Hiring for multiple roles in DMPK ( In Vitro ADME, Metabolism / physicochemical / Transporters / Bioanalysis)

Department:

Location:

About Sai:

Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels.

Roles in DMPK we are hiring for :

• Bioanalytical / Peptides, Antibody drug conjugates and ASOs
• In vitro ADME / cell biology, cell permeability hepatocytes, 3D cultures, image analysis, drug transporters and enzymology
• PK/PD, Modeling and Simulations / Pheonix WinNonlin, R, Monolix, NONMEM, MATLAB, or any other custom-built software
• In vitro Toxicology/ 3D cultures-Organoids and Spheroids

Key Responsibilities

• To work on Drug Discovery project providing DMPK support.
• Knowledge of data compilation and interpretation for test compound classification systems, either as substrates or uptake inhibitors.
• Ability to understand and read data, identify data variability, and participate in data review cycles with the QA team.
• Commitment to delivering data within agreed timelines (< 7 days) and strong work ethics to complete assigned tasks.
• Excellent communication and collaboration skills, working closely with team members.
• Good oral and written communication skills.

Education and Experience:

• M Pharm (Pharmacology/Pharmaceutics) with 3-8 years of experience or MSc with 6-8+ years of experience in DMPK of small molecule drug discovery and development, preferably in a CRO or Biotech/Pharma industry.
• Knowledge of FDA and EMA industry guidance.