CIRO Walk-In Regulatory Affairs, FR&D and Softgel Production

CIRO Pharma Hiring Regulatory Affairs & FR&D Roles

CIRO Pharma hiring 14 vacancies in Regulatory Affairs, FR&D and Softgel Production. B.Pharm, M.Pharm, M.Sc candidates eligible.

CIRO Pharma Private Limited is conducting a walk-in recruitment drive for experienced pharmaceutical professionals at its Telangana facility. The company is hiring for multiple positions in Regulatory Affairs, Formulation Research & Development (FR&D), and Production Softgel departments.

Candidates with relevant experience in regulatory submissions, formulation development, technology transfer, softgel manufacturing, and pharmaceutical production operations can attend the walk-in interview scheduled on 20th June 2026. This hiring drive offers opportunities for Senior Executives, Executives, and Operators seeking career growth in a growing pharmaceutical organization.

Professionals with expertise in USFDA, EMA, Emerging Markets (EM), Rest of World (ROW) regulatory submissions, QbD-based formulation development, softgel manufacturing, and pharmaceutical process development are encouraged to participate.

Primary Keyword: Regulatory Affairs Jobs

Company Overview

CIRO Pharma Private Limited is a pharmaceutical manufacturing company engaged in formulation development, regulatory affairs, research and development, and commercial pharmaceutical manufacturing. The company focuses on delivering quality pharmaceutical products while maintaining compliance with global regulatory standards and Good Manufacturing Practices (GMP).

The organization continues to expand its operations across formulation manufacturing, product development, and international regulatory markets. With increasing focus on regulated market submissions and pharmaceutical innovation, CIRO Pharma provides opportunities for professionals seeking careers in regulatory affairs, pharmaceutical research, formulation development, and manufacturing operations.

Employees gain exposure to international regulatory requirements, formulation science, quality systems, technology transfer projects, and commercial pharmaceutical manufacturing processes.

Job Role & Responsibilities

Regulatory Affairs – Formulations

CIRO Pharma is hiring Regulatory Affairs professionals for multiple international markets.

Senior Executive – US

Experience Required: 7 Years

Number of Positions: 2

Key Responsibilities

• Develop regulatory strategies for US market submissions.
• Prepare and compile regulatory dossiers.
• Manage product lifecycle activities.
• Coordinate electronic submissions and regulatory documentation.
• Support regulatory compliance activities and agency communications.
• Monitor regulatory changes and submission requirements.

Senior Executive – EMA

Experience Required: 7 Years

Number of Positions: 2

Key Responsibilities

• Handle regulatory submissions for European markets.
• Prepare CTD and eCTD dossiers.
• Manage lifecycle maintenance activities.
• Support electronic submission management.
• Coordinate with cross-functional teams for regulatory projects.

Senior Executive – EM/ROW

Experience Required: 5 Years

Number of Positions: 2

Key Responsibilities

• Manage regulatory submissions for Emerging Markets and Rest of World regions.
• Prepare market-specific registration dossiers.
• Support product registrations and renewals.
• Maintain regulatory documentation and compliance records.
• Coordinate lifecycle management activities.

Production – Softgel

Bottle Line Operator

Experience Required: 5 Years

Number of Positions: 2

Key Responsibilities

• Operate bottle line equipment in soft gelatin manufacturing.
• Perform line setup and changeover activities.
• Handle production equipment according to SOP requirements.
• Conduct in-process quality checks.
• Maintain batch records and production documentation.
• Troubleshoot equipment issues and monitor line performance.
• Ensure GMP, safety, and hygiene compliance.

Formulation Research & Development (FR&D)

Executive

Experience Required: 5 Years

Number of Positions: 5

Key Responsibilities

• Perform formulation development using Quality by Design (QbD) principles.
• Execute formulation trials and maintain laboratory notebooks.
• Prepare development, validation, and stability documentation.
• Support technology transfer from laboratory scale to commercial manufacturing.
• Review development reports and manufacturing documents.
• Ensure compliance with regulatory guidelines and industry standards.

Operator

Experience Required: 5–8 Years

Number of Positions: 3

Key Responsibilities

• Operate R&D and pilot-scale pharmaceutical equipment.
• Handle compression machines and coating equipment.
• Support formulation development activities.
• Operate process equipment used in pharmaceutical development.
• Manage packaging equipment during development projects.
• Assist in pilot batch manufacturing activities.

Eligibility / Qualifications

Regulatory Affairs

Preferred educational qualifications include:

• B.Pharm
• M.Pharm
• M.Sc
• Life Sciences Graduates

FR&D Executive

Preferred educational qualifications include:

• B.Pharm
• M.Pharm
• M.Sc Chemistry
• M.Sc Pharmaceutical Chemistry

FR&D Operator

Preferred educational qualifications include:

• Diploma
• B.Pharm
• D.Pharm
• Any relevant technical qualification

Production Softgel Operator

Preferred educational qualifications include:

• Diploma
• D.Pharm
• B.Pharm
• Technical Qualifications related to manufacturing operations

Relevant Education Background

B.Pharm, M.Pharm, D.Pharm, M.Sc Chemistry, M.Sc Organic Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Analytical Chemistry, B.Sc Chemistry, Diploma in Pharmacy, Diploma in Mechanical Engineering, Diploma in Production Technology, Life Sciences Graduates.

Location & Salary

Location: Karakapatla, Siddipet, Telangana

Approximate Salary: ₹4.5 LPA – ₹15 LPA

Why Join CIRO Pharma?

The pharmaceutical industry continues to witness strong demand for professionals in Regulatory Affairs, Formulation Development, and Manufacturing Operations. Companies serving regulated and emerging markets require skilled professionals capable of managing submissions, developing formulations, and supporting commercial manufacturing activities.

Key Benefits

• Opportunities in International Regulatory Affairs
• Exposure to USFDA, EMA, EM and ROW Markets
• Career Growth in Pharmaceutical Development
• Hands-On Experience in QbD-Based Formulation Development
• Exposure to Technology Transfer Projects
• Work in a Growing Pharmaceutical Manufacturing Organization
• Opportunities Across R&D and Commercial Manufacturing Functions

Professionals seeking careers in regulatory strategy, pharmaceutical development, dossier preparation, formulation research, and softgel manufacturing can benefit from this recruitment opportunity.

Application Process

Eligible candidates can directly attend the walk-in interview at the venue mentioned below.

Walk-In Interview Details

Date: 20th June 2026 (Saturday)

Time: 10:00 AM Onwards

Interview Venue

CIRO Pharma Private Limited
Plot No. 28
Biotech Park Phase III
Karakapatla
Markook Mandal
Siddipet District
Telangana – 502281

Documents Required

Candidates should carry:

• Updated Resume
• Educational Certificates
• Experience Certificates
• Latest Salary Documents
• Government ID Proof
• Passport Size Photographs

Candidates are advised to reach the venue early for registration and document verification.

Frequently Asked Questions (FAQs)

1. Which departments are hiring at CIRO Pharma?

The company is hiring for Regulatory Affairs, Formulation Research & Development (FR&D), and Production Softgel departments.

2. How many Regulatory Affairs vacancies are available?

A total of 6 positions are available across US, EMA, and EM/ROW regulatory affairs functions.

3. What is the experience requirement for FR&D Executive positions?

Candidates should have approximately 5 years of relevant formulation development experience.

4. What skills are preferred for Regulatory Affairs roles?

Experience in regulatory strategy, dossier preparation, lifecycle management, and electronic submission management is preferred.

5. What experience is required for Production Softgel positions?

Bottle Line Operators should have around 5 years of experience in soft gelatin manufacturing and bottle line operations.

6. What is the work location after selection?

Selected candidates will work at CIRO Pharma’s facility in Karakapatla, Siddipet, Telangana.

Summary

Category	Details
Company	CIRO Pharma Private Limited
Department Vacancies	Regulatory Affairs (US, EMA, EM/ROW), FR&D Executive, FR&D Operator, Production Softgel Bottle Line Operator
Qualification	B.Pharm, M.Pharm, M.Sc, D.Pharm, Diploma, Life Sciences
Experience	5–8 Years
Location	Karakapatla, Siddipet, Telangana