Our Company:
Global Value Web(GVW) drives business transformation for Pharma & Life Sciences, Healthcare and Energy organizations by connecting the dots across their value chain and enabling operational excellence in their digital transformation journey.
Our solutions & services integrate People, Data, Process, and Technology that
enable our clients to optimize operational efficiencies, maximize financially
results, and allow them to serve their customers better.
Our People:
Our people have a rich tradition of working side by side with our customers as long-term partners, developing tailored solutions that help customers deliver business success in their local markets. Every day, with our passion, commitment to excellence, and innovation, our people create specialized and custom solutions designed to make our customer’s businesses sustainable and run seamlessly.
Key Responsibilities:
Responsible for providing analytical support for the developmental projects/comparative dissolution projects received from other Janssen sites.
Responsible to be an interface with contract laboratories, suppliers, customers, and peers to define and improve project performance and expectations.
Responsible for coordinating with CRO and ensuring that the project is complete within
Designs scientific experiments. Actively and personally monitor lab work. Recommends expansion or curtailment of investigations on the basis of experimental results or scientific.
Responsible for the preparation of test methods, technical documents, protocols, and reports whenever required
Is responsible for the proper recording of ensures that records and raw data are properly retained. Summarizes, interprets, reviews data, and draws conclusions.
Analyzing and drawing interpretation out of the dissolution data
Troubleshooting the problems associated with instruments or
Performing activities following the GMP/ safety requirements related to the assigned
Key Interaction:
Drug Product Development, JSC stakeholders, Regulatory CMC/LOC, Spec management team
Quality & Compliance Responsibilities:
Is responsible for the proper recording of ensures that records and raw data are properly retained.
Position Requirements:
Education & Certifications MSc. or M.Pharm
Experience – More than 7/8 Years of industrial experience in formulation or Analytical development, dissolution development experience preferred.
Functional Competencies (Skills, Knowledge, and Attributes): –
Multimedia Dissolution testing
Knowledge of Regulatory Guidelines on dissolution studies g. FDA-SUPAC and ICH for validations and other emerging markets. like China, Latin America
Behavioral Competencies (Leadership Imperatives):
Good communication and presentation skills
Should a team player
Decision-making capabilities
Good Collaborative skills
Planning and execution
Key Selection Criteria
Knowledge of In vitro dissolution testing
Comparative dissolution testing, including multimedia dissolution
Interface with contract labs
Dissolution
Basic knowledge of the formulation (Oral solid dosage forms)
What’s On Offer?
A challenging and growing position with the opportunity to work in one of the emerging global organizations with services in the healthcare and life sciences industry, and the chance to professionalize the organization via innovation. This is in combination with a full-time position.
Your Application:
If your background and personal experience fit this profile, please send us your complete application with your latest resume.
Job Title : Manager AD – Dissolution Science
Experience : 7-8 years
Position Type : Full time
Base Location : Mulund, Mumbai
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