Strides Pharma Hiring for Project Management, Analytical Services & Regulatory Affairs

Strides Pharma Careers 2025 Job Opportunities in Bangalore

Strides Pharma Science Limited is seeking talented professionals for multiple roles in Project Management, Analytical Services (R&D), and Regulatory Affairs at their Bangalore location. If you have relevant industry experience and are looking for career growth in the pharmaceutical industry, this is an excellent opportunity!

Project Management – R&D (Bangalore)

Key Responsibilities:

• Drive project planning and execution from new product initiation to dossier filing and approval across multiple geographies.
• Implement governance mechanisms to monitor and manage diverse projects.
• Assist in executing strategic projects, including in-house and outsourced initiatives.
• Lead cross-functional collaboration with internal and external stakeholders.
• Assist in cost estimation and budget planning for projects.

Eligibility Criteria:

• Qualification: Bachelor’s or Master’s in Pharmacy, Chemistry, or Life Sciences.
• Experience: 4-7 years in Project Management for R&D.
• Skills: Strong understanding of pharma regulations, budget planning, and cross-functional coordination.

Send your resume to Navya@arcolab.com to apply!

Analytical Services – R&D (Bangalore)

Key Responsibilities:

• Operate analytical instruments such as HPLC, GC, Dissolution, PSD, ICP-MS, XRD.
• Ensure proper documentation as per GLP (Good Laboratory Practices).
• Conduct calibration of analytical instruments.
• Perform method validation and method transfers in R&D.

Eligibility Criteria:

• Qualification: B.Pharm/M.Pharm/M.Sc. in Analytical Chemistry, Pharmaceutical Sciences, or related field.
• Experience: 1-4 years in Analytical R&D, Quality Control, or Method Development.
• Skills: Expertise in instrument calibration, method validation, and regulatory compliance.

Apply now by sending your resume to Navya@arcolab.com.

Regulatory Affairs – Emerging Markets (Bangalore)

Key Responsibilities:

• Develop and execute regulatory strategies for SEA, GCC, CIS, Latam, and African markets.
• Lead regulatory dossier preparation, submission, and approvals.
• Ensure compliance with post-market surveillance and reporting obligations.
• Collaborate with cross-functional teams to meet global regulatory requirements.

Eligibility Criteria:

• Qualification: B.Pharm/M.Pharm/M.Sc. in Regulatory Affairs, Pharmaceutical Sciences, or Life Sciences.
• Experience: 10-15 years in Regulatory Affairs for Emerging Markets.
• Skills: Strong knowledge of global regulatory pathways, dossier submission, and market compliance.

Interested? Share your profile at Navya@arcolab.com.

Quick Job Summary

📩 Apply Now – Send your resume to Navya@arcolab.com for further discussions!