Mendine Pharmaceuticals Hiring Senior Technical Officer – Quality Assurance

Mendine Pharmaceuticals Hiring Senior Technical Officer – Quality Assurance in Kolkata (5–8 Years Experience)

Mendine Pharmaceuticals Pvt. Ltd. is hiring for the position of Senior Technical Officer – Quality Assurance (QA Executive level) at its manufacturing facility in Kolkata, West Bengal. This opportunity is open to experienced pharmaceutical professionals with 5 to 8 years of experience in Quality Assurance within a regulated pharma environment. The role focuses on ensuring compliance with GMP standards, quality management systems, regulatory audits, and documentation control.

This position is ideal for M.Pharm and B.Pharm professionals seeking mid-level leadership roles in pharmaceutical quality assurance, regulatory compliance, and audit management within a growing pharma manufacturing organization.

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Company Overview

Mendine Pharmaceuticals Pvt. Ltd. is a pharmaceutical manufacturing company committed to delivering high-quality, compliant, and affordable healthcare products. With a focus on regulatory adherence, robust quality systems, and ethical manufacturing practices, Mendine operates in alignment with national and international pharmaceutical standards.

The organization emphasizes strong documentation practices, validated processes, and structured quality oversight to ensure that every batch manufactured meets defined specifications and regulatory requirements. By maintaining a compliance-driven culture and investing in trained quality professionals, Mendine continues to strengthen its position within the pharmaceutical industry.

Working at Mendine offers professionals hands-on exposure to quality management systems, regulatory inspections, internal audits, and cross-functional coordination across manufacturing, production, and quality control teams.

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Job Role & Responsibilities

The Senior Technical Officer – Quality Assurance will be responsible for maintaining and strengthening quality systems at the pharmaceutical manufacturing facility. The role demands deep knowledge of GMP compliance, QMS documentation, and regulatory expectations.

Quality Assurance & GMP Compliance

• Ensure strict adherence to Good Manufacturing Practices (GMP) across manufacturing operations
• Monitor implementation of Standard Operating Procedures (SOPs)
• Oversee quality documentation to ensure completeness and compliance
• Support continuous improvement of quality management systems (QMS)

Documentation & Record Review

• Review and approve batch manufacturing records and related documentation
• Ensure proper maintenance of logbooks, validation records, and quality documentation
• Support document control systems including SOP revisions and updates
• Maintain data integrity and compliance with regulatory expectations

Audit & Regulatory Support

• Support internal audits and regulatory inspections
• Coordinate with cross-functional teams to address audit observations
• Assist in preparation of corrective and preventive action (CAPA) plans
• Ensure timely closure of audit findings and compliance gaps

Cross-Functional Coordination

• Collaborate with Production, QC, and other departments to ensure quality standards are met
• Provide guidance on quality-related issues and compliance matters
• Support training initiatives related to GMP and documentation practices

Travel & Regulatory Requirements

• Be flexible for travel related to regulatory requirements or inspection support activities
• Represent QA department during interactions with external stakeholders when required

The role requires a proactive approach, analytical thinking, and the ability to manage multiple compliance responsibilities in a regulated pharmaceutical environment.

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Eligibility / Qualifications

This role is intended for experienced pharmaceutical quality professionals with strong compliance knowledge.

Educational Qualifications

M.Pharm, B.Pharm

Experience Requirements

• 5 to 8 years of experience in Quality Assurance within the pharmaceutical industry
• Strong exposure to GMP guidelines and QMS implementation
• Experience in handling internal and external audits

Required Skills

• Strong understanding of GMP, QMS, and regulatory compliance processes
• Good analytical and problem-solving abilities
• Effective written and verbal communication skills
• Strong coordination and teamwork capabilities
• Ability to manage documentation and regulatory timelines

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Location & Salary

Job Location: Kolkata, West Bengal
Department: Quality Assurance
Designation: Senior Technical Officer – QA

Compensation will be suitable and negotiable based on current salary package, experience level, and industry standards. The role offers professional growth within quality assurance and regulatory compliance functions.

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Application Process

Interested and eligible candidates are invited to share their updated CV via email.

Email CV to:
piyali.basu@mendine.com
atrayee.mandal@mendine.com

Company Website:
www.mendine.com

Candidates are advised to mention “Senior Technical Officer – QA” in the subject line while applying.

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Frequently Asked Questions (FAQs)

Who can apply for the QA Executive role at Mendine Pharmaceuticals?
Candidates with M.Pharm or B.Pharm qualification and 5–8 years of Quality Assurance experience can apply.

Is GMP experience mandatory?
Yes. Strong knowledge of GMP and QMS is required.

Does the role involve audit handling?
Yes. The candidate must support internal and external audits.

Is travel required for this role?
Yes. Flexibility to travel for regulatory requirements is expected.

Is the salary fixed?
No. Compensation is negotiable based on current package and industry norms.

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Summary Table

Company	Mendine Pharmaceuticals Pvt. Ltd.
Vacancies	Senior Technical Officer – Quality Assurance
Required Education	M.Pharm, B.Pharm
Experience	5 to 8 Years

Tagged as: pharma jobs in kolkata