.
• Management roles and privileges in Zen Vector
• Any other responsibilities assigned by the HOD.

Interested candidates can share their resumes to raghuveera.vutla@aizant.com

Note: Immediate Joiners are more preferable.