Aneta Pharmaceutical Pvt. Ltd. has announced exciting career opportunities for experienced professionals at its OSD (Oral Solid Dosage) Formulation Facility located in Ahmedabad, Gujarat. The company is hiring for Engineering, Quality Control, and Formulation Research & Development (R&D) departments. Candidates with relevant pharmaceutical manufacturing experience are encouraged to apply.

If you are looking for a career in a WHO-GMP-approved pharmaceutical company, this is a great opportunity to join a fast-growing organization.

Job Overview

Particulars Details

Company Name

Aneta Pharmaceutical Pvt. Ltd.

Industry

Pharmaceutical

Job Type

Full-Time

Facility

OSD Formulation Manufacturing

Location

Ahmedabad, Gujarat

Experience Required

2–5 Years

Employment Type

Permanent

Application Mode

Email / WhatsApp / Walk-in

Available Positions

1. Engineering Department

Position: Technician

Area: Maintenance – Electrician

Qualification: ITI

Vacancies: 1

Responsibilities

Preventive and breakdown maintenance of electrical equipment.

Troubleshooting electrical systems.

Ensuring uninterrupted production operations.

Maintaining electrical safety standards.

2. Quality Control Department

Position: Officer / Senior Officer

Qualification: M.Sc. / B.Sc.

Vacancies: 1

Required Experience

Candidates should have hands-on experience with:

HPLC

UV Spectrophotometer

Dissolution

DT (Disintegration Test)

Friability Tester

In-Process Testing

Finished Product Analysis

Responsibilities

Raw material testing

Finished product analysis

Stability testing

Documentation as per GMP & GLP

Instrument calibration

Laboratory compliance

3. Formulation Research & Development (OSD)

Position

RA / Sr. RA

Qualification

M.Pharm

Ph.D.

Experience

2–5 Years

Key Responsibilities

Product development

Process development

Pilot-scale manufacturing

Technology transfer

Technical documentation

Regulatory compliance

Formulation optimization

Process validation support

4. Formulation R&D – Machine Operator

Position

Operator

Qualification

10th Pass

ITI

Experience Required

Candidates should have experience in F&D machine handling such as:

Granulation

Compression

Coating Machines

Eligibility Criteria

Applicants should have:

2–5 years of relevant pharmaceutical experience.

Experience in OSD manufacturing or laboratory operations.

Strong knowledge of GMP, GLP, and pharmaceutical documentation.

Good communication and teamwork skills.

Job Location

Ahmedabad, Gujarat

How to Apply

Interested candidates can apply through any of the following methods:

Email: hr@anetapharma.com

WhatsApp: +91 7575809274

Walk-in Timing: Between 12:00 PM and 2:00 PM (excluding Tuesday)

Company Website: https://anetapharma.com/

About Aneta Pharmaceutical Pvt. Ltd.

Aneta Pharmaceutical Pvt. Ltd. was established in 2023 and specializes in the manufacturing of pharmaceutical medicines. The company operates a WHO-GMP-approved OSD manufacturing facility and follows GLP-compliant quality systems. It focuses on delivering high-quality pharmaceutical products while maintaining strict regulatory standards and continuous innovation.

Why Join Aneta Pharmaceutical?

WHO-GMP approved manufacturing facility

Modern OSD formulation plant

Career growth opportunities

Exposure to Research & Development

Professional work environment

Quality-driven organization

Selection Process

Application Screening

HR Shortlisting

Technical Interview

Final HR Discussion

Offer Letter

Required Documents

Updated Resume

Educational Certificates

Experience Certificates

Latest Salary Slip (if applicable)

Government ID Proof

Passport-size Photograph

Technical FAQs

1. What analytical instruments should a Quality Control candidate be proficient in?

Candidates should have practical experience with HPLC, UV Spectrophotometer, Dissolution Apparatus, Disintegration Tester (DT), Friability Tester, and in-process testing instruments commonly used in pharmaceutical quality control laboratories.

2. What is the role of a Research Associate (RA) in OSD Formulation R&D?

An RA develops and optimizes oral solid dosage formulations, conducts pilot-scale trials, prepares technical documentation, supports technology transfer, and ensures compliance with regulatory guidelines during product development.

3. What GMP and GLP knowledge is expected for these positions?

Candidates should understand Good Manufacturing Practices (GMP) for production and Good Laboratory Practices (GLP) for laboratory operations, including documentation, SOP adherence, data integrity, equipment calibration, and quality compliance.

4. What skills are required for the Formulation R&D Machine Operator role?

Operators should be experienced in handling granulation, compression, and coating machines, performing equipment setup, monitoring process parameters, troubleshooting basic issues, and maintaining proper batch documentation.

5. Why is HPLC important in pharmaceutical Quality Control?

High-Performance Liquid Chromatography (HPLC) is used to accurately identify and quantify active pharmaceutical ingredients (APIs), impurities, degradation products, and finished products, ensuring medicines meet quality and regulatory specifications.