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Regulatory Affairs Executive

Pune, MH, India

Regulatory Affairs Executive — Job Description

DesignationRegulatory Affairs Executive
Department / DivisionRegulatory Affairs
Reports toManaging Director
LocationPune HQ (Shivajinagar) – Kamala Classic, Ghole Road
Employment typeFull-time, Permanent
Experience3–6 years in regulatory affairs for devices / IVD
EducationM.Pharm / M.Sc (Life Sciences); RA certification preferred
TravelOccasional (authorities/OEM)
Openings0
Key interfacesMD, Purchase, Tender team, OEM regulatory teams, Authorities

Role purpose

Keep every product Dawell imports and sells legally registered, licensed and tender-ready.

Manage regulatory affairs and product compliance for imported detection/medical devices (CDSCO, BIS, legal metrology and import licensing).

Key responsibilities

  • Handle device registration, import licences and CDSCO/BIS compliance
  • Maintain regulatory dossiers, certificates and renewals
  • Support tenders with compliance and statutory documents
  • Liaise with authorities and OEMs on regulatory matters
  • Track regulatory changes impacting the portfolio
  • Track the medical-device and IVD rules (MDR 2017) for licensed products
  • Maintain the regulatory document library used in tenders

System responsibilities (Odoo)

  • Device registration, import licences and CDSCO/BIS/legal-metrology compliance
  • Maintains regulatory dossiers, certificates and renewals; supplies tender statutory docs

Key result areas & indicative targets

KRA / KPIIndicative target
Licence/registration currency & renewalsZero lapsed licences
Dossier completeness100% of active products with dossiers
Tender compliance-doc TATDocuments within 1 working day of request
Zero regulatory non-complianceZero notices

Targets are indicative and are finalised in the KRA appraisal for each financial year.

Qualifications & experience

  • M.Pharm / M.Sc (Life Sciences); RA certification preferred
  • Experience: 3–6 years in regulatory affairs for devices / IVD

Technical skills

  • Regulatory affairs
  • CDSCO/BIS
  • Documentation
  • Liaison
  • CDSCO / MDR 2017 & IVD rules
  • BIS / legal metrology
  • Import licensing
  • Regulatory dossiers

Skill catalogue (Odoo): Service reports & documentation, Technical compliance & bid evaluation

Behavioural competencies

  • Accountability & reliability
  • Clear communication
  • Learning agility & technical curiosity
  • Attention to detail
  • Customer & service orientation
  • Precision
  • Persistence
  • Liaison skills

Certifications & compliance

  • Regulatory affairs certification (preferred)
  • Adherence to Dawell HR Policies v2.0 (POL/00–23), incl. POL/02 Attendance, POL/05 Travel & Expenses, POL/22 Delegation of Authority

Working conditions

Pune HQ; visits to authorities

Career path

RA Executive → RA Manager

Selection process

  1. Application & CV screening (HR, within 5 working days)
  2. HR screening call
  3. Technical / product round
  4. Manager interview (Head / MD for senior roles)
  5. Offer & reference check
  6. Joining & induction (Dawell eLearning + POL/00–23 policy acknowledgement)

About Dawell Lifescience

Dawell Lifescience Pvt. Ltd. (Pune) is an authorised Indian partner for forensic, narcotics, toxicology, counterfeit-detection and public-safety technologies — Thermo Fisher (TruNarc, TruScan, Gemini), Abbott SoToxa, Dräger (alcohol, drug testing, CBRN, SCBA, gas detection) and FARO 3D crime-scene systems — serving police, forensic labs, excise, health / FDA, defence, CAPF and PSU buyers through tenders, GeM and direct orders.

Customer Relationship
Personal Evolution
Autonomy
Administrative Work
Technical Expertise

Regulatory Affairs Executive

Keep every product Dawell imports and sells legally registered, licensed and tender-ready.

Location: Pune HQ (Shivajinagar) – Kamala Classic, Ghole Road  ·  Type: Full-time, Permanent  ·  Experience: 3–6 years in regulatory affairs for devices / IVD

What you will do

  • Handle device registration, import licences and CDSCO/BIS compliance
  • Maintain regulatory dossiers, certificates and renewals
  • Support tenders with compliance and statutory documents
  • Liaise with authorities and OEMs on regulatory matters
  • Track regulatory changes impacting the portfolio
  • Track the medical-device and IVD rules (MDR 2017) for licensed products
  • Maintain the regulatory document library used in tenders

What you bring

  • M.Pharm / M.Sc (Life Sciences); RA certification preferred
  • Experience: 3–6 years in regulatory affairs for devices / IVD
  • Regulatory affairs
  • CDSCO/BIS
  • Documentation
  • Liaison
  • CDSCO / MDR 2017 & IVD rules
  • BIS / legal metrology
  • Precision
  • Persistence
  • Liaison skills

Good to have

  • Regulatory affairs certification (preferred)

What we offer

  • Work with world-leading forensic, narcotics and public-safety technology
  • OEM product training and certifications
  • Direct impact on public safety and the Drug-Free India mission
  • Statutory benefits (PF, ESIC where applicable, gratuity), leave as per POL/01, travel and daily allowance as per POL/05
  • Structured appraisal (KRA based) and career path

About Dawell Lifescience

Dawell Lifescience Pvt. Ltd. (Pune) is an authorised Indian partner for forensic, narcotics, toxicology, counterfeit-detection and public-safety technologies — Thermo Fisher (TruNarc, TruScan, Gemini), Abbott SoToxa, Dräger (alcohol, drug testing, CBRN, SCBA, gas detection) and FARO 3D crime-scene systems — serving police, forensic labs, excise, health / FDA, defence, CAPF and PSU buyers through tenders, GeM and direct orders.

How we hire

  1. Application & CV screening (HR, within 5 working days)
  2. HR screening call
  3. Technical / product round
  4. Manager interview (Head / MD for senior roles)
  5. Offer & reference check
  6. Joining & induction (Dawell eLearning + POL/00–23 policy acknowledgement)

Dawell Lifescience is an equal-opportunity employer. Your data is processed only for recruitment, as per our privacy notice (DPDP Act 2023).