Aspiro Pharma Specialities Private Limited, a unit of the Hetero Group, is conducting a walk-in interview on 30 October 2026 for experienced pharmaceutical professionals at its injectable manufacturing facility in Karkapatla, Telangana. The recruitment drive includes opportunities in Batch Release, Media Fill, Cleaning and Process Validation, Quality Management Systems (QMS), IPQA, and Documentation. Candidates with B.Pharm or M.Pharm qualifications and relevant pharmaceutical industry experience can attend the interview. A joining bonus is also advertised for immediate joiners, subject to the company’s applicable terms.
Aspiro Pharma Walk-in Interview 2026 – Job Overview
| Particulars | Details |
|---|---|
| Company Name | Aspiro Pharma Specialities Private Limited |
| Group | Hetero Group |
| Recruitment Type | Walk-in Interview |
| Number of Vacancies | Not specified |
| Job Location | Karkapatla, Markook Mandal, Siddipet District, Telangana |
| Interview Date | 30 October 2026 |
| Interview Day | Friday |
| Interview Timing | 9:00 AM – 4:00 PM |
| Qualification | B.Pharm / M.Pharm |
| Experience | 2–10 years, depending on the position |
| Departments | Batch Release, Media Fill, Validation, QMS, IPQA, Documentation |
| Salary | Not disclosed |
| Joining Bonus | Advertised for immediate joiners; terms not specified |
| Application Email | mahesh.e@aspiropharma.com |
| Employment Type | Not specified in the poster |
About Aspiro Pharma Specialities Private Limited
Aspiro Pharma Specialities Private Limited, a unit of the Hetero Group, operates in the pharmaceutical sector and has an injectable manufacturing facility at Karkapatla Village, Markook Mandal, Siddipet District, Telangana.
The company is inviting experienced professionals for several quality assurance and pharmaceutical manufacturing support functions. The positions cover batch release, media fill operations, cleaning validation, process validation, quality management systems, in-process quality assurance, and documentation.
Available Positions and Eligibility Criteria
The recruitment poster lists six positions for candidates with B.Pharm or M.Pharm qualifications. Experience requirements differ by role.
| Position | Qualification | Experience |
|---|---|---|
| Senior Officer / Executive – Batch Release | B.Pharm / M.Pharm | 4–6 years |
| Senior Officer / Executive – Media Fill | B.Pharm / M.Pharm | 4–6 years |
| Executive / Senior Executive – CVPV / APQR | B.Pharm / M.Pharm | 5–10 years |
| Senior Executive – QMS | B.Pharm / M.Pharm | 5–10 years |
| Executive / Senior Executive – IPQA | B.Pharm / M.Pharm | 5–10 years |
| Officer – Documentation | B.Pharm / M.Pharm | 2–4 years |
1. Senior Officer / Executive – Batch Release
Qualification: B.Pharm / M.Pharm
Experience: 4–6 years
Key Responsibilities
- Review and release batch records.
- Manage deviations and support corrective and preventive actions (CAPA).
- Handle change control activities.
- Review standard operating procedures (SOPs).
- Ensure compliance with current Good Manufacturing Practices (cGMP).
- Support compliance with applicable regulatory requirements.
Candidates should have relevant pharmaceutical quality experience and an understanding of batch documentation and release procedures.
2. Senior Officer / Executive – Media Fill
Qualification: B.Pharm / M.Pharm
Experience: 4–6 years
Key Responsibilities
- Support media fill operations in injectable manufacturing.
- Follow aseptic practices and applicable procedures.
- Review batch records related to media fill activities.
- Perform trend data analysis.
- Ensure compliance with cGMP requirements.
Candidates with experience in sterile manufacturing, aseptic processing, and media fill activities may be suitable for this role.
3. Executive / Senior Executive – CVPV / APQR
Qualification: B.Pharm / M.Pharm
Experience: 5–10 years
Key Responsibilities
- Review and analyze cleaning validation activities.
- Support process validation and requalification.
- Work on Annual Product Quality Review (APQR) documentation.
- Handle deviations and CAPA-related activities.
- Maintain validation documentation.
- Support regulatory compliance and quality requirements.
Candidates should have relevant experience in pharmaceutical validation, quality documentation, and compliance processes.
4. Senior Executive – Quality Management Systems (QMS)
Qualification: B.Pharm / M.Pharm
Experience: 5–10 years
Key Responsibilities
- Maintain and improve the Quality Management System (QMS).
- Review and maintain SOPs and quality documentation.
- Handle CAPA and change control activities.
- Support internal and external audits.
- Coordinate regulatory compliance activities.
- Ensure effective implementation of quality systems and continuous improvement initiatives.
Candidates with pharmaceutical QMS experience and knowledge of quality systems are encouraged to apply.
5. Executive / Senior Executive – IPQA
Qualification: B.Pharm / M.Pharm
Experience: 5–10 years
Key Responsibilities
- Conduct in-process quality checks.
- Monitor manufacturing activities and product quality.
- Review batch manufacturing and batch packing records (BMR/BPR).
- Perform line clearance and process monitoring.
- Handle out-of-specification (OOS) and out-of-trend (OOT) investigations.
- Support deviation investigations and quality documentation.
- Ensure cGMP compliance and data integrity.
Candidates should have relevant experience in pharmaceutical manufacturing quality assurance and in-process quality control activities.
6. Officer – Documentation
Qualification: B.Pharm / M.Pharm
Experience: 2–4 years
Key Responsibilities
- Prepare, review, and maintain SOPs.
- Maintain batch records, labels, and quality documents.
- Support documentation and regulatory filing activities.
- Ensure data accuracy and completeness.
- Follow up on documentation requirements and closure timelines.
- Maintain records according to established procedures and quality standards.
Candidates with experience in pharmaceutical documentation and quality records may be suitable for this position.
Skills Required for Aspiro Pharma Jobs
Candidates applying for the above positions should have relevant pharmaceutical industry knowledge and experience in their respective functions.
Important skills may include:
- Pharmaceutical quality assurance and quality control.
- cGMP and regulatory compliance.
- Batch record review and release.
- Media fill and aseptic processing.
- Cleaning and process validation.
- Annual Product Quality Review (APQR).
- Quality Management Systems (QMS).
- In-process quality assurance (IPQA).
- Deviation management and CAPA.
- Change control and SOP management.
- Documentation and data integrity.
- Audit support and quality improvement.
The specific technical requirements will depend on the position applied for.
Salary and Joining Bonus
The recruitment poster does not disclose the salary range for these positions. It advertises a joining bonus for immediate joiners, but the amount, eligibility conditions, and payment terms are not specified.
Candidates should confirm the following details with the recruitment team:
- Offered CTC and salary structure.
- Joining bonus amount and eligibility.
- Notice period requirements.
- Shift timings and work schedule.
- Employment terms and benefits.
Aspiro Pharma Walk-in Interview Date, Time and Venue
| Particulars | Details |
|---|---|
| Walk-in Date | Friday, 30 October 2026 |
| Interview Timing | 9:00 AM – 4:00 PM |
| Company | Aspiro Pharma Specialities Private Limited |
| Facility | Injectable Manufacturing Facility |
| Plot Details | Plot No. S-1, S-6 & S-2B, Survey No. 321 & 284 |
| Location | Biotech Park Phase-III, Karkapatla Village |
| Mandal | Markook Mandal |
| District | Siddipet District, Telangana |
| Email for CV Submission | mahesh.e@aspiropharma.com |
Candidates should plan their travel in advance and carry an updated resume with relevant qualifications and experience details.
Documents to Carry for the Walk-in Interview
Candidates should prepare the following documents:
- Updated resume or CV.
- Educational certificates and mark sheets.
- Valid identity proof.
- Recent passport-size photographs.
- Previous employment and experience certificates.
- Relevant training certificates, if applicable.
- Documents supporting experience in pharmaceutical quality functions.
Candidates should confirm with the recruitment team if any additional documents are required.
How to Apply for Aspiro Pharma Walk-in Jobs
Eligible candidates can attend the walk-in interview on 30 October 2026, between 9:00 AM and 4:00 PM, at the Aspiro Pharma Specialities facility in Karkapatla, Telangana.
Candidates who cannot attend the drive can share their CV through the email address provided in the recruitment poster.
Email: mahesh.e@aspiropharma.com
When applying by email, mention the position name in the subject line, such as “Application – Senior Executive QMS” or “Application – IPQA”. Include your qualification, relevant experience, current location, notice period, and contact details in the resume.
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