Kaisha Lifesciences Pvt. Ltd. has announced a new job opportunity for experienced pharmaceutical professionals in its Regulatory Affairs Department. The company is inviting applications for the positions of Officer / Senior Officer at its manufacturing facility in Daman.

Candidates with B.Pharm or M.Pharm qualifications and at least 5 years of relevant experience in regulatory submissions, pharmacovigilance, import-export licensing, vendor qualification, and artwork management are encouraged to apply.

About Kaisha Lifesciences Pvt. Ltd.

Kaisha Lifesciences Private Limited is a pharmaceutical company and part of the Dadachanji Group of Companies. The organization is committed to manufacturing safe, high-quality, and effective pharmaceutical medications.

The company also provides contract research and development (R&D) services to other pharmaceutical organizations.

Kaisha Lifesciences focuses on pharmaceutical quality, regulatory compliance, product development, and maintaining industry standards.

Kaisha Lifesciences Recruitment 2026 – Job Details

Company Name: Kaisha Lifesciences Pvt. Ltd.

Department: Regulatory Affairs

Job Positions: Officer / Senior Officer

Educational Qualification: B.Pharm / M.Pharm

Required Experience: 5+ Years

Industry: Pharmaceutical

Job Location: Bhimpore, Daman – 396210, UT of Daman & Diu (as stated in the recruitment notice)

Application Mode: Email Resume

Selection Process: Interview

Available Positions and Eligibility Criteria

Regulatory Affairs – Officer / Senior Officer

Qualification:

• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

Experience: Minimum 5 years of professional experience in relevant pharmaceutical regulatory affairs activities.

Required Professional Experience:

• Regulatory submissions
• Pharmacovigilance
• Import-export licensing
• Vendor qualification
• Pharmaceutical artwork management

Candidates should have practical knowledge of regulatory documentation, pharmaceutical compliance requirements, and regulatory affairs procedures.

Key Roles and Responsibilities

Selected candidates may be responsible for the following activities, depending on their assigned role:

1. Regulatory Submissions

Prepare, review, and coordinate regulatory documentation required for pharmaceutical product registration, approval, and compliance.

2. Pharmacovigilance

Support pharmaceutical drug safety activities, including adverse drug reaction reporting, safety documentation, and compliance with applicable pharmacovigilance requirements.

3. Import-Export Licensing

Handle regulatory documentation and licensing activities associated with pharmaceutical product imports and exports.

4. Vendor Qualification

Participate in vendor qualification activities by reviewing supplier documentation and ensuring compliance with applicable pharmaceutical quality standards.

5. Artwork Management

Review pharmaceutical packaging artwork, labels, cartons, and product information to ensure compliance with approved regulatory requirements.

Required Skills and Knowledge

Candidates should preferably possess:

• Knowledge of pharmaceutical regulatory affairs.
• Understanding of regulatory submission procedures.
• Familiarity with pharmacovigilance requirements.
• Experience handling pharmaceutical import-export documentation.
• Knowledge of vendor qualification procedures.
• Understanding of packaging artwork review and approval.
• Good documentation and communication skills.
• Familiarity with pharmaceutical regulatory guidelines.

Job Location and Company Address

Kaisha Lifesciences Pvt. Ltd.

Survey No. 342/3(77),
Bharat Industrial Estate,
Bhimpore, Daman – 396210,
UT of Daman & Diu (as mentioned in the advertisement).

How to Apply for Kaisha Lifesciences Recruitment 2026

Interested and eligible candidates can apply by sending their updated resumes to the company’s HR department through email.

Application Process:

1. Prepare an updated professional resume.
2. Mention your educational qualifications and relevant pharmaceutical experience.
3. Highlight your experience in regulatory affairs, pharmacovigilance, import-export licensing, vendor qualification, and artwork management.
4. Mention the position applied for: Officer / Senior Officer – Regulatory Affairs.
5. Send your resume to the official recruitment email address.

HR Email ID: hrd@kaishalifesciences.com

Contact Numbers: +91 7574996300 / 400

Note: The recruitment advertisement does not specify an application deadline, interview date, or salary package. Candidates should contact the HR department for further details.

5 Technical Interview FAQs for Regulatory Affairs Department

1. What is the CTD format in pharmaceutical regulatory submissions?

Answer: CTD stands for Common Technical Document. It is a standardized format used for submitting pharmaceutical registration applications to regulatory authorities.

The CTD consists of five modules:

• Module 1: Regional Administrative Information
• Module 2: CTD Summaries
• Module 3: Quality Documentation
• Module 4: Nonclinical Study Reports
• Module 5: Clinical Study Reports

The CTD format helps organize regulatory submissions and supports efficient review by regulatory authorities.

2. What is pharmacovigilance, and why is it important in the pharmaceutical industry?

Answer: Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or other medicine-related problems.

Its major objectives include:

• Monitoring adverse drug reactions (ADRs).
• Identifying potential medicine safety risks.
• Evaluating drug safety information.
• Supporting regulatory safety reporting.
• Improving patient safety.

Pharmacovigilance is essential for continuously monitoring the benefit-risk profile of pharmaceutical products.

3. What documents are generally required for pharmaceutical import-export licensing?

Answer: Pharmaceutical import-export requirements depend on the product, destination country, and applicable regulatory framework.

Common documents may include:

• Import Export Code (IEC).
• Applicable manufacturing or wholesale licenses.
• Product registration or marketing authorization documents.
• Certificate of Pharmaceutical Product (CPP), where required.
• Certificate of Analysis (COA).
• Commercial invoice and packing list.
• Import or export permissions, where applicable.

Candidates should understand the relevant CDSCO, DGFT, and destination-country regulatory requirements.

4. What is vendor qualification in the pharmaceutical industry?

Answer: Vendor qualification is a documented process used to evaluate and approve suppliers of raw materials, packaging materials, and other critical products or services.

The process may include:

• Vendor assessment and risk evaluation.
• Review of quality certifications.
• Evaluation of supplier documentation.
• Vendor audits, where required.
• Material quality assessment.
• Approval and periodic performance monitoring.

Vendor qualification helps ensure that purchased materials and services consistently meet established quality requirements.

5. What is pharmaceutical artwork management, and what are the important regulatory checks?

Answer: Pharmaceutical artwork management involves reviewing and controlling printed packaging information such as labels, cartons, foils, and package inserts.

Important checks include:

• Correct product name and strength.
• Approved composition and dosage information.
• Batch number, manufacturing date, and expiry date fields.
• Storage conditions.
• Required warnings and statutory declarations.
• Manufacturer and marketing authorization details.
• Compliance with approved product information and applicable labeling regulations.

Proper artwork management helps prevent labeling errors, regulatory noncompliance, and potential medication errors.

Why Consider a Career at Kaisha Lifesciences?

Kaisha Lifesciences offers an opportunity for experienced pharmaceutical professionals to work in regulatory affairs within the pharmaceutical industry.

The advertised positions involve important areas such as regulatory submissions, pharmacovigilance, pharmaceutical licensing, vendor qualification, and artwork management.

Professionals with relevant regulatory affairs experience can consider this opportunity to further develop their expertise.

Conclusion

Kaisha Lifesciences Recruitment 2026 presents a career opportunity for B.Pharm and M.Pharm graduates with 5+ years of experience in the pharmaceutical Regulatory Affairs Department.

The company is hiring for Officer and Senior Officer positions at its Daman facility.

Interested candidates who meet the eligibility requirements can send their updated resumes to hrd@kaishalifesciences.com.

Important Disclaimer: This article is based on the recruitment advertisement shared for Kaisha Lifesciences Pvt. Ltd. Candidates are advised to verify vacancy availability, eligibility criteria, interview schedules, and other recruitment details directly with the company before applying. Never pay money for a job application or interview.