Hikal Limited has announced multiple career opportunities for experienced professionals in its Quality and Regulatory Affairs departments. The company is inviting applications from qualified and experienced candidates for various managerial and executive-level positions.

This is an excellent opportunity for pharmaceutical and chemical industry professionals with expertise in regulatory compliance, quality management systems, analytical testing, validation, documentation, and laboratory operations.

Hikal aims to build a healthier and safer world through quality products, innovation, and sustainable practices.

Hikal Recruitment 2026 – Job Details

• Company Name: Hikal Limited
• Industry: Pharmaceutical & Chemical Manufacturing
• Recruitment Type: Experienced Professionals
• Job Location: Not specified in the recruitment advertisement
• Departments: Regulatory Affairs, Quality Assurance and Quality Control
• Application Mode: Email
• Official Website: www.hikal.com

1. Regulatory Affairs Department

Position: Assistant Manager
Experience Required: 6–8 Years

Key Skills and Responsibilities:

• DMF and Dossier Filing
• CTD/eCTD Documentation
• Regulatory Submissions
• Product Lifecycle Management
• Regulatory Compliance
• Amendment and Variation Management
• Authority and Customer Query Responses
• Technical Document Review
• Cross-functional Coordination
• Communication and Documentation Skills

2. Quality Assurance Department

Position: Manager
Experience Required: 12–15 Years

Key Skills and Responsibilities:

• Regulatory Compliance
• Quality Management Systems (QMS)
• Audit and Inspection Management
• Validation and Qualification
• Risk Management
• CAPA and Change Control
• Regulatory Intelligence
• Team Leadership
• Quality Metrics and Reporting
• Continuous Improvement and Compliance Excellence

3. Quality Assurance – Compliance Department

Position: Executive
Experience Required: 6–8 Years

Key Skills and Responsibilities:

• Corporate Compliance Management
• Internal Audit Handling
• Quality Management System (QMS)
• Quality Metrics Preparation and Analysis
• Compliance Gap Assessment and Closure
• Regulatory Compliance Monitoring
• Quality Control (QC) Operations Knowledge (Mandatory)
• CAPA and Compliance Follow-up
• Documentation and Reporting
• Root Cause Analysis and Problem Solving

4. Quality Control Department

Position: Executive
Experience Required: 6–8 Years

Key Skills and Responsibilities:

• HPLC and GC Analysis
• Wet Laboratory Analysis
• Raw Material, In-Process and Finished Product Testing
• Stability Sample Analysis
• Analytical Method Validation and Transfer (AMV/AMT)
• OOS, OOT and Deviation Investigation
• CAPA Implementation
• QC Documentation and SOP Compliance
• Data Review and Technical Reporting
• Instrument Calibration and Maintenance
• cGMP, GLP and Data Integrity Compliance
• Change Control Management
• Stability Data Review and Reporting
• Regulatory and Pharmacopoeial Knowledge
• EHS Compliance and Safety Awareness
• Audit Readiness and Documentation Support

5. Quality Control Department

Position: Manager
Experience Required: 12–15 Years

Key Skills and Responsibilities:

• Quality Control Laboratory Management
• API Testing and Analytical Techniques
• HPLC, GC, UV, IR and Wet Chemistry Analysis
• Stability Study Management
• OOS, OOT and Deviation Investigation
• CAPA and Change Control Management
• Method Validation and Method Transfer
• Data Integrity (ALCOA+) Compliance
• cGMP and GLP Compliance
• Regulatory Audit Management (USFDA, EMA, MHRA and WHO)
• Quality Management Systems (QMS)
• Laboratory Compliance and Documentation
• Instrument Qualification and Calibration
• Team Leadership and People Management
• Root Cause Analysis and Problem Solving
• Regulatory Inspection Readiness

6. Quality Control Department

Position: Assistant Manager
Experience Required: 8–10 Years

Key Skills and Responsibilities:

• HPLC, GC and Instrument Handling
• Wet Chemical Analysis
• Raw Material, Intermediate and API Testing
• Quality Control Documentation
• cGMP and GLP Compliance
• Stability Sample Analysis
• OOS/OOT Investigation Support
• Laboratory Data Integrity (ALCOA+)
• Method Validation and Method Transfer Support
• Calibration and Maintenance Coordination
• SOP, STP and Specification Compliance
• Analytical Troubleshooting
• QMS Awareness (Deviation, CAPA and Change Control)
• Regulatory Compliance and Audit Readiness
• Good Documentation Practices (GDP)

How to Apply for Hikal Recruitment 2026?

Interested and eligible candidates can apply by sharing their updated CV through email.

Application Email: dhanya_br@hikal.com

Candidates should mention the relevant position and department in the email subject line and submit an updated resume highlighting their relevant pharmaceutical or chemical industry experience.

Important: Candidates should verify the job location, qualification requirements and other employment details with the recruitment team before proceeding.

Official Website: https://www.hikal.com/

5 Technical Frequently Asked Questions (FAQs)

1. What experience is required for Hikal Quality Control recruitment?

Hikal is hiring experienced Quality Control professionals for Executive, Assistant Manager and Manager positions. The required experience ranges from 6–8 years for Executive, 8–10 years for Assistant Manager and 12–15 years for Manager.

2. What analytical instruments and techniques are important for Quality Control positions?

Candidates should have practical knowledge of HPLC, GC, UV, IR and wet chemical analysis. Experience in API testing, raw material testing, finished product testing, stability studies and analytical method validation is also important.

3. What is ALCOA+ in pharmaceutical quality control?

ALCOA+ represents the principles of data integrity: Attributable, Legible, Contemporaneous, Original and Accurate, along with additional principles such as Complete, Consistent, Enduring and Available. It ensures reliable and traceable laboratory records.

4. What are the major responsibilities of Regulatory Affairs professionals at Hikal?

Regulatory Affairs professionals are responsible for DMF and CTD/eCTD documentation, regulatory submissions, product lifecycle management, regulatory compliance, amendments, variations and responding to regulatory authority queries.

5. What knowledge is required for Quality Assurance and Compliance positions?

Candidates should have knowledge of cGMP, QMS, internal audits, regulatory inspections, CAPA, deviation management, change control, risk assessment, validation and documentation practices. Leadership and problem-solving skills are also important for managerial positions.

Disclaimer: This recruitment information is prepared based on the shared Hikal recruitment advertisement. Job availability, eligibility criteria, location and other details should be confirmed with the company before applying.