Morepen Proprietary Drug Research has announced new career opportunities for experienced pharmaceutical professionals across Formulation R&D, API R&D, Research Chemistry, and Quality Assurance. The recruitment drive is aimed at candidates with strong scientific expertise, regulated-market exposure, pharmaceutical development experience, and leadership capabilities.

Professionals holding M.Pharm, M.Sc., or Ph.D. qualifications with relevant industry experience can apply for these positions. Candidates interested in advancing their careers in pharmaceutical research, drug development, analytical quality assurance, and API development should review the eligibility requirements before submitting their applications.

Morepen Recruitment – Job Overview

Particulars Details

Company

Morepen Proprietary Drug Research

Industry

Pharmaceutical Research & Development

Positions

Senior Formulation Scientist, Principal Scientist – API R&D, Sr. Research Chemist, QA Executive

Departments

Formulation R&D, API R&D, Research Chemistry, QA/DQA

Qualifications

M.Pharm, M.Sc. Organic Chemistry, Ph.D. in Pharmaceutics/Chemistry

Experience

3–18 Years, depending on the position

Job Location

Not mentioned in the recruitment advertisement

Application Mode

Email

Email Address

jobs@morepenpdr.com

Contact Number

6302451459

About Morepen Proprietary Drug Research

Morepen Proprietary Drug Research focuses on discovering, developing, and delivering high-quality medicines for global markets. The organization emphasizes innovation-driven pharmaceutical research, quality-focused operations, collaboration, and impactful drug development.

The current recruitment initiative offers opportunities for experienced scientists and quality professionals with expertise in formulation development, API research, regulated-market filings, Quality by Design (QbD), Design of Experiments (DoE), technology transfer, process development, digital chemistry, and AI/ML applications.

Available Positions, Qualifications, and Experience

1. Senior Formulation Scientist

Qualification and Experience:

M.Pharm candidates should have 8–12 years of relevant experience, while Ph.D. candidates in Pharmaceutics should have 5–10 years of experience.

Key Skills and Responsibilities:

Candidates should possess expertise in Formulation R&D, particularly Oral Solid Dosage (OSD) forms and topical formulations. Experience with injectable formulations will be preferred.

Applicants should have experience in ANDA development and regulatory filings for markets regulated by the USFDA, European Union, and Rest of the World (RoW).

Strong knowledge of QbD, DoE, digital formulation technologies, and AI/ML applications is required. Candidates should also possess hands-on experience in technology transfer, scale-up activities, and process development.

Knowledge of USP, ICH, and cGMP guidelines, along with strong leadership, project management, and communication skills, is essential.

2. Principal Scientist – API R&D

Qualification and Experience:

M.Sc. in Organic Chemistry with 12–18 years of experience, or Ph.D. in Chemistry with 10–15 years of experience.

Key Skills and Responsibilities:

Applicants should have extensive experience in API R&D and at least 10 DMF filings. Experience in CIP, Oncology, and Non-Oncology API development for USFDA, EU, and RoW regulated markets is required.

Candidates should have an in-depth understanding and practical implementation experience in QbD and DoE for at least three DMF filings.

The position requires experience in managing multiple teams, designing project timelines, and implementing development strategies according to ICH requirements and market needs.

Exposure to digital chemistry and AI/ML applications in API R&D is desirable. Strong verbal and written business communication skills are also required.

3. Sr. Research Chemist

Qualification and Experience:

M.Sc. in Organic Chemistry with 8–12 years of experience, or Ph.D. in Chemistry with 5–10 years of experience.

Key Skills and Responsibilities:

Candidates should have expertise in API R&D, process development, scale-up, technology transfer, PDR, and DMF documentation.

Hands-on experience with QbD, DoE, ICH guidelines, and pharmaceutical troubleshooting is required.

Applicants should possess experience in team mentoring, cross-functional coordination, and timely project execution.

Exposure to digital chemistry and AI/ML technologies, combined with strong analytical and communication skills, will be advantageous.

4. QA Executive

Qualification and Experience:

M.Sc. with 3–6 years of experience in QA/DQA. The advertisement additionally specifies 4+ years of experience in Analytical DQA/API DQA within a regulated pharmaceutical environment.

Key Skills and Responsibilities:

Candidates should have practical experience with Phase Gate Systems, Project Trackers, Electronic Laboratory Notebooks (ELN), QbD, DoE, SOPs, and Stability Programs.

Applicants should have hands-on exposure to instrument qualification, analytical method and process validation, calibration, change control, deviations, CAPA, and risk assessment.

Strong understanding of GMP, GDP, plant operations, and regulatory compliance requirements for USFDA, EU, and ICH-regulated environments is essential.

Excellent documentation and communication skills are also required.

How to Apply for Morepen Recruitment

Interested and eligible candidates should prepare an updated resume highlighting their educational qualifications, total pharmaceutical industry experience, relevant R&D or QA expertise, regulatory-market exposure, major projects, DMF/ANDA filing experience, and current employment details.

Candidates can submit their applications through the email address provided in the official recruitment advertisement.

Application Email: jobs@morepenpdr.com

Contact Number: 6302451459

Applicants should use a clear email subject line, such as “Application for Senior Formulation Scientist – Candidate Name”, and attach an updated CV in PDF format.

Important Instructions for Applicants

Candidates should carefully verify that their qualifications and experience match the position requirements before applying. Mention relevant regulated-market exposure, technology transfer projects, ANDA or DMF filings, QbD/DoE experience, validation activities, and team management responsibilities clearly in the resume.

The recruitment advertisement does not specify the job location or application deadline. Applicants may contact the company using the official details provided in the advertisement for additional information.

Why Consider Morepen Proprietary Drug Research Careers?

The available positions provide experienced pharmaceutical professionals with opportunities to work in drug development, API research, formulation development, quality assurance, regulated-market projects, digital pharmaceutical technologies, and AI/ML-enabled research.

Professionals seeking senior scientific, technical, and quality roles in pharmaceutical research and development can consider applying if they meet the required qualifications and industry experience.

5 Technical FAQs for Morepen Recruitment

1. What is the role of QbD and DoE in pharmaceutical R&D?

Quality by Design (QbD) is a systematic approach to pharmaceutical development that focuses on predefined product objectives, scientific understanding, and process control. Design of Experiments (DoE) is a statistical methodology used to evaluate the effects of multiple process variables and optimize formulation or API development efficiently.

2. What is the difference between an ANDA and a DMF?

An Abbreviated New Drug Application (ANDA) is submitted to regulatory authorities such as the USFDA to obtain approval for marketing a generic drug product. A Drug Master File (DMF) contains confidential technical information about an API, manufacturing process, facility, or material that supports regulatory submissions.

3. Why is technology transfer important in pharmaceutical manufacturing?

Technology transfer ensures that a formulation or API manufacturing process developed at the laboratory or pilot scale can be successfully reproduced at the commercial manufacturing site. It includes transferring process parameters, analytical methods, equipment requirements, specifications, and technical knowledge while maintaining product quality and regulatory compliance.

4. What are CAPA, deviations, and change control in pharmaceutical Quality Assurance?

A deviation is a departure from an approved procedure or expected result. CAPA, or Corrective and Preventive Action, identifies root causes and establishes actions to correct existing problems and prevent recurrence. Change control is a documented system used to evaluate, approve, implement, and monitor changes that could affect product quality, processes, equipment, facilities, or regulatory compliance.

5. What knowledge should candidates have about ICH and cGMP guidelines?

Candidates should understand ICH guidelines related to pharmaceutical quality, stability, impurities, validation, risk management, and drug development. Knowledge of cGMP requirements is essential for maintaining controlled manufacturing processes, proper documentation, data integrity, validated systems, trained personnel, and consistent product quality.