Officer - EHS

Drlogy Technologies Pvt. Ltd.

Valsad District

Vor Ort

INR 600.000 - 1.000.000

Vollzeit

14 Tage+

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Zusammenfassung

Olive PharmaScience Ltd in Vapi, Gujarat, seeks an Officer – EHS to implement and monitor environmental, health and safety programs in a cGMP pharmaceutical setting. You will conduct inspections, identify hazards, support risk assessments, investigate incidents, and maintain EHS documentation.

The role requires 3-4 years of EHS experience, diploma/BE with ADIS/PGDIS, and willingness to work on-site. You will coordinate with production, engineering, HR, and others, and lead safety training and

Qualifikationen

  • 3-4 years of EHS experience in pharma or manufacturing.
  • Diploma or BE with relevant ADIS/PGDIS qualifications.
  • Willingness to work on-site in Vapi, Gujarat.

Aufgaben

  • Implement EHS policies and safety programs.
  • Conduct safety inspections and audits.
  • Identify hazards and recommend corrective actions.
  • Support risk assessments and JSA activities.
  • Maintain EHS records, permits, and reports.
  • Coordinate safety training and PPE usage.
  • Coordinate with Production, Engineering and HR on EHS matters.
  • Prepare periodic EHS performance reports.

Kenntnisse

EHS knowledge
Hazard identification
Safety inspections
Training & awareness

Ausbildung

Diploma
B.E. + ADIS
PGDIS

Jobbeschreibung

Job Requirements

Experience: 3 - 4 Years Experience

Education:

  • Diploma
  • B.E. + ADIS
  • PGDIS

All Gender

Vacancy: 1

Last Date to Apply: 12, April 2027

Job Role

Work Location: Vapi

Work Mode: Work From Office

Department: EHS

Role: Officer

Employment type:

  • Full time
Key Skills

Department: EHS. Role-specific duties typical for Officer within EHS in a cGMP-regulated pharmaceutical manufacturing environment. Preference: Exposure in Solid Oral Dos

Preference Languages

Any Language

Job Description

An Officer - EHS (Environment, Health, and Safety) is responsible for implementing and monitoring environmental, occupational health, and workplace-safety practices within the organization. The includes conducting safety inspections, identifying hazards, supporting risk assessments, investigating incidents, coordinating safety training, maintaining EHS documentation, and ensuring compliance with applicable environmental and safety regulations.

  • Implement EHS policies, procedures, and safety programs.
  • Conduct routine workplace safety inspections and audits.
  • Identify workplace hazards and recommend appropriate corrective actions.
  • Support risk assessments and job safety analysis activities.
  • Monitor compliance with environmental, health, and safety requirements.
  • Investigate accidents, incidents, near misses, and unsafe conditions.
  • Maintain EHS registers, reports, permits, and compliance documentation.
  • Conduct employee safety awareness and training programs.
  • Monitor the proper use of personal protective equipment (PPE).
  • Coordinate fire-safety inspections and emergency evacuation drills.
  • Support emergency preparedness and response activities.
  • Monitor waste segregation, handling, and disposal practices.
  • Ensure safe handling, storage, and use of chemicals and hazardous materials.
  • Monitor permit-to-work procedures for activities such as hot work, confined-space entry, and work at height, where applicable.
  • Coordinate with Production, Engineering, Utilities, HR, and other departments on EHS matters.
  • Monitor housekeeping, workplace hygiene, and safe working conditions.
  • Track corrective and preventive actions and follow up on closure.
  • Support environmental monitoring and statutory compliance activities.
  • Participate in internal audits, external inspections, and regulatory reviews.
  • Prepare periodic EHS performance reports and safety statistics.
  • Promote employee participation in safety initiatives and hazard reporting.
  • Ensure compliance with applicable environmental and workplace-safety laws.
  • Follow organizational EHS procedures and continuous-improvement requirements.

Olive PharmaScience Ltd is a research-driven pharmaceutical manufacturing company specializing in the development and production of customized pharmaceutical formulations, over-the-counter (OTC) products, dietary supplements, and soft gelatin dosage forms. With a strong focus on innovation, quality, and global healthcare needs, the company serves pharmaceutical partners and healthcare markets across the world.

As a fully integrated pharmaceutical organization, Olive PharmaScience combines advanced manufacturing capabilities, scientific expertise, and regulatory excellence to deliver high-quality healthcare solutions that improve patient outcomes and support global wellness initiatives.

Our Story

For more than five decades, Olive PharmaScience has been dedicated to advancing pharmaceutical innovation through the development of specialized formulations and healthcare products. The company has built its reputation on a commitment to quality, scientific excellence, and customer-focused manufacturing solutions.

Over the years, Olive PharmaScience has expanded its capabilities through investments in research, advanced manufacturing technologies, and international regulatory compliance. Today, the company is recognized for its expertise in soft gelatin formulations and its ability to deliver customized pharmaceutical solutions for global healthcare markets.

Our Mission

To develop and manufacture innovative, high-quality pharmaceutical and healthcare products that enhance patient well-being and support better healthcare outcomes worldwide.

Key mission priorities include:

Delivering high-quality pharmaceutical formulationsAdvancing innovation through scientific researchSupporting global healthcare accessibilityMaintaining stringent quality and compliance standardsBuilding long-term partnerships with healthcare organizationsEnhancing patient care through effective dosage technologies

Our Vision

To be a trusted global pharmaceutical partner recognized for innovation, quality, scientific excellence, and advanced healthcare solutions that improve lives worldwide.

Our Services / What We Offer

Olive PharmaScience offers a comprehensive range of pharmaceutical development and manufacturing services, including:

Soft Gelatin Capsule ManufacturingPharmaceutical Formulation DevelopmentCustomized Pharmaceutical ProductsOver-the-Counter (OTC) ProductsDietary SupplementsNutraceutical ProductsContract Development and Manufacturing Services (CDMO)Product Licensing SolutionsRegulatory Support ServicesGlobal Pharmaceutical Supply Solutions

The company serves diverse healthcare categories, including:

Generic PharmaceuticalsOTC Healthcare ProductsNutritional SupplementsHigh-Potency MoleculesHormonal ProductsOncology ProductsImmunosuppressants

Why Choose UsMore than five decades of pharmaceutical expertiseSpecialized focus on soft gelatin dosage formsFully integrated pharmaceutical manufacturing capabilitiesStrong research and development infrastructureInternational regulatory approvals and certificationsGlobal market presence and partnershipsCustomized product development solutionsCommitment to quality, innovation, and complianceAdvanced manufacturing technologiesCustomer-centric approach to pharmaceutical development

Our Team

Olive PharmaScience is supported by a team of pharmaceutical scientists, researchers, quality specialists, regulatory professionals, manufacturing experts, and business leaders who work together to deliver innovative healthcare solutions.

The organization promotes a culture of continuous learning, scientific excellence, collaboration, and innovation, enabling teams to address evolving healthcare challenges and market requirements effectively.

Infrastructure / Technology

Olive PharmaScience operates three state-of-the-art manufacturing facilities in India designed to meet international current Good Manufacturing Practice (cGMP) standards. These facilities support large-scale pharmaceutical manufacturing while ensuring quality, efficiency, and regulatory compliance.

Key infrastructure strengths include:

Soft Gelatin Manufacturing FacilitiesPharmaceutical Development LaboratoriesResearch and Development CentersQuality Control LaboratoriesAdvanced Analytical SystemsRegulatory Documentation SupportInternational Supply Chain CapabilitiesScalable Manufacturing Infrastructure

The company is also expanding its capabilities with GMP-approved gummy manufacturing facilities for nutritional and pharmaceutical OTC products.

Quality & Compliance

Quality remains a cornerstone of Olive PharmaScience's operations. The company follows stringent manufacturing, testing, and quality assurance practices to ensure product safety, efficacy, and consistency.

Its regulatory approvals and certifications include:

US FDAWHO-GMPEU GMPTGA AustraliaRegulatory approvals across multiple international markets

These standards support the company's ability to serve highly regulated pharmaceutical markets worldwide.

Innovation is central to Olive PharmaScience's growth strategy.

Through continuous investment in research and product development, Olive PharmaScience strives to create differentiated healthcare solutions that meet the evolving needs of patients and healthcare providers globally.

Our Commitment

Olive PharmaScience is committed to improving healthcare through scientific innovation, manufacturing excellence, and responsible business practices. The company continuously invests in technology, quality systems, and talent development to ensure reliable healthcare solutions for global markets.

Guided by its commitment to quality, innovation, and patient well-being, Olive PharmaScience aims to build lasting partnerships while contributing to a healthier future for communities around the world.

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