Sai Life Sciences is Hiring for R&D Pharma Jobs | Bengaluru Drive for Hyderabad Positions

Join Sai Life Sciences‘ walk-in interview in Bengaluru for cutting-edge R&D pharma jobs. Ideal for MSc Organic Chemistry experts with 2-8 years experience. Boost your pharmaceutical careers in India at a global CRDMO leader.

About the Company

Sai Life Sciences, founded over 25 years ago, is a premier full-service Contract Research, Development, and Manufacturing Organization (CRDMO) specializing in small molecule NCE programs for global pharma and biotech clients.

With end-to-end services from discovery to commercial API manufacturing, it excels in innovation through advanced R&D centers and CMC expertise, serving over 280 international partners.

Certified as a Great Place to Work (April 2025–April 2026) and compliant with USFDA, EMA, and PMDA standards, Sai drives sustainable growth with facilities in India, the UK, and USA, employing 3,400+ professionals. Recent expansions, including a new CMC center doubling capacity by 2026, underscore its rapid rise as India’s fastest-growing CRDMO.

For more R&D jobs and pharma opportunities, visit Pharma Recruiter.

Job Details

• Company Name: Sai Life Sciences
• Experience: 2-8 Years (up to 14 years for select roles)
• Qualification: MSc (Organic Chemistry/Life Sciences: Microbiology, Biochemistry, Biotechnology); B.Tech/BE/ME (Chemical Engineering); M.Pharm (Pharmacology); M.Pharm/PhD
• Location: Hyderabad, Telangana
• Work Type: On-site

Job Description

Sai Life Sciences is recruiting top talent for its Hyderabad-based R&D and engineering teams to fuel innovation in drug discovery and development. This Bengaluru walk-in drive targets experienced professionals in analytical, process, and biological sciences to support global CRDMO projects. Contribute to high-impact NCE programs in a collaborative, state-of-the-art environment.

Analytical R&D

• Department: Analytical R&D
• Market: Small Molecule Drug Development
• Role: Develop and validate analytical methods for APIs and intermediates
• Experience: 2-8 Years
• Education/Qualification: MSc

Process R&D

• Department: Process R&D
• Market: Small Molecule Drug Development
• Role: Design scalable synthetic routes for pharmaceutical compounds
• Experience: 2-8 Years
• Education/Qualification: MSc (Organic Chemistry)

Particle Sciences & Engineering

• Department: Particle Sciences & Engineering
• Market: Small Molecule Drug Development
• Role: Optimize particle engineering for formulation and process efficiency
• Experience: 2-8 Years
• Education/Qualification: B.Tech (Chemical Engineering)

Process Engineering

• Department: Process Engineering
• Market: Small Molecule Drug Development
• Role: Scale-up and troubleshoot manufacturing processes for APIs
• Experience: 2-8 Years
• Education/Qualification: BE/ME (Chemical Engineering)

Biology – In Vitro

• Department: Biology
• Market: Small Molecule Drug Development
• Role: Conduct in vitro assays for drug screening and mechanism studies
• Experience: 2-8 Years
• Education/Qualification: MSc (Life Sciences: Microbiology, Biochemistry, Biotechnology)

Biology – In Vivo

• Department: Biology
• Market: Small Molecule Drug Development
• Role: Lead in vivo pharmacology studies for efficacy and safety evaluation
• Experience: 2-8 Years
• Education/Qualification: M.Pharm (Pharmacology)

DMPK

• Department: DMPK
• Market: Small Molecule Drug Development
• Role: Perform ADME studies to optimize drug pharmacokinetics
• Experience: 2-14 Years
• Education/Qualification: M.Pharm/PhD

Skills/Qualifications

• Advanced degree in chemistry, engineering, or life sciences with R&D experience
• Expertise in analytical method validation, organic synthesis, or biological assays
• Proficiency in regulatory compliance (USFDA, EMA) and QMS for global markets
• Strong problem-solving and collaboration skills in multidisciplinary teams
• Knowledge of scale-up processes, particle engineering, or DMPK modeling

Key Responsibilities

• Validate analytical methods for impurity profiling
• Scout and optimize synthetic routes for efficiency
• Engineer particles for enhanced bioavailability
• Scale processes from lab to commercial production
• Execute in vitro/in vivo studies for lead optimization

Benefits/Perks

• Career advancement in a top CRDMO with 25+ years legacy
• Cutting-edge training in discovery and CMC innovations
• Competitive salary and global project exposure
• Inclusive culture certified as Great Place to Work
• Sustainability initiatives and work-life balance support

How to Apply

Register by scanning the QR code in the original posting or visit sailife.com to apply via the careers portal. Walk in with your resume, certificates, and ID for direct interviews. Sai Life Sciences charges no fees—apply securely.

Verified Post

The post is released by the Sai Life Science LinkedIn page. Click here to visit the post

For more QA jobs, QC jobs, or production jobs, explore Pharma Recruiter. Elevate your R&D pharma jobs journey—register today!

Walk-in Interview Details

• Date: November 15 & 16, 2025
• Time: 9:00 AM to 5:00 PM
• Venue: Sai Vishram Business Hotel, Hebbagodi, 144-C/1, Kirloskar Road, opp. MTR, Bommasandra Industrial Area, Bengaluru, Karnataka 560099

Why You Should Join

Sai Life Sciences cultivates a family-like, innovative culture certified as a Great Place to Work, where professionals thrive amid rapid growth and global collaborations. With long-term stability in a fastest-growing CRDMO, you’ll access endless learning in cutting-edge R&D and CMC, from peptide advancements to facility expansions.

Embrace a compliant, sustainable environment fostering work-life balance and impactful contributions to 280+ clients’ drug pipelines, securing your trajectory in pharmaceutical careers in India.

FAQs