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Zydus IPQA Jobs in Ahmedabad – Officer Quality Assurance Vacancy 2026
Published on: September 20, 2026
Zydus Lifesciences is hiring for an Officer – IPQA position at its ZHL Lyophilise Plant, Vatva, Ahmedabad, Gujarat. The role is part of the Quality Assurance department and focuses on in-process quality assurance, equipment qualification, validation activities, CAPA implementation and cGMP compliance.
The vacancy requires B.Pharm or M.Pharm with 2–4 years of experience. The listing specifically mentions hands-on experience in sterile injectable manufacturing plants, making previous exposure to sterile manufacturing particularly relevant for this position.
1. Zydus IPQA Jobs in Ahmedabad – Vacancy Details
| Particular | Details |
|---|---|
| Company | Zydus Lifesciences |
| Position | Officer – IPQA |
| Department | Quality Assurance |
| Location | ZHL Lyophilise Plant, Vatva, Ahmedabad, Gujarat |
| Qualification | B.Pharm / M.Pharm |
| Experience | 2–4 years |
| Zydus Experience | 1–2 years mentioned in listing |
| Relevant Experience | Sterile injectable manufacturing |
| Vacancies | 1 |
| Position Type | Expansion Position – Project |
| Reports To | IPQA Lead |
| Job ID | JOB11126 |
| Division | ZHL Lyophilise Plant QA |
| Updated | September 19, 2026 |
| Employee Type | P-P8-Probationer-HO Executive |
| Official Job Listing / Apply Online | View Zydus IPQA Vacancy |
2. What Does an IPQA Officer Do?
IPQA (In-Process Quality Assurance) focuses on quality oversight during pharmaceutical manufacturing. The work involves monitoring manufacturing activities and ensuring that approved procedures, quality requirements and documentation are followed.
An IPQA professional may work with manufacturing and quality teams on:
- In-process quality checks
- Manufacturing documentation
- Equipment qualification
- Validation activities
- Risk assessments
- CAPA
- cGMP compliance
- Manufacturing-floor activities
For this vacancy, experience in sterile injectable manufacturing is particularly important because it is specifically mentioned in the listing.
3. Key Responsibilities
The responsibilities in the vacancy can be grouped into the following areas:
| Area | What the Role Involves |
|---|---|
| Equipment Qualification | Supporting qualification activities and reviewing related documentation |
| Validation | Participating in validation and process improvement activities |
| Risk Assessment | Approving impact and risk assessment documents |
| Qualification Documents | Working with URS, DQ, FAT, IQ, OQ and PQ documentation |
| Manufacturing | Participating in machine setup and startup activities |
| IPQA | Performing in-process QA during manufacturing, filling and sealing |
| CAPA | Supporting implementation of corrective and preventive actions |
| Compliance | Supporting cGMP compliance within the manufacturing facility |
4. Equipment Qualification and Validation
Equipment qualification is an important part of this position. The vacancy specifically refers to several documents and qualification stages.
| Term | Full Form | Purpose |
|---|---|---|
| URS | User Requirement Specification | Defines the user’s requirements for equipment or a system |
| DQ | Design Qualification | Documents whether the proposed design meets specified requirements |
| FAT | Factory Acceptance Testing | Testing performed at the supplier/manufacturer’s site before delivery |
| IQ | Installation Qualification | Verifies that equipment has been installed correctly |
| OQ | Operational Qualification | Verifies that equipment operates as intended |
| PQ | Performance Qualification | Confirms that the equipment performs consistently under actual or intended operating conditions |
Candidates who have practical experience with these activities should clearly mention the specific qualification or validation work they have handled on their resumes.
5. IPQA During Manufacturing
The selected candidate will perform in-process quality assurance during manufacturing, filling and sealing of products.
This means the role involves interaction with manufacturing activities rather than being limited to documentation work.
Relevant experience may include:
- Monitoring manufacturing operations
- Reviewing batch documentation
- Performing in-process checks
- Monitoring filling and sealing operations
- Supporting machine setup and startup
- Checking compliance with approved procedures
- Recording and reviewing observations
Candidates should describe their actual responsibilities rather than simply writing “worked in QA” on their resume.
6. CAPA, Risk Assessment and cGMP
The position also involves quality-system activities that support manufacturing compliance.
| Area | What Candidates Should Understand |
|---|---|
| CAPA | Corrective and preventive actions used to address problems and prevent recurrence |
| Risk Assessment | Identifying and evaluating potential quality or process risks |
| Impact Assessment | Evaluating the potential effect of a change, event or issue |
| cGMP | Following applicable good manufacturing practices during pharmaceutical operations |
| Documentation | Maintaining accurate and traceable quality records |
Candidates preparing for an interview should be able to explain these concepts using examples from their actual work experience.
7. How to Prepare Your Resume
A generic QA resume may not clearly demonstrate whether your experience matches this particular vacancy.
Where applicable to your actual experience, highlight:
| Skill / Experience | Examples to Mention |
|---|---|
| IPQA | In-process checks, manufacturing-floor QA |
| Sterile Manufacturing | Sterile injectable manufacturing experience |
| Equipment Qualification | IQ, OQ, PQ and related documentation |
| Validation | Process or equipment validation activities |
| CAPA | CAPA implementation or follow-up |
| Risk Assessment | Risk and impact assessment activities |
| Qualification Documents | URS, DQ, FAT, IQ, OQ, PQ |
| Manufacturing Operations | Machine setup, startup, filling and sealing |
| cGMP | GMP compliance and documentation |
Only include skills you have genuinely handled. Technical terms listed on your resume may be discussed in detail during the interview.
8. Who Is This Vacancy Relevant For?
This position is particularly relevant to candidates who already have experience combining QA responsibilities with pharmaceutical manufacturing operations.
Before applying, compare your profile with these key requirements:
- B.Pharm or M.Pharm
- 2–4 years of relevant experience
- Experience in sterile injectable manufacturing
- Practical IPQA exposure
- Familiarity with qualification and validation activities
- Understanding of CAPA and cGMP
- Ability to work with manufacturing and quality documentation
Meeting the degree requirement alone does not establish that a candidate meets the complete experience requirement.
If you are a B.Pharm graduate and want to understand the QA career path in more detail, read our guide on Career in Quality Assurance (QA) After B.Pharm.
9. How to Apply for Zydus IPQA Jobs in Ahmedabad
Candidates interested in the vacancy can check the official Zydus Group careers portal for the current job listing and application instructions.
Official Zydus Careers:
Zydus Group Careers – Apply Online
Search for Officer – IPQA or JOB11126 and follow the application instructions provided by the company.
Recruiter Details
| Contact | Details |
|---|---|
| HR Name | Vinod Prajapati |
| Phone | 6358855193 |
| Vinodg.prajapati@zyduslife.com |
If you contact the recruiter, mention the Officer – IPQA position and briefly state your qualification and relevant experience.
10. Common Mistakes to Avoid
1. Ignoring the Sterile Manufacturing Requirement
The vacancy specifically mentions hands-on experience in sterile injectable manufacturing plants. Candidates should carefully check this requirement before applying.
2. Using a Generic QA Resume
Make your IPQA and manufacturing experience easy to identify. Mention the specific activities you have actually performed.
3. Adding Skills You Cannot Explain
Do not copy technical terms from the vacancy simply to match keywords. You should be able to explain your practical experience with any skill mentioned on your CV.
4. Not Checking the Job ID
Use JOB11126 when checking the vacancy on the Zydus careers portal so that you are looking at the relevant position.
11. Frequently Asked Questions
What position is Zydus Lifesciences hiring for?
The vacancy is for an Officer – IPQA position in the Quality Assurance department.
Where is the position located?
The position is at the ZHL Lyophilise Plant, Vatva, Ahmedabad, Gujarat.
What qualification is required?
The vacancy lists B.Pharm or M.Pharm.
How much experience is required?
The listed requirement is 2–4 years, with hands-on experience in sterile injectable manufacturing plants specifically mentioned.
What is the job ID?
The job ID is JOB11126.
How many vacancies are available?
The supplied listing mentions 1 vacancy.
Who is the listed HR contact?
The supplied listing names Vinod Prajapati as the HR contact.
Phone: 6358855193
Email: Vinodg.prajapati@zyduslife.com
12. Important Note
The vacancy information above is based on the supplied job listing. Candidates should verify the current vacancy status, eligibility and application procedure through the official Zydus careers portal before applying.
PharmaCareerUpdates.com is an independent career-information website and is not affiliated with Zydus Lifesciences.
