CiRO Pharma Private Limited has announced a Walk-In Interview Drive for experienced pharmaceutical professionals seeking career growth in Regulatory Affairs, Production (Softgel), and Formulation Research & Development (FRD). The recruitment drive offers multiple openings across key functions that play a critical role in pharmaceutical product development, regulatory compliance, and manufacturing excellence.

This hiring initiative presents an excellent opportunity for candidates with relevant experience to join a growing pharmaceutical organization and contribute to global regulatory submissions, softgel manufacturing operations, and innovative formulation development.

About the Hiring Drive

CiRO Pharma is looking for qualified professionals with experience ranging from 5 to 8 years in specialized pharmaceutical domains. The company is hiring for positions in:

Regulatory Affairs – Formulations

Production – Softgel

Formulation Research & Development (FRD)

Candidates with strong technical expertise, GMP knowledge, and regulatory understanding are encouraged to attend the walk-in interview.

Open Positions

1. Regulatory Affairs – Formulations

Senior Executive – US Market

Experience: 7 Years

Open Positions: 2

Key Responsibilities:

Regulatory strategy and lifecycle management

Dossier preparation and compilation

Electronic submission management

Coordination with regulatory authorities

Senior Executive – EMA Market

Experience: 7 Years

Open Positions: 2

Key Responsibilities:

Preparation of CTD/eCTD dossiers

Regulatory compliance for European submissions

Product lifecycle management

Variation and renewal submissions

Senior Executive – EM/ROW Markets

Experience: 5 Years

Open Positions: 2

Key Responsibilities:

Regulatory submissions for emerging and rest-of-world markets

Dossier compilation and maintenance

Electronic submission management

Regulatory strategy implementation

2. Production – Softgel

Bottle Line Operator

Experience: 5 Years

Open Positions: 2

Key Responsibilities:

Softgel bottle line operations

Equipment setup and changeovers

In-process quality checks

GMP and SOP compliance

Production documentation and batch record maintenance

Equipment troubleshooting and routine monitoring

3. Formulation Research & Development (FRD)

Executive

Experience: 5 Years

Open Positions: 5

Key Responsibilities:

Formulation development using QbD principles

Execution of formulation trials

Preparation of development and validation documents

Stability study support

Technology transfer from laboratory to commercial scale

Regulatory compliance during development activities

Operator

Experience: 5–8 Years

Open Positions: 3

Key Responsibilities:

Operation of pilot-scale and R&D equipment

Handling compression and coating machines

Packaging equipment operation

Support for formulation development activities

Walk-In Interview Details

Date: 20th June 2026 (Saturday)

Time: 10:00 AM Onwards

Venue

CiRO Pharma Private Limited

Plot No. 28, Biotech Park Phase III,

Karakapatla, Markook Mandal,

Siddipet, Telangana – 502281

Why Consider This Opportunity?

Exposure to global regulatory markets including US, EMA, and ROW regions

Opportunities in research, development, and commercial manufacturing

Hands-on experience with advanced pharmaceutical technologies

Growth-oriented work environment

Multiple openings across critical pharmaceutical functions

Professionals with strong technical expertise, regulatory knowledge, and manufacturing experience can leverage this opportunity to advance their careers within a dynamic pharmaceutical organization.

Technical FAQs

1. What is the importance of eCTD submissions in Regulatory Affairs?

The Electronic Common Technical Document (eCTD) is the global standard format for regulatory submissions. It allows efficient review, lifecycle management, and electronic communication with regulatory agencies such as the US FDA and EMA.

2. What is Quality by Design (QbD) in formulation development?

QbD is a systematic approach to pharmaceutical development that emphasizes predefined objectives, risk assessment, process understanding, and control strategies to ensure consistent product quality.

3. Why are in-process quality checks critical in softgel manufacturing?

In-process checks help monitor critical quality attributes such as fill weight, capsule integrity, moisture content, and appearance, ensuring compliance with GMP requirements and product specifications.

4. What is technology transfer in pharmaceutical R&D?

Technology transfer is the process of moving a product or manufacturing process from the development stage to commercial production while maintaining product quality, efficacy, and regulatory compliance.

5. What are the major regulatory documents required for formulation product registration?

Key documents include the Common Technical Document (CTD), manufacturing process validation reports, stability data, analytical method validation reports, specifications, and GMP compliance documentation.