RV Lifesciences Walk-In Interview Drive| Multiple Openings in QC, QA, Manufacturing, Packing, Warehouse & Engineering

RV Lifesciences Ltd. (RVLL), a Singapore-based multinational pharmaceutical company, has announced an urgent walk-in interview drive for its OSD manufacturing facility located at Waluj, Chhatrapati Sambhajinagar, Maharashtra. The company operates across eight countries and is expanding its pharmaceutical manufacturing operations, creating excellent career opportunities for experienced professionals and freshers.

This recruitment drive offers positions in Quality Control, Quality Assurance, Engineering, Warehouse, Packing, Manufacturing, and PPC departments.

About RV Lifesciences Ltd

RV Lifesciences Ltd. is a globally recognized pharmaceutical company with state-of-the-art OSD (Oral Solid Dosage) manufacturing facilities in Myanmar, Vietnam, and India. The organization follows international quality standards and holds certifications including:

ISO 9001

WHO-GMP

Russia GMP

EU GMP

The company is known for its commitment to quality, compliance, innovation, and global pharmaceutical excellence.

Walk-In Interview Details

Particulars Details

Company Name

RV Lifesciences Ltd.

Interview Type

Walk-In Interview Drive

Interview Dates

19th & 20th June 2026 (Friday & Saturday)

Interview Time

09:00 AM to 04:00 PM

Job Location

Waluj, Chhatrapati Sambhajinagar, Maharashtra

Industry

Pharmaceutical Manufacturing (OSD)

Venue

RV Lifesciences Ltd.

Plot No. H-19, MIDC Waluj,

Chhatrapati Sambhajinagar – 431133,

Maharashtra, India

Department Wise Vacancy Details

Quality Control (QC)

HPLC Analyst

Openings: 10

Qualification: B.Sc / M.Sc

Experience: 2–5 Years

Reviewer

Openings: 5

Qualification: B.Pharm / M.Pharm

Experience: 5–10 Years

Dissolution Specialist

Openings: 4

Qualification: B.Pharm / M.Sc

Experience: 2–5 Years

Quality Assurance (QA)

IPQA

Openings: 5

Qualification: B.Pharm

Experience: 2–3 Years

QMS

Openings: 4

Qualification: B.Pharm

Experience: 3–6 Years

Analytical QA

Openings: 3

Qualification: B.Pharm

Experience: 3–4 Years

P&D

Openings: 1

Qualification: B.Pharm

Experience: 3–4 Years

Engineering Department

Water System Operator

Openings: 1

Qualification: ITI / D.Pharm / B.Sc

Experience: 1–2 Years

Electrician

Openings: 2

Qualification: ITI / Diploma (Electrical)

Experience: 2–3 Years

Fitter

Openings: 2

Qualification: ITI / Diploma (Mechanical)

Experience: 2–3 Years

Apprentice

Openings: 3

Qualification: ITI / B.Sc

Experience: Fresher

Warehouse Department

Dispensing Operator

Openings: 2

Qualification: 12th / B.Sc

Experience: 2–3 Years

Officer

Openings: 1

Qualification: B.Sc / M.Sc

Experience: 2–3 Years

FG Officer

Openings: 1

Qualification: B.Sc / M.Sc

Experience: 2–3 Years

SPM Dispensing Operator

Openings: 1

Qualification: 12th / B.Sc

Experience: 2–3 Years

SPM Officer

Openings: 1

Qualification: B.Sc / M.Sc

Experience: 2–3 Years

High Reach Operator

Openings: 1

Qualification: 12th / ITI

Experience: 2–4 Years

Packing Department

Blister Machine Operator

Openings: 3

Qualification: 12th / B.Sc

Experience: 2–3 Years

Strip Machine Operator

Openings: 2

Qualification: 12th / B.Sc

Experience: 2–3 Years

Officer

Openings: 4

Qualification: B.Pharm

Experience: 3–5 Years

Executive

Openings: 1

Qualification: B.Pharm

Experience: 5–7 Years

Apprentice

Openings: 2

Qualification: B.Pharm

Experience: Fresher

Manufacturing Department

Granulation Operator

Openings: 4

Qualification: 12th / B.Sc

Experience: 2–3 Years

Compression Operator

Openings: 4

Qualification: 12th / B.Sc

Experience: 2–3 Years

Coating Operator

Openings: 4

Qualification: 12th / B.Sc

Experience: 2–3 Years

Officer

Openings: 4

Qualification: B.Pharm

Experience: 3–5 Years

Executive

Openings: 2

Qualification: B.Pharm

Experience: 5–7 Years

Apprentice

Openings: 6

Qualification: B.Pharm / M.Pharm

Experience: Fresher

PPC Department

Trainee / Apprentice

Openings: 1

Qualification: B.Pharm / B.Sc

Experience: Fresher

Key Responsibilities

Quality Control

HPLC/GC analysis

Sample preparation and calibration

Dissolution testing

OOS/OOT investigation

COA review and approval

Quality Assurance

IPQA activities

Line clearance

BMR review

Deviation handling

CAPA implementation

SOP compliance

Manufacturing

Granulation, Compression and Coating operations

Process monitoring

GMP documentation

BMR compliance

In-process checks

Packing

Blister and Strip packing operations

Packing line supervision

Documentation and GMP compliance

Warehouse

Material dispensing

Inventory management

FG handling and dispatch

Forklift and material handling operations

Engineering

Utility and water system operation

Preventive maintenance

Electrical and mechanical troubleshooting

Documents Required

Candidates should carry:

Updated Resume/CV

Passport Size Photographs (2 Copies)

Educational Certificates (Original & Photocopies)

Experience Certificates

Last 3 Months Salary Slips

Aadhaar Card / PAN Card Copy

Bank Account Details

Latest Increment Letter (If Available)

Appointment Letter (If Available)

Important Note

Candidates with pharmaceutical OSD manufacturing experience will be preferred.

Freshers are eligible to apply for Apprentice and Trainee positions.

Immediate joiners may receive preference during the selection process.

Technical FAQs

1. What is the role of an HPLC Analyst in a pharmaceutical QC laboratory?

An HPLC Analyst performs analysis of raw materials, in-process samples, and finished products using High Performance Liquid Chromatography (HPLC) while ensuring compliance with pharmacopoeial and regulatory standards.

2. What are CAPA activities in Quality Assurance?

CAPA (Corrective and Preventive Action) is a quality management process used to investigate deviations, identify root causes, implement corrective actions, and prevent recurrence.

3. Why is line clearance important in pharmaceutical manufacturing?

Line clearance ensures that equipment and production areas are free from previous product residues, documents, and materials, preventing mix-ups and cross-contamination.

4. What is the purpose of dissolution testing?

Dissolution testing evaluates the rate and extent of drug release from a dosage form, ensuring product quality, consistency, and bioavailability.

5. What are the critical process parameters during tablet compression?

Key parameters include tablet weight, hardness, thickness, friability, compression force, and disintegration time, which directly impact product quality and regulatory compliance.