Fresher Hiring for Research Associate Formulation Development at Piramal Pharma
Piramal Pharma Solutions (PPS), a global leader in drug development and manufacturing, is currently hiring Research Associates in Formulation Development for its Ahmedabad facility. This is an excellent opportunity for freshers and early-career professionals (0–2 years) who hold a Master’s degree in Pharmaceutics (M.Pharm) and are looking to build a career in formulation R&D.
Whether you’re passionate about new chemical entities, generics, or advanced drug delivery systems, this role places you in a fast-paced and scientifically challenging environment with tremendous learning and growth potential. Fresher Hiring for Research Associate Formulation
About Piramal Pharma Solutions (PPS)
Piramal Pharma Solutions is the CDMO (Contract Development and Manufacturing Organization) arm of Piramal Pharma Ltd., with operations across North America, Europe, and Asia. PPS offers integrated drug discovery, development, and manufacturing services for both APIs and finished dosages. Fresher Hiring for Research Associate Formulation
Renowned for its quality-first approach, innovation-driven strategy, and commitment to global compliance, PPS supports pharmaceutical and biotechnology companies at every stage — from pre-clinical development to commercial supply.
Website: www.piramalpharmasolutions.com
Job Role: Research Associate – Formulation Development
Job Title: Research Associate – Formulation Development
Department: R&D – Formulation Development
Location: Ahmedabad, Gujarat
Experience Required: 0 to 2 years
Educational Qualification: M.Pharm (Pharmaceutics)
Job Type: Full-Time
Application Mode: Online
Key Responsibilities
As a Research Associate in Formulation Development, you will be involved in key R&D activities focused on the development of solid oral dosage forms and technology transfers. Your responsibilities include: Fresher Hiring for Research Associate Formulation
- Formulation Development: Design and optimize solid oral formulations for New Chemical Entities (NCEs), generic products, and line extensions.
- Documentation: Draft and review technical documents, including literature summaries, Master Formula Cards (MFCs), Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), and stability study protocols.
- GMP Batch Execution: Oversee pilot-scale and GMP batch manufacturing and conduct scale-up and process development activities.
- Compliance & Training: Ensure adherence to GMP/GDP guidelines and support training of junior team members on quality and safety procedures.
- Technology Transfer: Lead tech transfer projects from R&D to commercial manufacturing units, ensuring seamless handover and documentation.
- QMS Management: Handle quality management systems, including change controls, deviation handling, standard operating procedures (SOPs), and out-of-specification (OOS) investigations.
- Client Interaction: Participate in client meetings, presentations, and regular updates via emails and reports in collaboration with cross-functional teams.
Required Qualifications and Skills
- Educational Requirement:
M.Pharm (Pharmaceutics) from a reputed institution. - Professional Skills:
- Strong grasp of formulation and process development for oral solid dosage forms (tablets, capsules, granules, etc.).
- Proficiency in handling R&D documentation, including development reports and stability protocols.
- Good understanding of QbD (Quality by Design), DOE (Design of Experiments), and related tools is a plus.
- Regulatory & Quality Knowledge:
- Sound understanding of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices).
- Familiarity with global regulatory guidelines and quality management systems.
- Soft Skills:
- Excellent written and verbal communication skills.
- Team-oriented mindset with a collaborative approach.
- Detail-oriented with strong analytical and problem-solving abilities.
Why Join Piramal Pharma Solutions?
PPS is widely recognized for nurturing talent and fostering a culture of innovation and integrity. Here are the key reasons to consider this opportunity: Fresher Hiring for Research Associate Formulation
- Global Exposure: Work in an international environment serving clients from the US, EU, and other regulated markets.
- Comprehensive R&D Experience: Gain hands-on experience in formulation development, GMP batch execution, and regulatory documentation.
- Structured Growth Path: Opportunities to grow from a Research Associate to a Formulation Scientist or Team Leader in future.
- Modern Infrastructure: Access to state-of-the-art labs, high-end instrumentation, and a quality-driven work culture.
- Ethical Workplace: PPS strictly follows ethical, legal, and environmental standards with a zero-tolerance policy for non-compliance.
Equal Opportunity Commitment
Piramal Group is an Equal Opportunity Employer. It embraces diversity and inclusion and ensures that employment decisions are based solely on qualifications, merit, and business needs — without discrimination based on gender, race, religion, disability, or any other protected category. Fresher Hiring for Research Associate Formulation
How to Apply?
Eligible and interested candidates can apply online by visiting the official careers portal of Piramal Pharma Solutions:
Tip: Make sure your resume highlights relevant skills in formulation development, GMP documentation, and R&D project handling. Tailor your application to showcase your technical strengths and your commitment to quality and compliance. Fresher Hiring for Research Associate Formulation
Final Words
If you’re looking to launch your career or transition into formulation development in a regulated environment, this opening at Piramal Pharma Solutions offers the ideal blend of learning, exposure, and job security. Freshers with a Master’s in Pharmaceutics are encouraged to apply and take advantage of this high-impact opportunity in the pharmaceutical R&D sector. Fresher Hiring for Research Associate Formulation
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