Wednesday, May 27, 2026

CogScientia Pvt Ltd hiring for Medical Writer || WFH || Remote || Apply here

🚨 Hiring Alert | Medical Writer | Remote (India)
We are looking for an experienced Medical Writer to join our growing team at CogScientia Pvt Ltd.
📍 Location: Remote – India
🕒 Job Type: Full-time
📌 Experience: Minimum 3 Years

🔬 Key Responsibilities:
  • Develop scientific and medical content for slide decks, newsletters, video storyboards, social media posts, leaflets, etc.
  • Create engaging educational materials for healthcare professionals and patients.
  • Review and edit content for accuracy, clarity, and consistency.
  • Manage multiple projects while meeting deadlines
✅ Requirements:
  • Bachelor’s degree in Life Sciences / Medical / Pharmacology / Biotech / Nutrition.
  • Strong medical writing experience.
  • Excellent writing, editing & proofreading skills.
  • Good understanding of medical terminology and scientific data interpretation.
  • Proficiency in MS Office
✨ What We Offer:
  • Competitive salary.
  • Career growth opportunities.
  • Supportive and collaborative work culture
If you or someone in your network is interested, please share your updated resume.

Walk In interview at Global Calcium for Quality Assurance position on 05/06/2026

 

Resonacle Life Sciences hiring for Analytical Development Head – R&D || Apply now

🚨 Hiring | Analytical Development Head – R&D 🚨

We are hiring for an Analytical Development Head – R&D role with a leading MNC pharmaceutical company.
🔹 15+ years of experience in Pharma Analytical R&D
🔹 Expertise in method development, validation, stability studies & regulatory compliance
🔹 Strong leadership and team handling experience preferred

Location - PAN India

📩 Interested candidates can share their updated CV with subject Line "Analytical Development Head" at prabha.parad@resonacle.com

ArcherChem Hiring for Regulatory Affairs Manager || Apply now

🚨 We’re Hiring | Regulatory Affairs Manager – US Market

📍 Location: Malad, Mumbai
🏭 Industry: Pharmaceutical Formulations
💼 Experience: 7–15 Years

Key Responsibilities:
  • Lead and manage regulatory submissions, renewals, amendments, and approvals for the US market.
  • Prepare, review, and compile CTD / eCTD dossiers as per regulatory requirements.
  • Coordinate with R&D, QA, QC, Manufacturing, and other cross-functional teams for documentation and submissions.
  • Handle regulatory deficiency responses, queries, variations, supplements, and post-approval lifecycle activities.
  • Ensure compliance with USFDA guidelines and applicable international regulatory requirements.
  • Review technical documents including stability data, specifications, validation reports, and product-related dossiers.
  • Support new product launches and ensure timely regulatory approvals.
  • Maintain regulatory records and monitor timelines for submissions and renewals.
  • Assist during regulatory audits and inspections

Desired Candidate Profile:
✅ Graduate / Post-Graduate in Pharmacy / Life Sciences
✅7–15 years of experience in Regulatory Affairs within pharmaceutical formulations
✅Strong knowledge of USFDA regulations, CTD/eCTD submissions, and dossier compilation
✅Experience in ANDA/NDA documentation and lifecycle management preferred


📩 Interested candidates may share their updated resume at:

Friday, May 22, 2026

VerGo Pharma Research Laboratories Pvt. Ltd., is hiring the Prduction & QC positions


VerGo Pharma Research Laboratories Pvt. Ltd., Verna is hiring the following positions

Department: Production
Position: Executive
Qualification: B. Pharm/ M. Pharm
Experience: 5-6 years in the Granulation, compression and coating.


Department: Quality Control
Position: Executive
Qualification: B. Sc./ M. Sc.
Experience: 2-4 years in validation, should have thorough knowledge of HPLC.


Interested candidates can forward their resumes to hra1@vergolabs.com