New Product Development Manager

Femacare; Dadri; On-site; INR 609,000 - 730,000; Full time

Job summary

Cosma Fertility is expanding its team in Noida for a role focused on New Product Development and Clinical Partnerships. You will manage the pipeline after FertiGen, coordinate trials, and oversee regulatory dossiers and safety reporting.

The position requires field-facing experience with OB-GYNs or women's health, and the ability to communicate complex mechanisms to both patients in Hindi and doctors in technical terms. On-site role with travel.

Qualifications

• Experience coordinating clinical partnerships and trials.
• Ability to explain mechanisms to doctors and patients clearly.
• Track record in regulatory dossiers and safety reporting.

Responsibilities

• Own the product development pipeline post-FertiGen.
• Coordinate clinical trials: enrolment pace, site issues, ethics files, CRFs.
• Manage regulatory documentation and scientific communications with doctors.
• Maintain safety reporting with timely adverse event escalation.
• Define the claims boundary for product messaging.

Skills

Clinical liaison

Regulatory documentation

Doctor communication

Field-facing experience

Education

Biomedical engineering / Biotechnology / B.Pharm / M.Pharm / Life sciences

Job description

New Product Development & Clinical Partnerships

Were hiring

the person who will help build what comes after FertiGen while managing our clinical relationships.

Cosma Fertility makes FertiGen, a CDSCO-approved, non-hormonal fertility support device developed at IIT Bombay. Were a Forbes India-listed company, National Startup Award winner, and Prix Galien India Top 3 nominee

What you will own

• The product pipeline — what comes next after FertiGen. Literature, feasibility, specification, and the work with our academic and manufacturing partners.
• Product and technical documentation, and support on regulatory dossiers.
• Clinical trial coordination — enrolment pace, site problems, ethics committee files, case report forms.
• Doctor-facing scientific communication and KOL relationships.
• Safety reporting. Adverse events logged and escalated correctly, on time, every time.
• The claims boundary. You hold the line on what we can and cannot say about our products.

You will fit if

• You have a biomedical engineering, biotechnology, B.Pharm, M.Pharm or life sciences background.
• You have 4–8 years, with real field-facing time — clinical specialist, medical affairs, senior MR or CRA.
• You have worked with OB-GYNs, in women’s health, or in medical devices and diagnostics.
• You have been part of a product going from idea to specification, or a trial from protocol to site.
• You can explain a mechanism in plain Hindi to a patient and in technical terms to a doctor, in the same hour.
• You follow up without being reminded.

Please do not apply if

• Your background is purely lab-based and you have never spoken to a practising doctor.
• You need a written instruction before every task.
• You treat regulatory paperwork as somebody else’s job.

Details

60,000 per month. Noida, on-site, with travel to trial sites, clinics and manufacturing partners