Eben Life Sciences Hiring QC Officers

MSc BPharm QC Officer Jobs in Akola – Eben Life Sciences

Eben Life Sciences hiring QC Officers in Akola. MSc, BPharm, MPharm eligible. 1–4 yrs experience. Immediate joiners preferred.

Eben Life Sciences has announced a mega hiring drive for its Quality Control department at the Akola manufacturing facility in Maharashtra. This opportunity is aimed at skilled QC professionals with hands-on exposure to GLP, HPLC, and stability studies in a regulated pharmaceutical formulation environment. Candidates with 1 to 4 years of relevant experience who are ready to join immediately will be given preference.

With increasing regulatory scrutiny and growing demand for quality-driven pharmaceutical manufacturing, quality control roles continue to be among the most stable and high-demand careers in the pharma sector. This opening at Eben Life Sciences offers the chance to work in a globally approved manufacturing facility while contributing directly to product quality, regulatory compliance, and patient safety.

Company Overview

Eben Life Sciences, also known as Leben Life Sciences Pvt. Ltd., is an established pharmaceutical formulation company with a strong presence in domestic and international markets. The company operates a global-standard manufacturing facility at Akola, Maharashtra, approved by multiple international regulatory authorities.

Leben Life Sciences is known for its commitment to quality, compliance, and continuous improvement across its manufacturing and quality operations. The organization follows stringent GMP and GLP systems aligned with global pharmacopoeial and regulatory expectations. Working at Eben Life Sciences provides professionals with exposure to regulated quality systems, advanced analytical practices, and long-term career growth in pharmaceutical quality control.

Job Role & Responsibilities

Quality Control Officer – GLP / HPLC / Stability

The Quality Control Officer will be responsible for routine, stability, and compliance-related analytical activities within the QC laboratory.

Stability Responsibilities

• Handling and management of stability samples
• Stability chamber monitoring and data review
• Preparation of stability protocols, reports, and trackers
• Analysis of raw materials, in-process samples, finished products, hold-time, and stability samples using HPLC and UV techniques

HPLC Responsibilities

• Operation and calibration of HPLC instruments
• Assay, dissolution, related substances, UOC, and swab/rinse analysis
• Analysis of RM, IP, and finished products
• Working knowledge of IP, BP, USP, and Ph.Eur pharmacopoeias

GLP Responsibilities

• Calibration of pH meters, balances, and QC instruments
• Water analysis as per pharmacopeial standards
• Reagent and solution preparation
• GLP compliance, chemical handling, and glassware management

This role is ideal for candidates seeking pharmaceutical quality control jobs with strong exposure to analytical compliance and stability studies.

Eligibility / Qualifications

Educational Qualifications

• M.Sc. (Chemistry, Pharmaceutical Chemistry, Analytical Chemistry)
• B.Pharm
• M.Pharm

(Relevant courses: BPharmacy, MPharmacy – Pharmaceutical Analysis, Pharmaceutics, Quality Assurance, MSc Chemistry, MSc Analytical Chemistry)

Experience Requirements

• 1 to 4 years of experience in pharmaceutical quality control
• Practical exposure to GLP, HPLC, and stability activities

Required Skills

• Strong understanding of GMP and GLP systems
• Hands-on experience with HPLC and UV analysis
• Stability study management and documentation
• Knowledge of pharmacopeial standards
• Attention to detail and data integrity awareness

These competencies align with high-CPC pharma QC jobs and analytical quality roles.

Location & Salary

Job Location: Akola, Maharashtra

Salary: Salary will be offered as per industry standards and will depend on qualification, experience, and interview performance. Eben Life Sciences offers stable compensation, compliance-focused work culture, and long-term career growth.

Application Process

Interested and eligible candidates can apply by sending their updated CV to the official email ID.

Apply Now: career@lebenlifesciences.com

Candidates are advised to mention “QC Officer – GLP/HPLC/Stability” in the email subject line for faster shortlisting.

Immediate joiners will be given preference due to operational requirements.

Why Join Eben Life Sciences

• Global-standard manufacturing facility with regulatory approvals
• Strong quality-driven organizational culture
• Exposure to GLP, HPLC, and stability programs
• Career growth in regulated pharmaceutical quality control
• Direct contribution to safe and effective healthcare products

These roles are well suited for candidates searching for pharma QC jobs in Maharashtra, HPLC analyst roles, stability officer jobs, and pharmaceutical quality control careers.

FAQs

Who can apply for this QC Officer role?

Candidates with M.Sc., B.Pharm, or M.Pharm qualifications and 1–4 years of QC experience can apply.

Is stability experience mandatory?

Yes. Experience in stability studies and chamber management is required for this role.

Are freshers eligible?

No. This position requires prior pharmaceutical QC experience.

Is immediate joining mandatory?

Immediate joiners are preferred, but final selection will depend on business requirements.

Is there any application fee?

No. Eben Life Sciences does not charge any recruitment or application fees.

Summary Table

Company	Eben Life Sciences (Leben Life Sciences Pvt. Ltd.)
Vacancies	Quality Control Officer (GLP / HPLC / Stability)
Required Education	M.Sc., B.Pharm, M.Pharm
Experience	1–4 years