Job Description

Job Description

Job Description

Solaris Pharma Corporation is a leading specialty pharmaceutical company committed to the identifying, developing and marketing of high-quality, complex, generic and specialty pharmaceutical products. With a thorough knowledge of the development life cycle and well-trained, committed scientific personnel, Solaris Pharma Corporation has streamlined processes that are efficient in reducing development costs and shortening timelines, without compromise in quality.
Solaris Pharma Corporation is dedicated to developing a broad portfolio of generic and specialty pharmaceutical products and providing early access to complex generic products for patients. Solaris Pharma Corporation benefits from its technical expertise, R&D, regulatory and commercialization strength in the development of specialized generic & branded pharmaceutical products. Our pipeline which encompasses products from multiple dosage forms include but not limited to sterile, dermatological, tablet products among others which are challenging to develop and manufacture with complexities arising from formulation & process development, regulatory hurdles, stability and scale up.
Solaris Pharma Corporation is currently engaged in the development of several generic products and is committed to establish itself as a pacesetter in pharmaceuticals. Solaris Pharma Corporation, is looking for a full time, Jr. Research Scientist.
Responsibilities:
Independently creating and implementing formulation development strategies. Design, direct and/or conduct pre-formulation, formulation development, process development, process optimization, scale-up and clinical manufacturing on assigned projects of Generic Formulations.

• Prepare and execute the lab scale developmental batches for Topical products (Creams, Ointments, Gels etc...)
• Formulation and interpretation of results.
• Writing lab note book and compilation of results for each project in up-to- date fashion.
• Conduct a pre-formulation studies and stability of development batches as and when required during development.
• Review and authorize reports/documents such as master formulas and other key reports/ documents.
• Help assist scientists for Development of Rheological characteristic for Semi-Solid Products
• Assist in the manufacture of ANDA submission batches and execution of protocols for Topical Products
• Coordinate with contract research organizations for scale up & clinical batches and provide technical assessments
• Help assist Scientist in daily routine formulation activity

Qualifications:

• Master with 0-1 years in Pharmaceutics or related field in semi-solid (preferred) or related product development
• Must have excellent communication skills, organizational ability and good documentation capabilities
• Working experience in the development of semi-solid generic products.
• Experience with dosage forms such as suspensions and emulsions is a plus
• Excellent technical writing skills (Feasibility reports on new opportunities, technical due diligence supportive documents, experimental protocols, development reports, and technology transfer reports)
• Experience in both brand and generic industry is a plus

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