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TFP Pharma

Ahmedabad, Gujarat

Department: Quality Control

Experience: 2-5 Years

Industry: Pharmaceutical

Education: MSc

Remarks: ADL department

Job Description

Officer ADL – Quality Control | TFP Pharma | Ahmedabad, Gujarat, India

TFP Pharma is hiring qualified professionals for the role of Officer ADL for its pharmaceutical analytical development operations located in Ahmedabad, Gujarat, India. This full-time opportunity is suitable for candidates with 2 to 5 years of experience in analytical development laboratory operations, pharmaceutical quality control systems, laboratory documentation, analytical testing, instrument handling, and compliance activities within regulated pharmaceutical environments. Candidates having experience in ADL department operations will be preferred. The selected candidate will support analytical development activities, maintain laboratory documentation, perform analytical testing procedures, coordinate with quality and R&D teams, ensure adherence to GMP practices, and support laboratory operational efficiency. This role offers valuable exposure to pharmaceutical analytical systems, laboratory quality environments, compliance-driven workflows, and scientific testing operations focused on analytical accuracy, documentation quality, process reliability, and regulatory adherence.

Location

Ahmedabad, Gujarat, India

Employment Type

Full-time

Experience Required

2 to 5

Compensation & Benefits

Competitive salary package with exposure to pharmaceutical analytical systems, laboratory operations, and long-term professional growth opportunities.

About TFP Pharma

TFP Pharma operates in the pharmaceutical industry specializing in regulated manufacturing systems, healthcare products, and analytical laboratory operations.

Position Overview

The Officer ADL will support analytical development laboratory activities, pharmaceutical testing systems, and quality documentation processes.

Key Responsibilities

  • Perform analytical testing and laboratory support activities.
  • Maintain laboratory records and analytical documentation.
  • Coordinate with quality control and R&D teams.
  • Support instrument handling and laboratory operations.
  • Ensure adherence to GMP and laboratory quality standards.
  • Participate in analytical reviews and technical discussions.
  • Monitor laboratory workflow and process compliance.
  • Support data compilation and reporting activities.
  • Maintain operational discipline within laboratory systems.
  • Assist in continuous improvement and quality enhancement initiatives.

Required Skills & Competencies

  • Strong understanding of analytical laboratory systems.
  • Knowledge of pharmaceutical quality control operations.
  • Laboratory documentation and reporting abilities.
  • Problem-solving and analytical thinking capabilities.
  • Communication and coordination skills.
  • Awareness of GMP and pharmaceutical compliance standards.
  • Attention to analytical accuracy and laboratory quality.
  • Time management and multitasking abilities.
  • Instrument handling and laboratory coordination capabilities.
  • Adaptability to regulated pharmaceutical environments.

Educational Qualification

MSc

About the Industry

The pharmaceutical analytical development industry depends on advanced laboratory systems, analytical testing processes, and compliance-driven operations to ensure product quality and scientific reliability.

Why Join TFP Pharma?

TFP Pharma offers professionals opportunities to work in advanced pharmaceutical laboratory environments with exposure to analytical development systems and quality operations.

How to Apply

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