Aneta Pharmaceuticals Recruitment – Engineering & Quality Control Opportunities in Ahmedabad

Aneta Pharmaceuticals Pvt. Ltd., a growing pharmaceutical company with a WHO-GMP-approved manufacturing facility, has announced multiple openings for experienced professionals at its OSD (Oral Solid Dosage) formulation facility in Ahmedabad, Gujarat. The company is seeking skilled candidates for Engineering and Quality Control departments with relevant pharmaceutical industry experience.

This recruitment drive offers excellent opportunities for professionals looking to advance their careers in pharmaceutical manufacturing, quality assurance, and engineering operations.

Company Overview

Aneta Pharmaceuticals was established in 2023 and specializes in the manufacturing of pharmaceutical products. The company emphasizes quality, innovation, and compliance with global pharmaceutical standards. Its production facility follows WHO-GMP guidelines and GLP-compliant quality control practices.

Available Positions

1. Engineering Department

Officer – Electrical / QMS / Instrumentation

Vacancies: 2

Experience: 2–5 Years

Qualification: B.E. / M.E. / Diploma

Department: Engineering

Technician – Maintenance Electrician

Vacancies: 1

Experience: 2–5 Years

Qualification: ITI

Department: Engineering

2. Quality Control Department

Officer / Senior Officer – Analyst (DISSO/UV/RM/PM)

Vacancies: 3

Experience: 2–5 Years

Qualification: M.Sc. / B.Sc.

Department: Quality Control

Job Location

Ahmedabad, Gujarat

Employment Type: Full-Time

Application Process

Interested candidates can submit their updated CV through the following channels:

Email: hr@anetapharma.com

WhatsApp: +91 7575809274

Walk-In Timing: Between 12:00 PM and 2:00 PM

Company Website: https://anetapharma.com

Why Join Aneta Pharmaceuticals?

Opportunity to work in a WHO-GMP-approved facility.

Exposure to modern pharmaceutical manufacturing processes.

Growth-oriented work environment.

Competitive career opportunities in Engineering and Quality Control.

Focus on quality, compliance, and innovation.

Technical FAQs

1. What is DISSO analysis in pharmaceutical Quality Control?

Dissolution (DISSO) analysis is a laboratory test used to determine the rate and extent at which an active pharmaceutical ingredient (API) is released from a dosage form. It is a critical quality parameter for tablets and capsules.

2. What is the role of UV spectroscopy in Quality Control?

UV-Visible Spectroscopy is used for qualitative and quantitative analysis of pharmaceutical products. It helps determine drug concentration, assay values, and impurity profiles according to validated analytical methods.

3. What responsibilities does an Instrumentation Officer handle in a pharmaceutical plant?

An Instrumentation Officer manages calibration, preventive maintenance, troubleshooting, and compliance of instruments such as pressure gauges, temperature sensors, transmitters, and PLC/SCADA systems.

4. Why is electrical maintenance important in pharmaceutical manufacturing?

Electrical maintenance ensures uninterrupted operation of production equipment, HVAC systems, purified water systems, and utility equipment while maintaining GMP compliance and operational safety.

5. What is the significance of GLP in Quality Control laboratories?

Good Laboratory Practices (GLP) ensure the accuracy, reliability, consistency, and traceability of laboratory testing activities. GLP compliance helps maintain data integrity and regulatory acceptance.

Conclusion

Aneta Pharmaceuticals is offering promising career opportunities for professionals with 2–5 years of experience in Engineering and Quality Control functions. Candidates possessing expertise in electrical systems, instrumentation, maintenance, dissolution testing, and analytical laboratory operations are encouraged to apply. With its commitment to quality and regulatory excellence, Aneta Pharmaceuticals provides a strong platform for long-term professional growth in the pharmaceutical sector.