Career @Accuprec

Manage engineering stores and warehouse operations, ensuring accurate inventory control, material traceability, and efficient stock management.

• Handle engineering stores, warehouse and inventory operations
• Manage material receipt, inspection, storage and issuance
• Maintain inventory control and accurate stock records
• Prepare GRN/GRM and update stock entries
• Ensure material identification, labeling, traceability and accountability
• Maintain engineering store operations and inventory accuracy

Contribute to cutting-edge R&D projects in nanomaterial synthesis, formulation, and characterization using advanced analytical instruments.

• Work on R&D projects involving synthesis, formulation, analysis and commercialization of materials
• Perform nanomaterial characterization using advanced instruments
• Interpret NMR, EPR, XRD, AFM, CRYO TEM and SEM data
• Identify niche API/KSM through market, patent and technology-landscape searches
• Support lab-scale and pilot-scale setup activities

Experienced pharmaceutical formulation researcher to support and lead development activities within the FD department.

Handle store and purchase operations, supporting procurement, inventory management, and supply chain activities.

Support IT operations and pharma-specific systems, ensuring technology infrastructure aligns with regulatory and business requirements.

Drive end-to-end recruitment processes to attract and onboard top talent across departments in a fast-paced pharma research environment.

Manage front desk operations, visitor management, and administrative support to ensure a professional and efficient office environment.

Lead civil engineering projects, oversee construction and maintenance activities, and ensure compliance with safety and quality standards.

Oversee environment, occupational health, and safety operations to maintain regulatory compliance and a safe working environment.

Perform hands-on technical maintenance, troubleshooting, and operational support for engineering systems and equipment.

Support mechanical research and development activities, contributing to design, testing, and analysis of engineering solutions.

Support quality assurance unit operations, ensuring compliance with GMP/GLP standards and maintaining documentation and audit readiness.

Provide administrative and operational support within the TICO department, ensuring smooth day-to-day office functioning.

Provide general administrative and clerical support to ensure efficient office operations across departments.

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

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

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

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

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