SunGlow Walk-In QA, Production, QC & Regulatory Affairs

SunGlow Walk-In QA, Production, QC & Regulatory Affairs (1)
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SunGlow Lifescience Walk-In | Pharma Jobs | Tamil Nadu

SunGlow Lifescience hiring for QA, Production, QC & Regulatory Affairs. B.Pharm, M.Pharm, ITI, Diploma eligible in Kanchipuram.

SunGlow Lifescience Private Limited has announced a major walk-in interview drive for experienced pharmaceutical professionals across multiple departments including Quality Assurance, Regulatory Affairs, Production, Packing, QC, ARD, Maintenance, Machine Operations, FRD, and Project Management. Candidates looking for pharma manufacturing jobs, pharmaceutical company vacancies, regulatory affairs careers, quality assurance jobs, production executive openings, and healthcare industry opportunities in Tamil Nadu can attend this latest walk-in recruitment drive.

The hiring drive is scheduled for 10th May 2026 and offers opportunities for candidates with pharmaceutical manufacturing, quality control, engineering, and healthcare industry experience. SunGlow Lifescience is actively hiring skilled professionals to support its growing pharmaceutical operations and manufacturing expansion.

Candidates with B.Pharm, M.Pharm, ITI, Diploma, BE, and engineering qualifications who are searching for high-growth pharmaceutical careers, pharma plant jobs, regulatory affairs positions, and GMP manufacturing opportunities can explore this recruitment drive.

Company Overview

SunGlow Lifescience Private Limited is a pharmaceutical manufacturing company engaged in producing high-quality healthcare and pharmaceutical products for domestic and international markets. The company focuses on pharmaceutical manufacturing excellence, regulatory compliance, quality assurance systems, and advanced healthcare production practices.

The organization operates manufacturing facilities with a strong emphasis on GMP compliance, pharmaceutical quality systems, validation processes, engineering maintenance, and international regulatory standards. SunGlow Lifescience continues to expand its workforce to support increasing pharmaceutical production demands and healthcare market growth.

The company provides career opportunities for pharmaceutical professionals, engineering experts, regulatory affairs specialists, production executives, machine operators, and healthcare manufacturing teams.

Job Role & Responsibilities

Quality Assurance Department

Available Roles

  • IPQA
  • AQA
  • Documentation
  • Validation

Regulatory Affairs Department

Available Roles

  • International Market Executive

Maintenance Department

Available Roles

  • HVAC Executive
  • Electrical C Licence Executive
  • Trainee

Machine Operators Department

Available Roles

  • Tablet Coating Operator
  • Compression Operator
  • Blister Operator
  • Ointment Operator
  • Granulation Operator
  • Trainee Operator

FRD Department

Available Roles

  • Executive

Production & Packing Department

Available Roles

  • Officer
  • Executive

QC & ARD Department

Available Roles

  • Executive

Project Management Department

Available Roles

  • Manager
  • Senior Executive

Key Responsibilities

Selected candidates will be responsible for pharmaceutical manufacturing operations, regulatory compliance, production activities, documentation management, quality assurance systems, and healthcare manufacturing support.

Core Responsibilities

  • Maintain GMP and pharmaceutical quality standards
  • Handle production and packing operations efficiently
  • Support validation and documentation activities
  • Monitor quality assurance and quality control procedures
  • Operate pharmaceutical manufacturing machinery
  • Maintain engineering systems including HVAC and electrical operations
  • Ensure compliance with international regulatory guidelines
  • Support pharmaceutical research and formulation activities
  • Coordinate with production and project management teams
  • Maintain safety, quality, and operational efficiency standards

Candidates with experience in pharmaceutical manufacturing plants, regulatory affairs, clinical documentation, quality systems, production operations, and healthcare compliance may receive preference during the selection process.

Eligibility / Qualifications

Candidates applying for these pharmaceutical vacancies should possess relevant educational qualifications and healthcare industry experience.

Required Qualification

Eligible qualifications include:

  • B.Pharm
  • M.Pharm
  • ITI
  • Diploma in Engineering
  • BE
  • Relevant Technical Qualifications

Relevant Courses

B.Pharm, M.Pharm, Pharmaceutical Sciences, Industrial Pharmacy, Quality Assurance, Regulatory Affairs, Pharmaceutical Technology, Clinical Research, Pharmacovigilance, Drug Regulatory Affairs, Mechanical Engineering, Electrical Engineering, HVAC Engineering, Diploma Engineering, Industrial Training Institute (ITI)

Experience Requirement

  • Minimum 2 to 7 years of relevant pharmaceutical industry experience
  • Candidates with pharmaceutical manufacturing exposure will be preferred
  • Experience in regulated manufacturing environments may provide additional advantages

Preferred Skills

  • Strong problem-solving abilities
  • Team collaboration and coordination skills
  • Knowledge of GMP and regulatory compliance
  • Pharmaceutical documentation handling experience
  • Manufacturing and production process understanding
  • Machine operation and maintenance skills
  • Communication and reporting abilities

Candidates searching for pharma walk-in interviews, pharmaceutical company jobs in Tamil Nadu, quality assurance executive jobs, regulatory affairs careers, production officer vacancies, QC executive openings, and healthcare manufacturing jobs can attend this recruitment drive.

Location & Salary

Job Location

Kanchipuram

Salary

Salary will be offered based on candidate experience, qualifications, technical expertise, and company standards.

Application Process

Interested and eligible candidates can directly attend the walk-in interview or apply through email.

Walk-In Interview Details

  • Date: 10th May 2026 (Sunday)
  • Time: 09:00 AM to 02:00 PM

Interview Venue

SunGlow Lifescience Private Limited 8th Floor, Kaleesuwary Towers, No 10/98A, Pace Aagam Apartments, Velachery Main Road, Ranganathapuram, Medavakkam, Chennai – 600100, Tamil Nadu, India

Factory Location

SunGlow Lifescience Pvt. Ltd. Kattankulam Village, Uthiramerur Taluk, Kancheepuram District – 631606

Apply Through Email

Official Website

Contact Number

  • +91 94999 53550

Documents Required

Candidates attending the walk-in interview should carry:

  • Updated Resume
  • Educational Certificates
  • Experience Certificates
  • Recent Passport Size Photographs
  • Government ID Proof
  • Latest Salary Documents

Applicants are advised to attend the interview early to avoid delays during the selection process.

FAQs

1. What is the interview date for SunGlow Lifescience recruitment?

The walk-in interview is scheduled for 10th May 2026.

2. What qualifications are required for these pharma jobs?

Candidates with B.Pharm, M.Pharm, ITI, Diploma, BE, and relevant technical qualifications can apply.

3. How much experience is required?

Candidates should have 2 to 7 years of relevant pharmaceutical industry experience.

4. Which departments are hiring at SunGlow Lifescience?

The company is hiring for QA, Regulatory Affairs, Maintenance, Machine Operations, FRD, Production, Packing, QC, ARD, and Project Management departments.

5. What is the job location?

The job location is Kanchipuram, Tamil Nadu.

6. How can candidates apply for these vacancies?

Candidates can attend the walk-in interview directly or send their resume to hr@sunglowlifescience.com.

Summary Table

Company SunGlow Lifescience Private Limited
Department Vacancies QA, Regulatory Affairs, Maintenance, Machine Operators, FRD, Production & Packing, QC & ARD, Project Management
Qualification B.Pharm, M.Pharm, ITI, Diploma, BE
Experience 2 to 7 Years
Location Kanchipuram, Tamil Nadu
SunGlow Walk-In QA, Production, QC & Regulatory Affairs (1)
SunGlow Walk-In QA, Production, QC & Regulatory Affairs (1)

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