Careers at Aprazer

Opportunities to Grow

Click on a role to view details. We are building a positive, productive work environment.

HR Assistant/Executive

Location: New Delhi (On-site) | Experience: 2-3 Years
▾
Role Description

This is a full-time, on-site role for an HR Assistant/Executive at Aprazer Healthcare, located in New Delhi. The role involves providing support to the Human Resources department in daily administrative tasks, recruitment coordination, employee engagement activities, and compliance documentation. Collaboration with multiple teams is key.

Key Responsibilities
  • Recruitment: Assist in posting ads, screening resumes, and scheduling interviews.
  • Employee Records: Maintain and update digital and physical employee files.
  • Onboarding/Offboarding: Prepare offer letters, contracts, and onboarding kits; support exit formalities.
  • Operations: Handle attendance, leave records, and payroll inputs; assist in drafting policies.
  • Engagement: Organize training, workshops, team-building, and support grievance handling.
Qualifications & Skills
  • Bachelor’s degree in HR Management or Business Administration.
  • 2-3 years of experience (Pharma/Healthcare exposure preferred).
  • Basic knowledge of HRMS and payroll systems.
  • Proficiency in MS Office (Excel, Word, PowerPoint).
  • Strong multitasking and communication skills.
Apply for this Role

Sales Executive (Female)

Location: Delhi NCR | Experience: 2-5 Years
▾
Role Description

We are seeking a motivated and dynamic Female Sales Executive to drive sales of branded generic pharmaceutical products across the Delhi NCR region. This involves building strong relationships with doctors, pharmacies, and distributors while ensuring industry compliance.

Key Responsibilities
  • Promote and sell branded generic medicines to healthcare professionals.
  • Maintain customer relationships to achieve sales targets.
  • Conduct market visits to identify new business opportunities.
  • Ensure timely payment collection and documentation.
  • Organize product presentations and promotional campaigns.
  • Maintain compliance with pharma regulations and company SOPs.
Qualifications & Skills
  • 2–5 years of experience in branded generic pharma sales.
  • Strong communication, negotiation, and interpersonal skills.
  • Familiarity with Delhi NCR pharma market and distribution networks.
  • Ability to work independently and meet targets under pressure.
Compensation & Benefits
  • Competitive salary with performance-based incentives.
  • Travel allowance and other benefits as per company policy.
Apply for this Role

Regulatory Affairs Manager

Location: Haridwar | Experience: Minimum 10 years
▾
About the job

We are looking for an experienced and dynamic Regulatory Affairs Manager to join our pharmaceutical manufacturing facility in Haridwar. The ideal candidate should possess strong expertise in global regulatory requirements, dossier management, and coordination with international regulatory authorities.

This role is ideal for professionals who thrive in a fast-paced regulated environment and have hands-on exposure to international markets.

Key Responsibilities

• Preparation, review, compilation, and submission of regulatory dossiers for global markets.
• Handling CTD/eCTD submissions, variations, renewals, and responses to regulatory queries.
• Coordination with cross-functional departments including QA, QC, Production, R&D, and Business Development.
• Regulatory support for product registrations in semi-regulated and regulated markets.
• Review of artworks, packaging materials, and product-related regulatory documentation.
• Tracking updates in international regulatory guidelines and ensuring compliance.
• Supporting audits, inspections, and customer regulatory requirements.

Desired Candidate Profile

• B.Pharm (Bachelor of Pharmacy)
• M.Pharm (especially Pharmaceutics, Pharmacology, QA, Regulatory Affairs)
• Minimum 10 years of experience in Pharmaceutical Regulatory Affairs.
• Strong exposure to global markets including ROW, Africa, CIS, LATAM, ASEAN, EU, or other regulated/semi-regulated markets.
• Good understanding of CTD/eCTD formats and international regulatory requirements.
• Excellent communication, coordination, and documentation skills.
• Ability to independently manage multiple projects and timelines.

What We Offer

• Opportunity to work with an expanding global pharmaceutical organization.
• Exposure to international regulatory projects and markets.
• Professional growth in a compliance-driven environment.
• Competitive salary and performance-based growth opportunities.

Apply for this Role







    Attach CV