Leben Life Sciences Hiring QA Officers & Sr. Officers

QA Officer & Sr. Officer | B Pharm/M.Pharm | Akola

Leben Life Sciences hiring QA Officers & Sr. Officers at Akola. B Pharm, M.Pharm, MSc candidates with 2–4 yrs experience can apply.

---

Leben Life Sciences Pvt. Ltd. (LLS), a trusted name in pharmaceutical formulations for over 40 years, is expanding its Quality Assurance (QA) team at its EU-GMP approved OSD and Semi-Solid manufacturing facility in Akola, Maharashtra. This is a unique opportunity for candidates with a strong background in B Pharm, M.Pharm, or MSc to join a global-standard production environment and contribute to high-quality pharmaceutical products.

---

Company Overview

Leben Life Sciences Pvt. Ltd. (LLS) has been a cornerstone of pharmaceutical innovation and manufacturing for over four decades. With a commitment to responsible healthcare and quality excellence, LLS operates EU-GMP certified facilities, delivering safe, effective, and reliable pharmaceutical formulations worldwide.

Joining LLS offers exposure to cutting-edge OSD and semi-solid formulation processes, cross-functional collaboration, and career growth within a globally recognized organization.

---

Job Role & Responsibilities

Sr. Officer – Documentation

• Ensure accurate and timely preparation, review, and maintenance of QA documentation.

• Implement and maintain cGMP-compliant documentation systems.

• Support quality management systems (QMS) activities, including SOPs, protocols, and batch records.

• Collaborate with cross-functional teams to ensure regulatory and compliance standards are met.

Officer – AQA (Analytical Quality Assurance)

• Conduct routine quality audits and checks in line with EU-GMP standards.

• Monitor and ensure compliance with quality policies and procedures.

• Participate in CAPA investigations, deviations, and change control documentation.

• Provide support in regulatory inspections and ensure all QA processes are documented accurately.

Both positions require a keen eye for detail, organizational skills, and the ability to maintain high standards of quality in a fast-paced environment.

---

Eligibility / Qualifications

• Educational Qualification: B Pharm, M.Pharm, MSc in relevant disciplines.

• Experience:

  • Sr. Officer (Documentation): 2–4 years

  • Officer (AQA): 2+ years

• Skills & Requirements:

  • Understanding of GMP and EU-GMP compliance standards.

  • Strong documentation, communication, and analytical skills.

  • Male candidates preferred due to facility requirements.

---

Location & Salary

Work Location: Akola, Maharashtra – EU-GMP Approved OSD & Semi-Solid Manufacturing Facility
alary: As per industry standards and experience.

---

Application Process

Interested candidates can send their updated CV to:

career@lebenlifesciences.com
Contact: 7498035480

Apply today to join a globally recognized QA team and advance your pharmaceutical career at Leben Life Sciences!

---

Why Join Leben Life Sciences

• Work in an EU-GMP approved facility with global standards.

• Gain exposure to OSD and semi-solid pharmaceutical manufacturing.

• Opportunity to work in Quality Assurance and Analytical QA with career growth potential.

• Be part of a company with over four decades of trusted healthcare contributions.

---

FAQs – QA Careers at Leben Life Sciences

Q1. Can freshers apply for these QA positions?
No, candidates must have 2+ years of relevant experience in QA or documentation.

Q2. Are both male and female candidates eligible?
Currently, male candidates are preferred due to operational requirements at the facility.

Q3. What is the application deadline?
Applications are accepted on a rolling basis; early applications are encouraged.

Q4. What documents should be submitted?
Submit your updated CV, academic certificates, and experience letters to the HR email.

Q5. Does Leben Life Sciences offer growth opportunities?
Yes, employees are encouraged to grow within QA, Regulatory Affairs, and other pharma departments.

---

Summary Table