Leben Life Sciences Hiring QA Sr. Officer

QA Sr. Officer Opening

Apply for Sr. Officer QA (Documentation/QMS) at Leben Life Sciences, Akola. M.Pharm with 2–4 yrs experience preferred.

Leben Life Sciences is hiring an experienced Quality Assurance professional for its EU-GMP–approved OSD and semi-solid formulation facility in Akola. This opening is ideal for candidates with strong exposure to documentation control, QMS activities, and regulatory-compliant pharmaceutical manufacturing. With over four decades in the industry, Leben offers a stable environment, structured QA systems, and opportunities to grow within global-standard operations.

Company Overview

Leben Life Sciences Pvt. Ltd. (LLS) is a well-established pharmaceutical formulation manufacturer known for its commitment to responsible healthcare. The company operates a modern EU-GMP–approved plant specializing in oral solid dosage (OSD) and semi-solid formulations. With robust quality systems, global compliance standards, and an experienced leadership team, Leben continues to expand its footprint across regulated and semi-regulated markets.

The organization follows high benchmarks for documentation integrity, QMS performance, audit readiness, and continuous quality improvement—making it an excellent workplace for QA professionals who prioritize compliance and technical excellence.

Job Role & Responsibilities

The Sr. Officer – QA (Documentation/QMS) will handle key quality system functions essential for regulatory compliance and product quality. Responsibilities include:

• Managing controlled documents such as SOPs, specifications, and protocols.
• Maintaining QMS elements including deviations, CAPA, change control, and document issuance.
• Preparing and updating quality metrics, logs, and QMS trackers.
• Supporting internal audits, external audits, and regulatory inspections.
• Ensuring data integrity and adherence to EU-GMP documentation standards.
• Coordinating with Production, QC, and R&D teams for timely documentation closure.
• Assisting in process improvements and QMS enhancement initiatives.

Eligibility / Qualifications

• Education: M.Pharm (Quality Assurance, Pharmaceutics, Pharmaceutical Technology)
• Experience: 2–4 years in pharmaceutical QA (Documentation/QMS preferred)
• Strong understanding of EU-GMP, WHO-GMP, and regulated documentation requirements.
• Hands-on experience with QMS modules (deviations, CAPA, change control).
• Good communication, documentation accuracy, and cross-functional coordination skills.

Relevant Courses: M.Pharm QA, M.Pharm Pharmaceutics, PG Diploma in Quality Management, Certification in QMS/Documentation.

Location & Salary

• Location: Akola, Maharashtra
• Salary: As per company standards and candidate experience
• Facility: EU-GMP Approved OSD & Semi-solid Manufacturing Unit

Application Process

Interested male candidates may submit their updated CV to:

career@lebenlifesciences.com

For queries, contact: 7498035480

Subject Line: Application – Sr. Officer QA (Documentation/QMS) – Akola

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FAQs

Is this role limited to male candidates?
Yes. As per the hiring update, only male candidates are being considered.

Is experience in EU-GMP facilities required?
Preferred, but strong documentation/QMS experience in regulated plants is acceptable.

Are freshers eligible?
No. Minimum 2 years QA experience is mandatory.

What is the main focus of this QA role?
Documentation control, QMS management, and regulatory compliance.

Is this a corporate or plant-based role?
This is a plant-based QA role at the Akola manufacturing facility.

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Summary Table

Category	Details
Company	Leben Life Sciences Pvt. Ltd.
Vacancies	Sr. Officer – QA (Documentation/QMS)
Required Education	M.Pharm
Experience	2–4 years QA Documentation/QMS