Zeon Lifesciences Limited, a leading nutraceutical and pharmaceutical manufacturing company, has announced exciting career opportunities at its USFDA-approved manufacturing facility in Paonta Sahib, Sirmaur, Himachal Pradesh. The company is seeking talented professionals for Formulation & Development (F&D), Production, Quality Control (QC), Project Engineering, and Manufacturing Operations departments.

This recruitment drive offers excellent opportunities for candidates from B.Pharm, M.Pharm, B.Sc, M.Sc, ITI, 10th, and 12th backgrounds who are looking to build a rewarding career in the pharmaceutical and nutraceutical industry.

Company Details

• Company Name: Zeon Lifesciences Limited
• Location: Paonta Sahib, Sirmaur, Himachal Pradesh
• Industry: Pharmaceutical & Nutraceutical Manufacturing
• Facility: USFDA-Approved Manufacturing Plant

Available Positions

1. AM / DM – Tablet, Capsule & Liquid Formulation Development

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Food)
Experience: 5–9 Years

2. Executive / Sr. Executive – Liquid Project Development Scientist

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Food)
Experience: 3–6 Years

3. Officer / Executive – Dry Powder Formulation & Development

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Food)
Experience: 1–3 Years

4. Manufacturing Officer – Production (Liquid Area)

Qualification: B.Pharm / B.Sc
Experience: 2–5 Years

5. Manufacturing Operator – Production (Liquid Area)

Qualification: ITI / 10th / 12th
Experience: 2–8 Years

6. Officer – Quality Control (HPLC Section)

Qualification: B.Pharm / B.Sc / M.Sc
Experience: 2–5 Years

7. Manufacturing Officer – Production (Powder Area)

Qualification: B.Pharm / B.Sc
Experience: 2–5 Years

Key Benefits

• Growth-oriented work environment
• USFDA-approved manufacturing facility
• Competitive salary package
• Career development opportunities
• Exposure to advanced pharmaceutical technologies

Application Process

Interested candidates can send their updated CV to the company’s HR department.

Email: hr4@zeon.co.in
WhatsApp: 8894729624

Technical FAQs

1. What is Formulation & Development (F&D) in the pharmaceutical industry?

Formulation & Development involves designing and optimizing pharmaceutical products such as tablets, capsules, powders, and liquid formulations while ensuring quality, stability, and regulatory compliance.

2. What is the role of HPLC in Quality Control?

HPLC (High Performance Liquid Chromatography) is used for identification, assay, impurity profiling, and quality testing of pharmaceutical products to ensure product safety and effectiveness.

3. What are the key GMP requirements for production personnel?

Production personnel must follow Good Manufacturing Practices (GMP), including documentation, hygiene procedures, equipment cleaning, process validation, and deviation management.

4. What skills are required for Liquid Manufacturing Operations?

Candidates should have knowledge of batch manufacturing processes, mixing systems, CIP/SIP operations, equipment handling, process monitoring, and GMP documentation.

5. Why is experience in a USFDA-approved facility valuable?

Working in a USFDA-approved facility provides exposure to global regulatory standards, data integrity requirements, quality systems, validation processes, and international audit practices.