Leben Life Sciences Hiring – Quality Control Officer (HPLC & GLP)

Leben Life Sciences Hiring – Quality Control Officer (HPLC & GLP) | B.Pharm / M.Pharm / M.Sc. | Akola, Maharashtra

Leben Life Sciences Pvt. Ltd. (LLS), a well-established pharmaceutical formulation company with over four decades of industry presence, is expanding its Quality Control team at its EU-GMP approved, global standard OSD and semi-solids manufacturing facility in Akola, Maharashtra. The company is currently hiring Quality Control Officers for HPLC and GLP sections. These roles are ideal for professionals with 1–4 years of relevant pharmaceutical industry experience who are looking to grow their careers in analytical testing, GMP compliance, and regulatory-driven quality systems.

This recruitment drive offers excellent opportunities for B.Pharm, M.Pharm, and M.Sc. graduates to work in a regulatory-compliant manufacturing environment aligned with international guidelines such as IP, BP, USP, and Ph. Eur. If you have hands-on experience in HPLC analysis, calibration, laboratory documentation, and GLP practices within an OSD background, this could be the right step forward in your pharma quality control career.

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Company Overview – Leben Life Sciences Pvt. Ltd.

Leben Life Sciences is a reputed pharmaceutical formulation company known for its commitment to responsible healthcare and high manufacturing standards. With more than 40 years of experience in the pharma industry, the organization has built strong capabilities in oral solid dosage (OSD) and semi-solids manufacturing.

The Akola facility operates under EU-GMP approved global standards, reflecting the company’s strong focus on regulatory compliance, quality assurance, and international market requirements. The company caters to domestic and global markets, ensuring that products meet stringent quality benchmarks through robust analytical testing, validation practices, and documentation systems.

Working at Leben Life Sciences means being part of a structured pharmaceutical manufacturing ecosystem where quality control, data integrity, GMP compliance, and regulatory standards are taken seriously. The organization encourages disciplined laboratory practices, calibration control, instrument qualification, and scientific accuracy in all analytical operations.

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Job Openings in Quality Control Department

Leben Life Sciences is hiring for the following positions at its Akola (Maharashtra) manufacturing unit:

1. Officer – HPLC (Quality Control)

Experience Required: 1–4 Years (OSD Background Preferred)
Qualification: B.Pharm / M.Pharm / M.Sc. (Relevant Life Sciences)
Location: Akola, Maharashtra

2. Officer – GLP (Quality Control)

Experience Required: 1–2 Years
Qualification: B.Pharm / M.Pharm / M.Sc. (Relevant Life Sciences)
Location: Akola, Maharashtra

Candidates must have hands-on exposure to pharmaceutical formulation laboratories and a clear understanding of Good Laboratory Practices and regulatory expectations.

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Job Role & Responsibilities

Officer – HPLC (Quality Control)

The selected candidate will be responsible for analytical testing and instrument management within the QC laboratory. Key responsibilities include:

• Analysis of Raw Materials (RM), In-Process (IP), Finished Goods (FG), and Stability samples using HPLC.
• Performing and documenting HPLC calibration activities as per SOP and schedule.
• Ensuring compliance with pharmacopeial standards such as IP, BP, USP, and Ph. Eur.
• Maintaining data integrity and accurate documentation in line with cGMP requirements.
• Troubleshooting analytical issues and ensuring timely reporting of deviations.
• Supporting regulatory audits by maintaining proper analytical records and logbooks.

This role requires strong analytical skills, accuracy in documentation, and familiarity with chromatographic techniques used in pharmaceutical quality control laboratories.

Officer – GLP (Quality Control)

The GLP Officer will focus on laboratory compliance, calibration, and chemical management activities. Core responsibilities include:

• Performing daily and monthly calibration of pH meters, balances, and other sophisticated laboratory instruments.
• Conducting water testing and preparing volumetric solutions, reagents, and indicators.
• Managing calibration activities for all QC instruments.
• Overseeing chemical inventory and glassware management.
• Ensuring strict adherence to Good Laboratory Practices (GLP).
• Handling Progen-related documentation and system activities.

This position plays a critical role in maintaining laboratory readiness, audit preparedness, and compliance with pharmaceutical regulatory frameworks.

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Eligibility / Qualifications

Candidates applying for these positions must meet the following educational and professional criteria:

Educational Qualification (Relevant Courses):
B.Pharm, M.Pharm, M.Sc. (Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, Organic Chemistry, Biotechnology, Microbiology, Life Sciences)

Experience Requirements:

• 1–4 years of experience in pharmaceutical Quality Control.
• Experience in OSD formulation manufacturing is preferred.
• Strong knowledge of HPLC systems, calibration procedures, and GLP practices.
• Familiarity with pharmacopeial testing methods (IP, BP, USP, Ph. Eur.).
• Exposure to GMP documentation and regulatory inspection readiness.

Candidates must demonstrate attention to detail, compliance mindset, and ability to work in a regulated pharmaceutical manufacturing environment.

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Location & Work Environment

Work Location: Akola, Maharashtra
Facility Type: EU-GMP Approved OSD & Semi-Solids Manufacturing Unit

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Application Process

Interested candidates can apply through the following methods:

📧 Email your updated CV to: career@lebenlifesciences.com
📞 Contact Number: 7498035480
🌐 Company Website: www.lebenlifesciences.com

Ensure your resume clearly highlights:

• Experience in HPLC analysis or GLP activities
• OSD formulation exposure (if applicable)
• Instrument calibration expertise
• Knowledge of pharmacopeial standards

Shortlisted candidates will be contacted for further selection rounds.

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Frequently Asked Questions (FAQs)

1. Who can apply for the Quality Control Officer role at Leben Life Sciences?

Candidates with B.Pharm, M.Pharm, or M.Sc. in relevant life science disciplines and 1–4 years of QC experience in pharmaceutical formulation can apply.

2. Is OSD experience mandatory?

OSD formulation experience is preferred, especially for the HPLC Officer role, but candidates with strong QC analytical experience may also be considered.

3. What instruments should candidates be familiar with?

For HPLC roles, hands-on experience with chromatographic systems is essential. For GLP roles, knowledge of calibration of pH meters, balances, and other QC instruments is required.

4. What regulatory standards should candidates know?

Understanding of IP, BP, USP, and Ph. Eur. standards along with GMP and GLP compliance is important.

5. Where is the job location?

The position is based at the Akola, Maharashtra manufacturing facility.

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Vertical Summary Table

Company	Leben Life Sciences Pvt. Ltd.
Vacancies	Officer – HPLC (Quality Control), Officer – GLP (Quality Control)
Required Education	B.Pharm, M.Pharm, M.Sc. (Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, Life Sciences, Biotechnology, Microbiology)
Experience	1–4 Years (HPLC: 1–4 yrs; GLP: 1–2 yrs; OSD background preferred)

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