Associate Scientist

Kemin Industries South Asia Pvt Ltd.; Chennai; Vor Ort; INR 1.200.000 - 2.000.000; Vollzeit

Zusammenfassung

Kemin Industries South Asia Pvt Ltd. in Chennai seeks an experienced scientist with a minimum of 5 years in pharmaceutical formulation development to lead development, optimization, and stability assessments of diverse dosage forms, ensuring GMP compliance and regulatory alignment.

The role requires hands-on experience with liquids, semi-solids, powders, tablets, and sterile formulations, plus capability to evaluate formulations against pharmacopeial standards and oversee technology transfer

Qualifikationen

• Postgraduate qualification in Pharmaceutical Sciences (M.Pharm or equivalent).
• Minimum 5 years hands-on experience in pharmaceutical formulation development.
• Exposure to multiple dosage forms: liquids, semi-solids, powders, tablets, and sterile formulations.
• Strong understanding of GMP and regulatory requirements.
• Ability to independently evaluate formulation quality against regulatory/pharmacopoeial standards.
• Experience in scale-up batches and technology transfer is preferred.

Aufgaben

• Develop and optimize formulations across dosage forms including liquids, semi-solids, powders, tablets, and sterile products.
• Plan, conduct, and evaluate formulation stability studies.
• Ensure compliance with the Drugs and Cosmetics Act, regulatory requirements, and pharmacopoeial standards.
• Prepare development reports, trial records, and maintain GMP documentation.
• Support pilot-scale and commercial-scale manufacturing and technology transfer.

Kenntnisse

Formulation development

Stability assessment

Regulatory knowledge

GMP compliance

Documentation

Analytical thinking

Problem solving

English communication

Ausbildung

M.Pharm or equivalent

Jobbeschreibung

Postgraduate Degree in Pharmaceutical Sciences (M.Pharm or equivalent)

ROLE SUMMARY

• We are seeking an experienced and competent scientist with a minimum of 5 years of relevant experience in pharmaceutical formulation development, evaluation, and stability assessment.
• The candidate should have hands‑on experience in developing a diverse range of pharmaceutical dosage forms, including liquid, semi‑solid, orals, powders, and sterile formulations. The ideal candidate should possess sound technical knowledge, GMP-compliant pharmaceutical manufacturing, a strong understanding of regulatory requirements, and the ability to independently evaluate and qualify formulations in accordance with applicable pharmacopoeial and regulatory standards.
• Experience in scale‑up batches, technology transfer, and will be an added advantage.

KEY RESPONSIBILITIES

1. Formulation Development and Optimization

• Develop and optimize pharmaceutical formulations across various dosage forms, including:
• Liquid formulations
• Semi‑solid formulations such as ointments, creams, and gels
• Powders
• Tablets and other solid oral dosage forms
• Sterile pharmaceutical formulations.
• Conduct formulation trials, evaluate performance, and optimize formulations to meet quality targets. Resolve formulation‑related technical challenges.
• Plan, conduct, and evaluate formulation stability studies.
• Apply knowledge of the Drugs and Cosmetics Act, applicable Rules, and pharmacopoeial standards; interpret monographs and regulatory specifications; and independently assess and recommend formulation acceptance against regulatory and pharmacopoeial criteria.

2. Manufacturing, Documentation, and Research Support

• Participate in pilot‑scale and commercial‑scale batch manufacturing.
• Prepare and review formulation development reports, trial records, stability reports, and technical documentation. Ensure Good Manufacturing Practices (GMP) compliance and maintain scientific documentation per quality system requirements.
• Carry out experiments as per the direction of the research manager by following the Product Innovation Process (PIP) of Kemin.
• Carry out literature search and identify appropriate methods for conducting research.
• Contribute to writing research reports and presentations.
• Writing of technical articles based on the research finding on a timely basis for internal and external publications.
• Gain knowledge about animal nutrition and health and submit ideas for new product development.

QUALIFICATIONS AND EXPERIENCE

• Must have: Postgraduate qualification in Pharmaceutical Sciences (M.Pharm or equivalent).
• Minimum 5 years of hands‑on experience in pharmaceutical formulation development.
• Practical exposure to multiple dosage forms, particularly liquids, semi‑solids, powders, tablets, and sterile formulations.
• Strong understanding of formulation development principles and stability assessment.
• Knowledge of the Drugs and Cosmetics Act, applicable regulatory requirements, pharmacopoeial standards, and monographs.
• Good understanding of GMP and pharmaceutical quality requirements.
• Ability to independently evaluate formulation quality and determine compliance with applicable regulatory and pharmacopoeial standards.
• Strong analytical thinking, problem‑solving, and decision‑making abilities.
• Excellent written and verbal communication skills in English.
• Ability to work independently as well as collaboratively within a multidisciplinary team.

PREFERRED EXPERIENCE

• Experience in scale‑up batches and technology transfer.
• Exposure to commercial manufacturing and troubleshooting of formulation‑related issues.
• Experience working in a GMP‑regulated pharmaceutical manufacturing or R&D environment.

CORE COMPETENCIES

Competency Area

Scientific and Technical

Pharmaceutical formulation development; stability assessment; regulatory and pharmacopoeial knowledge; GMP compliance; technical documentation; scientific writing; literature research; analytical thinking and problem‑solving.

Behavioral and Execution

Ownership and accountability; independent decision‑making; collaboration within multidisciplinary teams; effective written and verbal communication; continuous learning; innovation and new‑product idea generation.

DESIRED CANDIDATE PROFILE

The ideal candidate will be a technically sound, self‑driven pharmaceutical professional with strong hands‑on formulation development experience, regulatory awareness, and the confidence to independently evaluate product quality and formulation suitability. The candidate should demonstrate ownership, sound scientific judgment, effective communication, and the ability to work collaboratively with cross‑functional teams.

OTHER CONSIDERATIONS

This job description is intended to provide a general overview of the role’s responsibilities and expectations. It is not an exhaustive list of all duties. Responsibilities may change in response to evolving business priorities, portfolio requirements, and organizational needs.