Piramal Pharma Hiring Senior Research Associates | M.Sc./M.Pharm | Analytical & Formulation Roles

Apply now for Senior Research Associate roles at Piramal Pharma Solutions in Ahmedabad. Openings in Analytical Development (QA/QC), Formulation Development for M.Sc. & M.Pharm professionals with 2–7 years of experience. Work in a USFDA-compliant facility and advance global healthcare.

💼 Piramal Pharma Solutions Hiring Senior Research Associates – Ahmedabad | Apply Now for QA, QC, Analytical & Formulation Roles

Piramal Pharma Solutions, a global contract development and manufacturing organization (CDMO), is expanding its Formulation Services team in Ahmedabad, Gujarat. If you’re a qualified M.Sc. or M.Pharm professional with 2–7 years of experience, this is your chance to be part of an organization that shapes the future of pharmaceuticals.

With world-class infrastructure, cGMP-compliant labs, and a collaborative work culture, Piramal Pharma Solutions (PPS) is the ideal place for scientists looking to innovate in drug development.

🌐 About Piramal Pharma Solutions

Piramal Pharma Solutions is a globally recognized CDMO with a full spectrum of services for drug discovery, development, and manufacturing. Our Ahmedabad facility is dedicated to Oral Solid Dosage (OSD) forms and supports end-to-end development—from pre-formulation to commercial scale-up.

• Global Reach: Trusted partner for top pharma companies worldwide

• Regulatory Strength: Facilities audited by USFDA, MHRA, and other global agencies

• Compliance: Adheres to strict cGMP, GLP, and GDP norms

• Innovation Focus: Integrates QbD, digital labs, and automation for next-gen pharma solutions

📍 Job Location

• City: Ahmedabad, Gujarat

• Facility: Piramal Pharma Solutions – Formulation Services Unit

📋 Open Positions & Job Descriptions

We are hiring for Senior Research Associate roles in the following departments:

1️⃣ Senior Research Associate – Analytical Development QA

• Vacancies: 1

• Qualifications: M.Sc. or M.Pharm (Full-Time)

• Experience: 4–7 years in analytical quality assurance

Key Responsibilities:

• Monitor and close analytical incidents, deviations, and change controls

• Review method validation, stability data, and clinical batch records

• Lead internal audits, QMS documentation, and SOP creation

• Manage instrument IQ/OQ/PQ, CSV, and Empower software validations

Skills Required:

• In-depth knowledge of cGMP, GLP, GDP, and data integrity

• Strong audit preparedness, documentation, and compliance focus

• Familiarity with digitalized lab systems and automation platforms

2️⃣ Senior Research Associate – Analytical Development QC

• Vacancies: 1

• Qualifications: M.Sc. or M.Pharm (Full-Time)

• Experience: 2–4 years in analytical quality control

Key Responsibilities:

• Perform method validation and verification

• Conduct routine testing for clinical and stability samples

• Maintain and calibrate HPLC, UPLC, and analytical instruments

• Prepare technical reports, COA, STP, and validation protocols

Skills Required:

• Experience in HPLC/UPLC analysis, audit trail review

• Strong command of GLP, GDP, and compliance standards

• Solid analytical documentation and technical writing skills

3️⃣ Senior Research Associate – Analytical Development

• Vacancies: 1

• Qualifications: M.Sc. or M.Pharm (Full-Time)

• Experience: 2–4 years in analytical method development

Key Responsibilities:

• Develop and validate methods for tablets, capsules, and FDCs

• Operate HPLC, UPLC, UV, KF titrators, and dissolution test units

• Perform routine and stability analysis for formulations

• Maintain data and ensure full cGMP compliance

Skills Required:

• Proficient in Assay, RS, CU, Dissolution method development

• Hands-on with advanced analytical tools

• Knowledge of regulatory guidelines and report generation

4️⃣ Senior Research Associate – Formulation Development

• Vacancies: 1

• Qualifications: M.Pharm (Full-Time)

• Experience: 2–4 years in formulation development

Key Responsibilities:

• Develop oral solid dosage forms using QbD

• Handle GMP batch manufacturing for NCEs, generics, and line extensions

• Prepare development reports, tech transfer, and scale-up documentation

• Ensure compliance with documentation practices and data standards

Skills Required:

• Expertise in formulation design, pre-formulation, and process optimization

• Working knowledge of regulatory submission standards

• Excellent cross-functional coordination and report drafting

🎯 Why These Roles Are Important

These Senior Research Associate roles contribute directly to:

• Global drug development pipelines

• Regulatory compliance for clinical and commercial manufacturing

• Innovation in drug delivery and formulation science

• Upholding the highest quality standards in pharmaceutical R&D

As a part of Piramal Pharma Solutions, your work impacts patients worldwide, shaping access to quality and affordable healthcare.

🌟 Benefits of Working at Piramal Pharma Solutions

✅ Competitive Compensation: Market-aligned salaries with additional perks
✅ Work-Life Balance: 5-day work culture with wellness initiatives
✅ Global Exposure: Collaborate with leading pharma companies
✅ Training & Growth: Regular upskilling sessions and promotion tracks
✅ Culture: Diverse, inclusive, and innovation-driven work environment
✅ Technology: Work with automated platforms, data-integrity tools, and compliance software

📬 How to Apply

Send your updated CV with the subject line:
Vacancy – [Mention Role Name]

To:
📧 Kinjal.pal@piramal.com
📧 Prathamesh.shinde2@piramal.com

🔄 Application Process

📢 Applications are reviewed on a rolling basis—apply early for priority consideration.

🏢 About the Ahmedabad Facility

Piramal’s Ahmedabad R&D center is built for Formulation Innovation and Analytical Excellence. The facility offers:

• Dedicated labs for Analytical Development, Formulation R&D, and Quality Assurance

• Modern analytical instruments (HPLC, UPLC, GC, UV, KF, Dissolution)

• State-of-the-art infrastructure compliant with USFDA, MHRA, and cGMP standards

Explore more at:
🔗 Piramal Pharma Solutions – Official Website
🔗 Piramal Careers Portal

🧭 Design Your Destiny with Piramal Pharma Solutions

Join a team where science meets purpose. If you’re passionate about drug innovation, data integrity, and global impact, this is your chance to grow with India’s leading CDMO. As a Senior Research Associate, you’ll be at the heart of formulation and analytical breakthroughs.

📩 Apply Today – Be the Next Scientific Leader in the Making.