OPES Healthcare Hiring Formulation & Development

Opes Healthcare Pvt. Ltd.

Ahmedabad District

On-site

INR 500,000 - 900,000

Full time

14 days+

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Job summary

OPES Healthcare Private Limited invites B.Pharm, M.Pharm professionals for Formulation & Development roles at its Changodar R&D Center in Gujarat. Hands-on exposure to sterile injectables and ophthalmic formulations is preferred, with 2–7 years of relevant experience.

You will drive development, scale-up, technology transfer, and regulatory documentation in a compliance-driven environment focused on quality and patient safety.

Qualifications

B.Pharm, M.Pharm (Pharmaceutics or related disciplines)
2–7 years of relevant experience in pharmaceutical formulation and development
Hands-on exposure to sterile dosage forms such as injectables or ophthalmics
Experience in regulated R&D environments is preferred
Strong understanding of pharmaceutical development principles and regulatory documentation

Responsibilities

Develop and optimize sterile formulations including injectables and ophthalmic products
Plan and execute formulation trials in line with regulatory guidelines
Support scale-up activities and technology transfer to manufacturing units
Prepare, review, and maintain formulation and development documentation
Draft and review protocols, reports, and batch manufacturing records
Ensure compliance with cGMP, GLP and applicable regulatory requirements
Coordinate with QA, QC, Production and Regulatory Affairs teams
Support troubleshooting during development and scale-up
Participate in stability studies and validation activities

Skills

Sterile formulation

Injectables

Ophthalmic formulations

Regulatory documentation

Cross-functional collaboration

Technical communication

Education

B.Pharm, M.Pharm (Pharmaceutics or related)

Job description

B.Pharm, M.Pharm F&D Vacancies – OPES Changodar

OPES Healthcare hiring B.Pharm, M.Pharm professionals for Formulation & Development roles in Changodar. 2–7 years experience.

OPES Healthcare Private Limited is expanding its Research and Development operations and inviting applications from experienced pharmaceutical professionals for Formulation & Development roles at its Changodar R&D Center. This opportunity is ideal for candidates with hands‑on exposure to sterile formulation development who want to work in a compliance-driven R&D environment focused on innovation, quality, and patient safety. Professionals with experience in injectables and ophthalmic formulations will find this role highly rewarding for long‑term career growth in pharmaceutical research and development.

Company Overview

OPES Healthcare Private Limited is a growing pharmaceutical organization focused on the development of high-quality, affordable healthcare solutions. The company operates with a strong emphasis on research-driven product development, regulatory compliance, and robust quality systems. OPES Healthcare’s R&D and manufacturing activities are aligned with global regulatory expectations, ensuring that developed products meet international quality and safety standards.

With dedicated teams in formulation development, quality assurance, quality control, and regulatory affairs, OPES Healthcare provides a collaborative environment where scientific expertise directly contributes to improving patient outcomes. The organization follows cGMP and GLP practices and adheres to regulatory frameworks such as ICH, FDA, and WHO guidelines, making it a reliable and credible employer in the pharmaceutical R&D sector.

Job Role & Responsibilities

Senior Officer / Executive – Formulation & Development

The selected candidate will play a key role in developing and optimizing sterile pharmaceutical formulations. This position is critical to ensuring successful product development, scale-up, and technology transfer from R&D to manufacturing. Key responsibilities include:

Development and optimization of sterile formulations including injectables and ophthalmic products
Planning and execution of formulation trials in line with regulatory guidelines
Supporting scale-up activities and technology transfer to manufacturing units
Preparation, review, and maintenance of formulation and development documentation
Drafting and reviewing protocols, reports, and batch manufacturing records
Ensuring compliance with cGMP, GLP, and applicable regulatory requirements
Working in alignment with ICH, FDA, and WHO guidelines
Coordinating with QA, QC, Production, and Regulatory Affairs teams
Supporting troubleshooting activities during development and scale-up
Participating in stability studies and validation support activities

This role provides hands‑on exposure to the full product development lifecycle, from laboratory formulation to commercial manufacturing readiness.

Eligibility / Qualifications

Educational Qualifications:

B.Pharm, M.Pharm (Pharmaceutics or related disciplines)

Experience Requirements:

2 to 7 years of relevant experience in pharmaceutical formulation and development
Hands‑on exposure to sterile dosage forms such as injectables or ophthalmics
Experience working in regulated R&D environments is preferred

Additional Skills:

Strong understanding of pharmaceutical development principles
Working knowledge of regulatory documentation and compliance
Ability to collaborate with cross‑functional teams
Good communication and technical documentation skills

Location & Salary

Work Location:

R&D Center, Changodar, Ahmedabad, Gujarat

Salary and compensation will be offered as per industry standards and will be commensurate with the candidate’s qualifications, experience, and technical expertise. OPES Healthcare follows structured HR policies and offers performance-based growth opportunities.

Employee Benefits