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LIAISONING MANAGER

Location: Shimla, Himachal Pradesh  

Industry: Real Estate & Infrastructure Development

Experience: 3–8 Years

Employment Type: Full-Time

About Us

Taradevi‘s Enclave is promoted by a group of investors and first-generation entrepreneurs, all of whom are ex-corporate professionals and bankers. The promoters have curated multiple sites across Shimla and other parts of North India with an aggregate development potential of a couple of million square feet.

With a vision to launch a new project every six months, Taradevi‘s Enclave is building a high-performing team across functions and levels to support its ambitious growth plans.

Job Overview

We are looking for an experienced and result-oriented Liaisoning Manager to manage government approvals, statutory compliances, regulatory clearances, and stakeholder coordination for our real estate and infrastructure projects. The ideal candidate should possess strong knowledge of government procedures, approval processes, documentation management, and relationship-building with various authorities.

Key Responsibilities

Liaising with Government Departments, Regulatory Authorities, and Private Agencies

Managing approvals and clearances from TCP, Municipal Corporation, Revenue Department, Pollution Control Board, Fire Department, Electricity Board, Jal Shakti Department, PWD, Mining Department, and other statutory bodies

Obtaining and tracking CTE, CTO, Fire NOCs, Environmental Clearances, Building Plan Approvals, Occupancy Certificates, and other project-related permissions

Screening and verification of project-related documents and maintaining records

Managing online registrations, applications, and submissions through government portals

Tracking approval status and ensuring timely follow-up with concerned authorities

Coordinating with CRM, Legal, Engineering, Sales, and Project Teams for smooth project execution

Maintaining proper documentation, compliance records, licenses, and renewal schedules

Building and maintaining strong relationships with government officials and key stakeholders

Handling tender documentation, proposal preparation, bid submissions, and compliance reviews when required

Supporting management in resolving regulatory issues and ensuring project compliance

Desired Candidate Profile

3–8 years of experience in Liaisoning, Government Relations, Regulatory Compliance, or Real Estate Approvals

Strong understanding of statutory approval processes and government procedures

Excellent communication, negotiation, and relationship management skills

Ability to handle multiple stakeholders and manage approvals independently

Experience in Real Estate, Infrastructure, Construction, or Government Projects preferred

Familiarity with Himachal Pradesh government departments and approval frameworks will be an added advantage

Key Skills

• Government Liaisoning

• Regulatory Compliance

• Statutory Approvals & NOCs

• Documentation Management

• Stakeholder Coordination

• Tender Management

• Project Clearances

• Relationship Management

• Negotiation & Communication Skills

Why Join Us?

Opportunity to work on landmark real estate developments

Fast-growing organization with strong expansion plans

Dynamic work environment and career growth opportunities

Direct exposure to large-scale residential and infrastructure projects

Apply Now:

Contact:

️ We're Hiring | Senior Accountant – Real Estate | Shimla / Delhi

About Us

Taradevi's Enclave is promoted by a group of investors and first-generation entrepreneurs, all of whom are ex-corporate professionals and bankers. The promoters have curated multiple sites across Shimla and other parts of North India with an aggregate development potential of a couple of million square feet.

With a vision to launch a new project every six months, Taradevi's Enclave is building a high-performing team across functions and levels to support its ambitious growth plans.

Position: Senior Accountant

We are looking for a seasoned Accountant with proven experience in the real estate sector to manage the financial and accounting functions of our projects. The ideal candidate will possess strong expertise in project accounting, statutory compliance, taxation, financial reporting, and cash flow management.

Key Responsibilities

• Manage end-to-end accounting and bookkeeping functions.
• Maintain project-wise accounts, budgets, and expenditure tracking.
• Prepare monthly MIS reports, financial statements, and management reports.
• Ensure compliance with GST, TDS, Income Tax, and other statutory requirements.
• Handle bank reconciliations, vendor payments, customer receivables, and cash flow monitoring.
• Coordinate with auditors, consultants, banks, and regulatory authorities.
• Monitor project costs and support budgeting and forecasting activities.
• Implement financial controls and ensure compliance with company policies and procedures.

Desired Candidate Profile

• Bachelor's/Master's degree in Commerce, Accounting, or Finance.
• CA, CMA, CA Inter, or equivalent qualification preferred.
• Minimum 8–15 years of experience in accounting and finance, preferably in real estate, construction, or infrastructure projects.
• Strong understanding of project accounting, taxation, and financial reporting.
• Proficiency in Tally, ERP systems, and Microsoft Excel.
• Strong analytical, communication, and organizational skills.

What you'll own:

Project-wise accounts, budgets & cost tracking

GST, TDS & statutory compliance

MIS reports, cash flow & financial statements

Vendor payments, receivables & bank reconciliations

Coordination with auditors, banks & consultants

What you bring:

B.Com / M.Com / CA / CMA / CA Inter

8–15 years in accounting — real estate or construction preferred

Tally, ERP & Excel proficiency

Shimla, HP / Delhi | Full-Time

Apply:

If this isn't for you but you know someone — a share goes a long way!

Responsibility:

• Cooperate with regional sales and local distributor; improve the satisfaction of end-user;
• Responsible for regional technical support (on-line or on-site), make sure the Maglumi system works properly, improve the satisfaction of distributor and end-user;
• Promote the reagent parameters and improve the reagent consumption per analyzer;
• Collect the Maglumi installation information, and establish relationship and follow up the reference customers;
• Give service training to local engineers and establish relationship with engineers from different distributor, keep on guiding and improving their technical skills;
• Apply reagent and spare parts for regional distributor and return the corresponding spare parts in time and follow up the complains;
• Other tasks needed from Snibe

Requirements：

• More than 5 years’ experience worked in IVD area, have strong technical skills, ability to work independently and perform well under pressure;
• Immunoassay experience is more preferred
• Able to use English as working language.

Work location:

Hyderabad or Shimla

Key Responsibilities

• Ensure compliance with cGMP, data integrity, and regulatory requirements.
• Manage Analytical Method Transfer (AMT), Validation (AMV), and Verification activities.
• Review and approve AMT/AMV protocols, reports, and related documentation.
• Ensure timely completion of validation, verification, and transfer projects.
• Review and approve analytical reports, records, and laboratory documents.
• Monitor daily laboratory activities and prepare periodic status reports.
• Coordinate with R&D, external laboratories, and customers for smooth project execution.
• Oversee testing at external laboratories where in-house facilities are unavailable.
• Lead investigations related to OOS, OOT, OOE, deviations, change controls, and CAPA.
• Coordinate with QA, RA, Production, EHS, and other cross-functional teams.
• Conduct GMP and technical training programs for laboratory personnel.
• Develop and mentor Officers, Executives, and Chemists.
• Ensure audit readiness and continuous compliance within the laboratory.

Qualification

M.Sc. (Chemistry/Analytical Chemistry) or equivalent.

Experience

10–15 years of experience in Analytical Method Validation (AMV), Method Transfer (AMT), Method Verification, and Quality Control in a regulated pharmaceutical environment.

Key Skills

AMV, AMT, Method Verification, cGMP, Regulatory Compliance, OOS/OOT Investigations, CAPA, Data Integrity, Team Leadership, and Project Management.

Job Purpose

To manage end-to-end project execution for Injectable and Ophthalmic products, ensuring timely development, technology transfer, regulatory filings, validation, and commercial launches through effective cross-functional coordination.

Key Responsibilities

1. Lead project planning, execution, monitoring, closure, and change management activities.
2. Coordinate with R&D, Manufacturing, QA, QC, Regulatory Affairs, Engineering, Supply Chain, and Commercial teams for successful project delivery.
3. Drive technology transfer, scale-up, validation, and commercialization of products for US and other regulated markets.
4. Ensure achievement of project milestones and maintain OTIF (On-Time-In-Full) performance above 95%.
5. Monitor project timelines, identify risks, and implement mitigation plans to ensure timely execution.
6. Conduct project review meetings and provide regular progress updates to senior management and customers.
7. Manage external development, manufacturing, and technology transfer projects with partners, CMOs, and CDMOs.
8. Establish and implement standardized project management processes, governance, and reporting systems.
9. Ensure compliance with GMP requirements, regulatory commitments, quality standards, and customer agreements.
10. Drive annual filing, validation, and commercialization targets aligned with business objectives.
11. Build and develop a high-performing project management team and support organizational capability development.
12. Escalate critical project and resource issues in a timely manner and drive resolution through cross-functional collaboration.

Qualification & Experience

• B.Pharm / M.Pharm
• 8–12 years of experience in Project Management, Technology Transfer, Product Development, or Operations in Injectable/Ophthalmic formulations.
• Experience in managing projects for USFDA and other regulated markets.

Key Competencies

• Project Management
• Technology Transfer
• Stakeholder Management
• Risk Management
• Regulatory & GMP Compliance
• Leadership & Team Management
• Communication & Problem Solving

Key Responsibilities

Technical Operations & Process Excellence

• Lead scale-up, engineering batches, PPQ batches, process validation, and technology transfer activities.
• Review and approve validation protocols, reports, and batch manufacturing records.
• Drive process optimization, troubleshooting, revalidation, batch size changes, equipment changes, and alternate vendor development.
• Act as SME for process-related deviations, OOS, CAPA, change controls, and investigations.
• Ensure effective risk assessments and continuous process improvement initiatives.
• Support facility and equipment qualification activities.

Manufacturing Network Strategy & Planning

• Lead capacity planning and RCCP activities to align demand with manufacturing capabilities.
• Identify manufacturing constraints and implement mitigation plans.
• Review forecasts, production schedules, and site commitments to ensure timely product supply.
• Drive production scheduling, resource utilization, and schedule adherence.
• Support new product introductions, site transfer projects, and area change validations.
• Lead implementation and optimization of scheduling and planning systems.

Cross-Functional Leadership

• Collaborate with Production, QA, QC, Supply Chain, Engineering, Regulatory Affairs, and R&D teams.
• Drive successful commercialization and lifecycle management of products.
• Review historical manufacturing and quality data to identify improvement opportunities.
• Monitor project progress and ensure on-time delivery from development to commercial launch.

Team Development & Compliance

• Build and develop a high-performing MSAT team.
• Conduct technical training for Production, IPQA, and cross-functional teams.
• Ensure compliance with cGMP, regulatory requirements, and data integrity standards.

Qualification & Experience

• M.Pharm or equivalent.
• 15+ years of experience in pharmaceutical manufacturing, MSAT, technology transfer, and process validation.
• Strong experience in Solid Oral Dosage manufacturing and regulated markets.

Key Competencies

• Technology Transfer & Commercialization
• Process Validation & Lifecycle Management
• OSD Manufacturing
• Capacity Planning & Manufacturing Strategy
• Quality Risk Management
• Regulatory Compliance
• Project & Stakeholder Management
• Leadership & Team Development