A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post: Senior Pharmaceutical Scientist
Job Description:
•Delivers formulation and process to expected quality in the timeframe and budget required by the target product profile.
Functional Description
•Performs or manages the innovation, development and validation of formulas and manufacturing process within high quality standards for new OTC products for Novartis Consumer Health, both North American and Global business units.
•Participates in Project Teams, assessing the viability of proposed projects, trouble¬shooting, finding solutions and championing new product ideas.
•Manages projects against timelines and budgets while maintaining high quality standards.
•Supervises or conducts the manufacture and packaging of R&D at batches, i.e. prototypes, experimental formulas, stability, clinical supply and validation batches.
•Provides clinical supplies for clinical studies, market research studies and sales samples.
•Has close interaction with Manufacturing Operations, Engineering, Quality, Marketing, Sales, Market Research, Creative Services and all other departments in OTC R&D.
•Works on global projects; supports maintainance of GMP compliant facilities.
Candidate Profile:
•Degree in pharmaceutical sciences (including Pharmacology, Pharmaceutical/Pharmacy, Medicinal Chemistry, Pharmacognosy) or related disciplines, or equivalent experience.
•Experience in pharmaceutical manufacturing development of multiple dosage forms at pilot and commercial scale under GMP conditions.
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Candidate Profile:
•Self motivated and directed, showing creativity and initiative.Key Distinguishing Responsibilities
•Plans and conducts experiments of a high degree of complexity.
•Makes scientific presentations to internal management and external customers.
•Coordinates or manages capital purchases and validation activities as required.
•Consolidates and analyzes data from various sources, draws conclusions and recommends scientific solutions as required.
•Works with R&D contractors.
•Participates on manufacturing site project teams.
•Writes CMC section of INDs, ANDAs, NDAs, CTAs and CTDs for submission to Health Authorities.
•Assists in creation of development timelines and other project management activities.
• Perform other duties as deemed appropriate.
Skill Requirements and Competencies (Shared Values)
• Excellent analytical skills, displays conceptual thinking.
• Excellent written and oral communication skills.
• Experience in managing pharmaceutical development projects.
• The support and promotion of the Novartis Compliance Program (Novartis Standards of Ethics & Conduct) is an essential element of the performance standards and will be used in the overall performance standards and the overall performance ratings.
Experience
• M Pharm with at least 7 years of relevant experience.
• PhD with at least 5 years of experience.
Additional Information:
Location: Hyderabad
Education: M.Pharm, Ph.D
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
Division: Over The Counter
Job Type: Full Time
Employment Type: Permanent
Job ID: 88239BR
End Date: 11th April, 2012
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