Pharma Job Alert: Viatris Walk-In Drive for Quality Control Professionals in Goa & Nashik

The pharmaceutical industry continues to offer excellent career opportunities for skilled professionals who possess strong analytical expertise and regulatory knowledge. If you have experience in pharmaceutical quality control and are looking to work with a globally recognized healthcare organization, an exciting opportunity is now available.

Viatris, one of the world’s leading healthcare companies, has announced a major walk-in recruitment drive for Quality Control professionals for its Oral Solid Dosage (OSD) manufacturing facility located in Nashik, Maharashtra. The company is inviting qualified candidates with relevant QC experience to participate in the upcoming hiring event scheduled in Goa.

This recruitment campaign offers a valuable opportunity for candidates seeking career growth, advanced laboratory exposure, international regulatory experience, and long-term professional development within a globally respected pharmaceutical organization.

About Viatris

Viatris was formed through the combination of Mylan and Upjohn and has grown into a global healthcare company committed to providing access to high-quality medicines worldwide.

The organization operates manufacturing facilities, research centers, and commercial operations across numerous countries and serves millions of patients globally. Viatris is known for maintaining high-quality manufacturing standards and complying with international regulatory requirements including:

USFDA
MHRA
EMA
TGA
WHO-GMP

The company’s facilities employ modern technology, robust quality systems, and advanced analytical laboratories that provide excellent learning opportunities for pharmaceutical professionals.

Walk-In Recruitment Overview

Particulars	Details
Company	Viatris (Mylan Laboratories Limited)
Department	Quality Control
Designation	QC Analyst / Senior Analyst
Manufacturing Segment	Oral Solid Dosage (OSD)
Plant Location	Nashik, Maharashtra
Qualification	M.Sc Chemistry, B.Pharm, M.Pharm
Experience	2–4 Years
Interview Type	Walk-In Interview
Interview Date	21 June 2026
Interview Time	10:00 AM to 5:00 PM
Interview Venue	Kesarval The Fern Goa, Cortalim, Goa
Application Mode	Walk-In & Email Submission

Why Quality Control Professionals Are in High Demand

Quality Control plays a critical role in ensuring the safety, efficacy, and quality of pharmaceutical products before they reach patients.

With increasing global regulatory expectations, pharmaceutical companies require highly trained analysts who can:

Conduct analytical testing
Ensure data integrity
Investigate laboratory deviations
Support regulatory inspections
Maintain compliance with GMP standards
Handle sophisticated analytical instruments

As pharmaceutical exports continue to increase, the demand for experienced QC professionals remains strong across India’s manufacturing sector.

Available Positions

The company is currently recruiting for:

Quality Control Analyst

Professionals in this role will perform routine analytical testing of raw materials, in-process samples, stability samples, and finished products.

Key Responsibilities

Sample analysis using HPLC and GC
Dissolution testing
UV spectroscopy analysis
IR analysis
Stability sample testing
Documentation review
Data recording and reporting
GMP compliance activities

Senior Quality Control Analyst

Candidates with stronger technical expertise and investigation experience may be considered for senior positions.

Additional Responsibilities

OOS investigations
OOT investigations
Laboratory deviation handling
Root cause analysis
CAPA implementation
Method troubleshooting
Team guidance and mentoring
Audit preparation support

Technical Skills Required

The company is specifically looking for professionals who possess hands-on laboratory experience.

1. HPLC Operation and Troubleshooting

Candidates should have practical experience with:

Waters HPLC
Agilent HPLC
Shimadzu HPLC
Empower Software
Chromatographic analysis
System suitability testing
Instrument troubleshooting

Experience with method execution and routine maintenance will be highly valued.

2. Gas Chromatography (GC)

Applicants should be capable of:

Performing GC analysis
Instrument calibration
Data interpretation
Troubleshooting analytical issues
Following validated analytical procedures

3. Dissolution Testing

Knowledge of dissolution apparatus operation is essential.

Candidates should understand:

Dissolution profile evaluation
Sampling procedures
Regulatory requirements
Data analysis
Instrument qualification concepts

4. UV and IR Spectroscopy

Practical exposure to:

UV-Visible Spectrophotometers
FTIR instruments
Sample preparation
Identification testing
Routine laboratory analysis

will provide an added advantage.

Laboratory Information Management Systems (LIMS)

Modern pharmaceutical laboratories rely heavily on digital systems.

Candidates with experience in:

Sample login
Test assignment
Result entry
Electronic documentation
Data tracking
Audit trail management

through Laboratory Information Management Systems (LIMS) will be preferred.

Computer System Validation (CSV) Knowledge

Regulatory agencies increasingly focus on electronic data integrity.

Therefore, Viatris is seeking candidates who understand:

Computer System Validation
Electronic records
Electronic signatures
Audit trails
Data integrity principles
21 CFR Part 11 compliance

Such expertise significantly enhances employability within regulated pharmaceutical environments.

Experience in OOS, OOT and Deviations

One of the most important requirements for this hiring drive is investigation experience.

Out of Specification (OOS)

Candidates should understand:

OOS initiation
Laboratory investigations
Phase I investigations
Phase II investigations
Root cause determination
Corrective actions

Out of Trend (OOT)

Experience in:

Trend monitoring
Data analysis
Statistical evaluation
Investigation procedures

will be highly beneficial.

Deviation Handling

Quality systems require proper deviation management.

Candidates should possess exposure to:

Incident reporting
Deviation investigation
CAPA implementation
Effectiveness checks
Quality documentation

Educational Qualifications Required

Candidates must possess any of the following qualifications:

M.Sc Chemistry

Applicants with specialization in:

Organic Chemistry
Analytical Chemistry
Pharmaceutical Chemistry

are eligible.

B.Pharm

Bachelor of Pharmacy graduates with relevant industrial QC experience may apply.

M.Pharm

Candidates with postgraduate pharmacy qualifications and analytical laboratory experience are encouraged to participate.

Experience Criteria

The company has specified:

Required Experience

Minimum: 2 Years
Maximum: 4 Years

Industry Background

Candidates should have worked in:

Pharmaceutical manufacturing companies
Regulated manufacturing facilities
GMP environments

Mandatory Requirement

Experience in Oral Solid Dosage (OSD) manufacturing is highly preferred.

This includes:

Tablets
Capsules
Coated tablets
Extended-release products

Candidates without OSD experience may face challenges during the screening process.

Benefits of Working at Viatris

Global Exposure

Employees gain experience working under international regulatory standards.

This exposure strengthens professional profiles and opens future opportunities across multinational pharmaceutical organizations.

Advanced Analytical Laboratories

The Nashik manufacturing facility offers access to:

Modern HPLC systems
Advanced GC equipment
Automated analytical platforms
Electronic laboratory systems
Data integrity-compliant infrastructure

Career Growth Opportunities

Employees can benefit from:

Internal promotions
Skill enhancement programs
Leadership development
Technical training
Cross-functional exposure

Stable Corporate Environment

Viatris provides a structured corporate culture focused on:

Employee development
Continuous learning
Compliance excellence
Innovation
Professional growth

Walk-In Interview Venue Details

Interview Date

21 June 2026

Interview Timing

10:00 AM to 5:00 PM

Venue

Kesarval The Fern Goa

Verna Edapally–Panvel Highway

Cortalim, Goa

Candidates are advised to arrive early to complete registration formalities and avoid waiting times.

Documents to Carry

Applicants should bring:

Updated Resume
Passport-size photographs
Educational certificates
Experience certificates
Latest increment letter
Current CTC structure
Last three salary slips
Government ID proof
PAN Card copy

Carrying complete documentation can significantly speed up the interview process.

Unable to Attend? Apply Through Email

Candidates who cannot attend the walk-in drive may submit their resumes directly to the HR team.

Official Application Email

Abhinay.kharde@viatris.com

Suggested Email Subject

Application for QC OSD – Nashik Plant – Your Name – Experience

Example:

Application for QC OSD – Nashik Plant – Rahul Sharma – 3 Years Experience

Tips to Improve Your Selection Chances

Before attending the interview:

Update Your Resume

Clearly mention:

HPLC platforms used
GC experience
Dissolution testing expertise
OOS investigations
OOT investigations
LIMS experience
CSV exposure

Prepare Technical Questions

Review:

GMP principles
Data Integrity
OOS procedures
HPLC troubleshooting
Dissolution testing
Chromatography fundamentals

Highlight Regulatory Exposure

Interviewers often prefer candidates who have worked during:

USFDA audits
MHRA audits
WHO inspections
Internal quality audits

Final Thoughts

The Viatris Walk-In Recruitment Drive 2026 presents an outstanding opportunity for Quality Control professionals looking to advance their careers within a globally recognized pharmaceutical company. Candidates with strong analytical expertise, OSD manufacturing experience, and knowledge of regulatory compliance systems stand a strong chance of securing a rewarding role.

If you meet the eligibility requirements, make sure to attend the walk-in interview on 21 June 2026 or send your updated CV to the HR team. Opportunities with multinational pharmaceutical organizations like Viatris can significantly accelerate professional growth while providing exposure to international quality standards and advanced analytical technologies.

Don’t miss this excellent opportunity to become part of a company committed to improving global healthcare and delivering quality medicines to patients worldwide.

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