Intern, Product Development

Sun Pharmaceutical Industries Ltd•Brampton, ON

2d•Onsite

About The Position

Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients. As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being.

Requirements

Undergrad 3rd or 4th year – Pharmacy/ Chemistry/ Biology/ Chemical Engineering/ Biochemistry prefer University. GPA 3.0
Basic knowledge of liquid and semi-solid formulation development
Laboratory experience is required
A general understanding of GMP
Familiarity with Microsoft word processing and Excel spreadsheet programs is required
Ability to work effectively in a team-based environment
Good organizational skills and multi-tasking skills to facilitate the timely completion of projects
Good written and verbal communication skills
Utilize and apply basic scientific knowledge and semi-solid theories to design effective experiments
Evaluate and assess formulations and processes based on analytical results
Collaborate with manager team and other R&D professionals, plant staffs, administration staffs effectively to solve any issues or conflicts during product development

Responsibilities

Assist in the development of formulae and process for new products -- this includes literature searching, preparing lab scale developmental batches, executing experiments to support the final formulation and process.
Write Master Formula and Packaging Work Orders for Exhibit Batches and Facilitate manufacturing and the packaging of exhibit batches.
Report and clearly document all research work performed -- this includes documentation of protocol, experimental process, problems, and observations.
Participate in activities leading to Technical Transfer, process validation, and commercial production troubleshooting under the guidance of Senior Associate/Manager.
Assist in planning project development activities proactively, update outcomes, and completion of the activities in a timely manner.
Maintain a clean laboratory environment and ensure that safety regulations are followed.
Other activities to comply with GMP/GLP requirement.
Complete GMP training for updated SOPs, and complete all GMP activities and documentation correctly and in a timely manner.
Other duties as assigned.
Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day