Harman Hiring Lab QA, Regulatory Affairs, EHS and QC Stability

Harman Finochem Hiring QA RA EHS QC Jobs

Harman Finochem hiring for Lab QA, Regulatory Affairs, EHS and QC Stability roles. BSc, MSc, BPharm, MPharm candidates with 6-12 years experience.

Professionals seeking pharmaceutical jobs in Quality Assurance, Regulatory Affairs, Environmental Health & Safety, and Quality Control can explore the latest hiring opportunity announced by Harman Finochem Limited. The company is currently recruiting experienced candidates for its API manufacturing facility and is looking for skilled professionals who can contribute to quality systems, regulatory compliance, safety management, and stability studies.

This recruitment drive is ideal for candidates with experience in API pharmaceutical manufacturing environments and expertise in GMP documentation, regulatory submissions, CAPA management, audit coordination, EHS compliance, stability testing, and quality systems. Immediate joiners are preferred, making this an excellent opportunity for professionals looking for a quick career move in the pharmaceutical industry.

For candidates actively searching for pharmaceutical quality assurance jobs, regulatory affairs careers, GMP compliance jobs, quality control stability jobs, API pharma vacancies, and pharmaceutical safety management opportunities, this hiring announcement offers multiple career growth possibilities within a well-established pharmaceutical organization.

Company Overview

Harman Finochem Limited is a recognized pharmaceutical company engaged in the manufacturing of Active Pharmaceutical Ingredients (APIs). The organization is known for maintaining high-quality manufacturing standards, strong regulatory compliance systems, and a commitment to delivering pharmaceutical products that meet global quality requirements.

The company operates with a focus on quality, innovation, operational excellence, and regulatory adherence. Harman Finochem continues to strengthen its workforce by hiring experienced professionals capable of supporting its quality systems, regulatory functions, safety initiatives, and compliance programs.

Employees at Harman Finochem gain exposure to modern pharmaceutical manufacturing practices, international regulatory standards, and career development opportunities within a professional work environment.

Primary Keyword: Pharmaceutical Regulatory Affairs Jobs

Company Hiring Details

Harman Finochem is currently hiring for the following departments:

• Lab Quality Assurance (Lab QA)
• Regulatory Affairs
• Environment Health & Safety (EHS)
• Quality Control – Stability

Candidates with API pharmaceutical industry experience will be preferred for all positions.

Job Role & Responsibilities

Executive / Senior Executive – Lab QA

The Lab Quality Assurance team plays a critical role in ensuring laboratory compliance, documentation integrity, audit readiness, and adherence to pharmaceutical quality standards.

Key Responsibilities

• Review GMP documentation and laboratory records.
• Ensure compliance with regulatory and quality management systems.
• Manage deviation investigations and corrective actions.
• Coordinate CAPA implementation and effectiveness reviews.
• Handle change control documentation and approvals.
• Support internal and external audits.
• Review quality-related records and compliance reports.

Required Skills

• GMP Documentation
• Quality Management Systems
• CAPA Management
• Change Control
• Audit Coordination
• Regulatory Compliance
• Pharmaceutical Documentation Review

Executive / Senior Executive – Regulatory Affairs

The Regulatory Affairs department is responsible for ensuring that pharmaceutical products meet regulatory requirements across various markets.

Key Responsibilities

• Preparation and review of regulatory dossiers.
• Compilation of pharmaceutical registration documents.
• Regulatory submission management.
• Support compliance activities and regulatory commitments.
• Coordinate with cross-functional teams for documentation requirements.
• Maintain regulatory databases and records.
• Ensure adherence to applicable pharmaceutical regulations.

Required Skills

• Regulatory Documentation
• Dossier Preparation
• Pharmaceutical Registration
• Submission Management
• Regulatory Compliance
• Technical Documentation
• Pharmaceutical Regulations

Deputy Manager – EHS

The Environment Health & Safety department ensures a safe and compliant workplace while supporting sustainable pharmaceutical manufacturing operations.

Key Responsibilities

• Monitor EHS compliance across manufacturing operations.
• Conduct safety audits and inspections.
• Perform risk assessments and hazard identification activities.
• Implement safety improvement programs.
• Ensure statutory compliance requirements are met.
• Support accident prevention and safety awareness initiatives.
• Coordinate regulatory inspections related to safety and environment.

Required Skills

• EHS Compliance
• Safety Audits
• Risk Assessment
• Hazard Identification
• Occupational Safety
• Environmental Compliance
• Statutory Compliance Management

Senior Executive / Assistant Manager – QC Stability

The Quality Control Stability team is responsible for managing stability studies and ensuring compliance with regulatory quality requirements.

Key Responsibilities

• Manage stability study programs.
• Coordinate sample collection and testing schedules.
• Review analytical data and stability reports.
• Ensure compliance with regulatory stability guidelines.
• Maintain accurate documentation and records.
• Support regulatory submissions through stability data generation.
• Participate in quality investigations and compliance reviews.

Required Skills

• Stability Study Management
• Sample Analysis
• Quality Documentation
• Data Review
• Regulatory Compliance
• Pharmaceutical Quality Systems
• Laboratory Documentation

Eligibility / Qualifications

Candidates applying for the available positions should possess the following educational qualifications:

Lab QA

• B.Sc.
• M.Sc.

Regulatory Affairs

• B.Pharm
• M.Pharm
• M.Sc.

EHS

• B.Sc.
• M.Sc.
• Diploma in Safety

QC Stability

• B.Pharm
• M.Pharm
• M.Sc.

Relevant Educational Courses

Bachelor of Science (B.Sc.), Master of Science (M.Sc.), Pharmaceutical Chemistry, Analytical Chemistry, Organic Chemistry, Industrial Chemistry, B.Pharm, M.Pharm, Pharmaceutical Quality Assurance, Regulatory Affairs, Industrial Pharmacy, Diploma in Industrial Safety, Environmental Health & Safety Management, Occupational Safety.

Experience Requirements

Executive / Senior Executive – Lab QA

Experience: 6 to 8 Years

Executive / Senior Executive – Regulatory Affairs

Experience: 6 to 8 Years

Deputy Manager – EHS

Experience: 10 to 12 Years

Senior Executive / Assistant Manager – QC Stability

Experience: 8 to 10 Years

Preferred Candidate Profile

The ideal candidate should possess:

• Experience in API pharmaceutical manufacturing companies.
• Strong understanding of GMP regulations.
• Knowledge of pharmaceutical documentation systems.
• Exposure to audits and compliance activities.
• Strong analytical and problem-solving skills.
• Ability to work in cross-functional environments.

Preference: Immediate joiners will be given first preference.

Location & Salary

Job Location: API Facility, India

Approximate Salary: ₹8 LPA – ₹22 LPA

Compensation may vary depending on experience, current salary, technical expertise, and interview performance.

Application Process

Interested and eligible candidates can apply by sending their updated resume to the official recruitment email.

Email Application

Email ID: Emamad@harmanfinochem.com

Candidates are advised to mention the position applied for in the email subject line for faster processing.

Documents Recommended

• Updated Resume
• Educational Certificates
• Experience Certificates
• Current CTC Details
• Notice Period Information

Why Join Harman Finochem?

Harman Finochem offers professionals an opportunity to work in a regulated API manufacturing environment focused on quality, compliance, and operational excellence.

Benefits of Working with Harman Finochem

• Exposure to global pharmaceutical standards.
• Opportunities in regulatory and quality systems.
• Career growth in API manufacturing.
• Professional and compliance-driven work culture.
• Learning opportunities across multiple pharmaceutical functions.
• Stable and growth-oriented organization.

Frequently Asked Questions (FAQs)

1. What positions are currently available at Harman Finochem?

The company is hiring for Lab QA, Regulatory Affairs, EHS, and QC Stability departments.

2. Is API pharmaceutical experience mandatory?

Yes. Candidates with API pharmaceutical company experience are preferred.

3. Are immediate joiners preferred?

Yes. Immediate joiners will receive priority consideration.

4. What qualification is required for Regulatory Affairs roles?

Candidates with B.Pharm, M.Pharm, or M.Sc. qualifications are eligible.

5. What experience is required for the EHS position?

The Deputy Manager EHS role requires 10 to 12 years of relevant experience.

6. How can candidates apply?

Candidates can send their updated CV to Emamad@harmanfinochem.com.

Summary

Category	Details
Company	Harman Finochem Limited
Department Vacancies	Executive/Sr. Executive – Lab QA, Executive/Sr. Executive – Regulatory Affairs, Deputy Manager – EHS, Sr. Executive/Assistant Manager – QC Stability
Qualification	B.Sc., M.Sc., B.Pharm, M.Pharm, Diploma in Safety
Experience	6–12 Years (Role Dependent)
Location	API Facility