At Accuprec Research Labs Pvt. Ltd., we are committed to delivering excellence in pharmaceutical research, analytical development, and regulatory compliance. If you are ready to grow, innovate, and make an impact — explore our current openings below.
Business Development
Business Development Executive
Seeking a proactive Business Development Executive to drive lead generation, client acquisition, and market expansion in the pharma services space.
- Identify and generate new business opportunities through research, networking, and outreach
- Execute cold emailing campaigns and ensure timely follow-ups
- Develop and implement sales and business growth strategies
- Represent the organization at industry events, expos, and conferences
- Conduct market research to understand trends, customer needs, and competitors
- Maintain accurate records of leads, communications, and sales activities
Mechanical
Manager – Mechanical Engineering
Experienced Mechanical Engineering Manager to lead engineering operations, innovation, and project execution with strong technical expertise.
- Lead engineering design, R&D, and technical operations
- Ensure timely execution of projects while maintaining operational efficiency
- Oversee quality systems and ensure regulatory compliance
- Conduct internal audits and represent in technical discussions
- Manage cross-functional engineering teams and leadership initiatives
- Develop long-term strategies for operational excellence and growth
Project Management
Executive / Sr. Executive – Project Management
Coordinate projects, manage client communication, and ensure timely delivery with high quality across cross-functional teams.
- Monitor and track project progress to meet deadlines
- Coordinate with cross-functional teams for smooth execution
- Act as a primary point of contact for clients
- Support project planning and new project setup
- Maintain documentation and prepare detailed reports
Regulatory Affairs
Regulatory Affairs Executive
Hands-on experience in global submissions (CIS/EAEU markets), dossier preparation, compliance management, and regulatory coordination.
- Prepare and submit CTD/eCTD dossiers as per regulatory requirements
- Manage EAEU Unified Registration submissions
- Maintain Site Master File (SMF) and GMP documentation
- Perform gap analysis and ensure dossier compliance
- Track regulatory updates and global guidelines
- Coordinate with R&D, QA, and Production teams
Regulatory Affairs
Regulatory Query Response Officer / Executive
Manage regulatory queries from health authorities and provide scientifically sound, compliant responses within defined timelines.
- Handle and respond to regulatory queries from global authorities
- Prepare technical justifications and supporting documents
- Ensure compliance with regulatory standards
- Coordinate with cross-functional teams
- Implement CAPA (Corrective & Preventive Actions)
- Maintain data integrity and documentation standards
Analytical Development
Study Director
Lead analytical and bioanalytical studies while ensuring compliance with international guidelines and maintaining high data integrity.
- Conduct analytical method validation (ICH Q2)
- Perform chemical characterization studies (ISO standards)
- Execute extractables & leachables (E&L) studies
- Manage bioanalytical and pharmacokinetic studies (ICH M10)
- Review data, protocols, and reports
- Guide junior team members and maintain lab standards
Analytical Development (AD)
Research Associate / Sr. Research Associate (HPLC – AMV)
Strong expertise in analytical method development and validation, with hands-on experience in pharmaceutical analysis using HPLC and related instruments.
- Perform method development, validation, and verification
- Conduct forced degradation studies
- Execute analytical method transfer between labs
- Operate HPLC, UV, Dissolution, and IC instruments
- Prepare reports and documentation as per GMP/GLP
- Troubleshoot analytical issues and provide solutions
