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Amneal Junior Executive QA Job in Ahmedabad
Published on: October 5, 2026
Amneal Junior Executive QA Job in Ahmedabad is an opportunity with Amneal Pharmaceuticals for candidates interested in pharmaceutical Quality Assurance. The role mainly involves document control, training records and routine QA compliance, with a focus on GMP, documentation and data integrity.
This opportunity may be relevant for B.Pharm, M.Pharm and M.Sc. candidates from Biotechnology, Microbiology or related backgrounds who are looking to build a career in pharmaceutical Quality Assurance.
Quick note: The official job listing does not mention a last date to apply. Since vacancies can be closed without notice, it is better to check the official listing before applying.
1. Job Details at a Glance
| Particular | Details |
|---|---|
| Company | Amneal Pharmaceuticals |
| Position | Junior Executive – Quality Assurance |
| Location | Ahmedabad, Gujarat |
| Job Type | Full-time |
| Job ID | 9171 |
| Qualification | B.Pharm / M.Pharm / M.Sc. |
| Specialization | Biotechnology, Microbiology or related field |
| Experience | Not specified in the official listing |
| Key Area | Quality Assurance |
The official Amneal India careers listing lists this position under Job ID 9171.
2. Who Can Apply?
According to the listing, candidates with B.Pharm, M.Pharm or M.Sc. qualifications in Biotechnology, Microbiology or a related field can apply.
The job posting does not mention a specific experience requirement. However, this does not automatically mean that the position is only for freshers. Candidates should check the current official listing for the exact requirements before applying.
3. What Will You Do in This Role?
The responsibilities are mainly related to document control, training records and QA compliance.
| Area | What the listing mentions |
|---|---|
| Document Management System (DMS) | Managing controlled documents, reviewing, issuing and archiving documents, maintaining the document cell, controlled storage and access, tracking SOPs, formats and logbooks, and replacing older versions when documents are revised |
| Training Management System (TMS) | Maintaining training matrices, checking training records, supporting new-joiner training documentation and coordinating with teams to close training gaps |
| QA Compliance | Supporting routine compliance activities and working with GMP, GDP, ALCOA+ and documentation requirements |
In simple terms, the role is about making sure that the correct documents are available, older versions are controlled properly, and employee training records are maintained correctly.
This is mainly a systems and compliance-focused QA role. The available listing does not mention laboratory testing.
Skills Mentioned in the Listing
The job highlights areas such as:
- GMP
- Data integrity
- Documentation
- Communication
- Cross-functional coordination
- QA knowledge
Since document control and training records are a major part of the role, candidates should be comfortable discussing basic SOP and document-control practices.
4. What to Revise Before the Interview
The job posting does not provide details about the interview process. However, based on the responsibilities mentioned in the listing, these are some useful topics to revise:
| Topic | What to Know |
|---|---|
| GMP | Basic GMP principles and why they are important in pharmaceutical manufacturing and quality systems. The CDSCO official website can also be used for Indian regulatory information. |
| GDP | Good Documentation Practices, including proper entries and corrections. |
| ALCOA+ | Attributable, Legible, Contemporaneous, Original and Accurate, along with Complete, Consistent, Enduring and Available. |
| Document Control | How SOPs and other controlled documents are issued, revised, distributed, replaced and archived. |
| Training Records | How training matrices and employee training records are maintained. |
| Deviation, CAPA and Change Control | Basic meaning of these terms and their role in a pharmaceutical quality system. |
A Couple of Practical Situations to Think About
If you find a missing entry in a logbook:
Do not fill it in from memory or backdate anything. Follow the applicable documentation procedure and inform the responsible person.
If you find an outdated SOP being used:
The correct approach is to follow the document-control procedure and make sure the current approved version is available.
Useful Reference
If you want to understand data-integrity expectations in more detail, the FDA’s Data Integrity and Compliance With Drug CGMP: Questions and Answers is a useful reference.
These topics are worth revising because the position specifically involves controlled documents, training records, GMP and data integrity.
5. How to Apply
To apply:
- Open the official Amneal careers portal.
- Search for Job ID 9171.
- Read the current job description and submit your application with an updated resume.
Apply here: Junior Executive – Quality Assurance – Amneal Job 9171
More from Amneal: Amneal Pharmaceuticals Careers | Amneal India job search
Resume tip: If you have genuine exposure to GMP, documentation or QA activities, mention it clearly on your resume. Avoid claiming DMS or TMS experience if you have not actually worked with these systems.
Caution: Apply only through the official Amneal portal. Do not pay anyone for a job application or recruitment process.
6. Frequently Asked Questions
Is this a government job?
No. This is a private-sector opportunity with Amneal Pharmaceuticals.
What qualifications are required?
The listing mentions B.Pharm, M.Pharm and M.Sc. in Biotechnology, Microbiology or a related field.
Is this position suitable for freshers?
The available listing does not mention an experience requirement or specifically say that the position is only for freshers. Candidates should check the current official posting for the latest eligibility details.
Is there an application deadline?
No specific last date is mentioned in the available official listing. Since vacancies can close without notice, check the official portal before applying.
Is this a QA or QC job?
It is a Quality Assurance position. The listed work focuses on document control, training records, DMS, TMS and QA compliance. Laboratory testing is not mentioned in the available listing.
What do DMS and TMS mean?
DMS (Document Management System) is used to manage controlled documents such as SOPs, formats and logbooks. TMS (Training Management System) is used to maintain employee training records and training matrices.
What is the Job ID?
The Job ID is 9171.
Where should I apply?
Apply through the official Amneal careers portal and search for Job ID 9171.
7. Related Pharmaceutical Career Articles
If you are also looking at other QA and production opportunities, these articles may be useful:
| Career Topic | Read More |
|---|---|
| QA Career After B.Pharm | Career in Quality Assurance (QA) After B.Pharm |
| IPQA Jobs in Ahmedabad | Zydus IPQA Jobs in Ahmedabad |
| Production Jobs in Ahmedabad | Production Executive Job in Ahmedabad |
| Trainee Production Jobs | Trainee – Production Job at Piramal Pharma |
| B.Pharm Career Options | Career Options After B.Pharm |
Final Thoughts
The Amneal Junior Executive – Quality Assurance role could be a good opportunity for candidates interested in the documentation and compliance side of pharmaceutical QA.
The work is particularly focused on document control, training systems, GMP and data integrity, rather than laboratory testing. Before applying, check Job ID 9171 on the official Amneal careers portal to make sure the vacancy is still open and the current requirements match your profile.
Disclaimer: This article is for information only and is not affiliated with Amneal Pharmaceuticals. Job details can change, so always verify the current vacancy, eligibility and application process on the official Amneal careers portal.
