Senores Pharmaceuticals Walk-in Interview – ADL, Regulatory Affairs & Pharmacovigilance Roles on 29th March 2026

Pharma R&D & Regulatory Jobs – Senores Pharmaceuticals, a thought-leading company committed to global wellness and high-quality formulations, is conducting a walk-in interview on 29th March 2026 for Technology Transfer (US Market), ADL (US Market), Regulatory Affairs (US/EU/ROW), and Pharmacovigilance/Regulatory Documentation positions at its R&D Centre in Ahmedabad.

This is a strong opportunity for experienced professionals with expertise in scale-up, method validation, stability studies, ANDA evaluation, dossier preparation, and PV processes to join a fast-expanding organization focused on regulated markets.

About the Company

Senores Pharmaceuticals is an emerging pharmaceutical company dedicated to innovation and manufacturing of highest international quality standards to meet global healthcare demands.

With a strong focus on regulated markets (US, EU, ROW), the company is rapidly expanding its R&D capabilities in technology transfer, analytical development, regulatory affairs, and pharmacovigilance.

Senores operates with a commitment to quality, compliance, and continuous improvement, offering a dynamic environment for professionals to contribute to global product development and lifecycle management.

Job Details

• Company Name: Senores Pharmaceuticals
• Experience: Varies by role (2–8 Years)
• Qualification: B.Pharm / M.Pharm / M.Sc
• Location: Ahmedabad (R&D Centre)
• Work Type: On-site

Job Description

Senores Pharmaceuticals is strengthening its R&D and regulatory teams to support expansion in regulated markets. The walk-in targets experienced candidates for roles in technology transfer, analytical development, regulatory affairs, and pharmacovigilance with a focus on US/EU/ROW submissions and compliance.

Technology Transfer (US Market) – Officer / Executive / Sr. Executive

• Department: Technology Transfer
• Market: Pharmaceuticals – Regulated Markets (US)
• Role: Officer / Executive / Sr. Executive – Technology Transfer
• Experience: Officer: 2–3 Years | Executive: 3–5 Years | Sr. Executive: 5–8 Years
• Education/Qualification: B.Pharm / M.Pharm

ADL (US Market) – Officer / Executive / Sr. Executive

• Department: Analytical Development Laboratory (ADL)
• Market: Pharmaceuticals – Regulated Markets (US)
• Role: Officer / Executive / Sr. Executive – ADL
• Experience: Officer: 2–3 Years | Executive: 3–5 Years | Sr. Executive: 5–8 Years
• Education/Qualification: M.Pharm / M.Sc

Executive Documentation (ADL & Technology Transfer)

• Department: Documentation
• Market: Pharmaceuticals – Regulated Markets
• Role: Executive – Documentation
• Experience: 3–5 Years
• Education/Qualification: B.Pharm / M.Pharm

Regulatory Affairs (US/EU/ROW Market) – Executive / Sr. Executive

• Department: Regulatory Affairs
• Market: Pharmaceuticals – Regulated Markets (US/EU/ROW)
• Role: Executive / Sr. Executive – Regulatory Affairs
• Experience: 5–8 Years
• Education/Qualification: M.Pharm

Executive – Pharmacovigilance / Regulatory Documentation & Due Diligence

• Department: Pharmacovigilance / Regulatory
• Market: Pharmaceuticals – Regulated Markets
• Role: Executive – Pharmacovigilance / Regulatory Documentation
• Experience: 2–7 Years
• Education/Qualification: M.Pharm

Skills/Qualifications

• Strong experience in scale-up, exhibit batches, tech transfer (IR/SR/ER), troubleshooting, and ANDA evaluation
• Proficiency in HPLC, GC, dissolution, method development/validation, stability studies, and analytical documentation
• Expertise in dossier preparation, global submissions, post-approval lifecycle management, and regulatory compliance
• Knowledge of PV processes, due diligence, CFT coordination, and ICH guidelines
• Excellent documentation, communication, and problem-solving skills
• Experience in US/EU/ROW regulatory submissions is highly preferred

Key Responsibilities

• Execute technology transfer from R&D to commercial scale for US market
• Perform analytical method development, validation, and stability studies
• Prepare and review BMR, specifications, STPs, and regulatory documentation
• Support post-approval changes, lifecycle management, and due diligence
• Handle PV activities, dossier documentation, and regulatory submissions
• Ensure compliance with cGMP, ICH guidelines, and global regulatory standards

Benefits/Perks

• Career growth in a fast-expanding regulated pharma company
• Exposure to US/EU/ROW regulatory submissions and advanced analytical techniques
• Opportunities for skill enhancement in tech transfer, validation, and PV
• Competitive compensation aligned with experience
• Supportive work culture focused on quality and innovation

How to Apply

Walk-in interview is open on 29th March 2026 (Sunday) from 10:00 AM to 3:00 PM. Bring updated resume, educational certificates, experience letters, and relevant documents.

Candidates unable to attend can email CV to career@senorespharma.com or contact +91 99980 14064. For more regulatory affairs jobs, ADL openings, tech transfer roles, and pharma walk-in interviews in Ahmedabad/Gujarat, visit Pharma Recruiter.

Walk in on 29th March 2026 and be part of Senores Pharmaceuticals’ strategic expansion in regulated markets!

Walk-in Interview Details

• Date: 29th March 2026 (Sunday)
• Time: 10:00 AM – 3:00 PM
• Venue: R&D Centre: Arrow House, Opp. Symphony House, Opp. Hotel Grand Bhagwati, S G Highway, Ahmedabad
• Contact/Email: career@senorespharma.com | +91 99980 14064

Why You Should Join

Senores Pharmaceuticals offers a dynamic, growth-oriented environment ideal for professionals passionate about regulated markets and complex formulations.

With a strong focus on US/EU/ROW submissions, tech transfer, analytical development, and pharmacovigilance, the company provides meaningful work, skill enhancement, career progression, and the opportunity to contribute to global healthcare.

Joining Senores means being part of a forward-looking organization committed to innovation, quality, and excellence in the pharmaceutical industry.

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