Leben Life Sciences Hiring Officer/Sr. Officer – Quality Control (HPLC, GLP)

QC Officer Openings | Leben Life Sciences Akola

Apply for Officer/Sr. Officer – Quality Control (HPLC, GLP) at Leben Life Sciences, Akola. Qualification: M.Sc/B.Pharm/M.Pharm, 2–4 years’ experience.

URL Slug: leben-life-sciences-quality-control

Leben Life Sciences Pvt. Ltd. (LLS), a trusted name in the pharmaceutical formulations industry for over four decades, is inviting applications for the role of Officer/Sr. Officer – Quality Control (HPLC/GLP) at its EU-GMP approved OSD & Semi-Solids formulation facility in Akola, Maharashtra. This opportunity is ideal for candidates with a strong background in HPLC, GLP practices, and quality assurance within regulated pharmaceutical environments.

Company Overview

Leben Life Sciences has earned a strong reputation in the global pharmaceutical sector with its commitment to responsible healthcare, regulatory compliance, and product innovation. With an EU-GMP certified manufacturing facility, the company caters to both domestic and international markets, producing a wide range of oral solid dosage (OSD) forms and semi-solid formulations. LLS stands for quality, trust, and patient-centric healthcare solutions.

Job Role & Responsibilities

As an Officer/Sr. Officer in Quality Control, you will:

• Conduct routine and non-routine analysis of pharmaceutical products using HPLC and other analytical techniques.
• Ensure compliance with GLP (Good Laboratory Practices) and international quality standards.
• Maintain laboratory instruments, logbooks, registers, and documentation systems.
• Support investigations into deviations, OOS (Out-of-Specification) results, and CAPA implementation.
• Assist in method validation, calibration, and stability testing.
• Coordinate with cross-functional teams to ensure timely reporting and resolution of quality-related issues.
• Adhere to company SOPs, QMS (Quality Management System) guidelines, and regulatory requirements.

Eligibility / Qualifications

• Educational Qualification: M.Sc in Chemistry, B.Pharm, or M.Pharm (Pharmaceutical Chemistry, Pharmaceutical Analysis, or related courses).
• Experience: 2–4 years in pharmaceutical Quality Control (HPLC/GLP).
• Skills Required:
  • Proficiency in HPLC operation and troubleshooting.
  • Strong knowledge of GLP, cGMP, and regulatory compliance.
  • Experience with stability studies, method validation, and technical documentation.
  • Good communication and problem-solving abilities.

Location & Salary

• Location: Akola, Maharashtra, India
• Salary: Competitive, as per industry standards.

Application Process

Eligible candidates may apply by sending their updated resume to the official email address:

Email: career@lebenlifesciences.com
Contact: 7498035480
Website: www.lebenlifesciences.com

Apply before 23rd August 2025 to secure your chance!

Why Join Leben Life Sciences?

• Opportunity to work in an EU-GMP approved global standard facility.
• Be part of a reputed company with over 40 years of pharmaceutical expertise.
• Exposure to regulated international markets.
• Career growth and learning opportunities in a quality-focused organization.
• Contribute to advancing safe and effective medicines worldwide.

Frequently Asked Questions (FAQs)

Q1: What qualifications are required for this role?
Candidates must hold an M.Sc, B.Pharm, or M.Pharm degree with specialization in Chemistry or Pharmaceutical Sciences.

Q2: How much experience is needed?
Applicants should have 2–4 years of Quality Control experience, particularly with HPLC and GLP practices.

Q3: What skills are essential for this position?
Hands-on experience with HPLC, knowledge of GLP/cGMP compliance, and strong documentation skills.

Q4: Where is the job located?
The role is based at Akola, Maharashtra, in LLS’s EU-GMP certified plant.

Q5: How can I apply?
Interested candidates can send their CV to career@lebenlifesciences.com or call the provided contact number.

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