Arene Lifesciences Walk-In Interview 2026 | QA QC Production Jobs

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Arene Lifesciences Walk-In Interview 2026 – Multiple Pharma Jobs in Telangana

Arene Lifesciences Limited is conducting a walk-in recruitment drive from September 19 to September 27, 2026, for professionals across Production, Quality Control, Quality Assurance, Engineering, Process Development and Corporate Quality functions.

The openings cover a wide range of experience levels, from 1 year to 14 years, making the drive relevant to both early-career professionals and experienced pharmaceutical specialists.

The positions are associated with Arene’s manufacturing and quality operations in Nalgonda and Sangareddy, Telangana.

Job Overview

Details Information
Company Arene Lifesciences Limited
Industry API & Bulk Drug Manufacturing
Departments Production, QC, QA, Engineering, Process Development
Experience 1–14 Years
Locations Nalgonda & Sangareddy, Telangana
Work Type Full-time / On-site
Interview Type Walk-In
Interview Dates September 19–27, 2026

About Arene Lifesciences

Arene Lifesciences Limited operates in the API and bulk drug manufacturing sector, with manufacturing facilities in Telangana.

The company’s recruitment drive covers technical and quality functions supporting pharmaceutical manufacturing, analytical testing, quality systems, engineering operations and process development.

Professionals joining these teams can work across areas such as cGMP manufacturing, analytical testing, QMS, IPQA, batch release, engineering utilities and process development.

Arene Lifesciences Current Openings

1. Production Chemist / Senior Chemist

Department: Production – API/Bulk Drugs
Experience: 2–5 Years

The role involves supporting API manufacturing activities, monitoring production processes and maintaining manufacturing documentation according to approved procedures.

2. Pressure Reactor Handler

Department: Production – API/Bulk Drugs
Experience: 2–5 Years

Candidates with hands-on experience operating or handling pressure reactors in pharmaceutical or chemical manufacturing environments can apply.

3. Clean Room & Packing Specialist

Department: Production / Clean Room Operations
Experience: 2–5 Years

The position covers clean-room activities, documentation and pharmaceutical packing operations.

4. Engineering & Maintenance Specialist

Department: Engineering & Maintenance
Experience: 2–5 Years

Relevant areas include:

  • Plant maintenance
  • AHU systems
  • RO water systems
  • Utility operations
  • Equipment troubleshooting

5. QC Executive – Microbiology & Instrumentation

Department: Quality Control
Experience: 2–5 Years

The role involves laboratory and quality-control activities, including microbiology and analytical instrumentation.

6. IPQA Executive

Department: Quality Assurance
Experience: 2–5 Years

The position focuses on in-process quality assurance, manufacturing-floor compliance and documentation.

7. Process Development Chemist

Department: Process Development Lab
Experience: 1–2 Years

Candidates will support process development laboratory activities, experimentation and technical documentation.

8. Assistant Manager / Deputy Manager – Corporate QA

Department: Corporate Quality Assurance
Experience: 8–14 Years

Key Areas

  • Quality Management Systems
  • Batch release
  • Corporate quality oversight
  • Compliance and documentation
  • Audit readiness

9. Senior QC Executive

Department: Quality Control
Experience: 5–8 Years

Key Areas

  • QMS
  • Analytical Method Validation
  • HPLC
  • GC
  • Analytical testing
  • Documentation and data review

10. QA Executive – QMS / IPQA / AQA

Department: Quality Assurance
Experience: 3–8 Years

The position covers quality systems, in-process quality assurance and analytical quality assurance activities.

11. Assistant Manager / Deputy Manager – QA/QC

Department: QA / QC
Experience: 3–8+ Years

Experienced quality professionals can apply for management-level positions based on their relevant technical and pharmaceutical experience.

Skills & Technical Requirements

Depending on the position, candidates should have experience in relevant areas such as:

  • API and bulk drug manufacturing
  • Pressure reactor operations
  • Clean-room operations
  • HPLC
  • GC
  • Wet chemistry
  • Analytical Method Validation
  • QMS
  • IPQA
  • AQA
  • Batch release
  • LIMS
  • AHU systems
  • RO water systems
  • Pharmaceutical documentation
  • cGMP compliance
  • Audit readiness

Candidates should highlight their hands-on experience and specific technical skills clearly in their resumes.

Key Responsibilities

Responsibilities vary according to the position, but may include:

Production

  • Execute API manufacturing processes according to approved procedures
  • Monitor critical process parameters
  • Handle production equipment and reactors
  • Maintain batch records and manufacturing documentation
  • Follow cGMP and safety requirements
  • Support production efficiency and troubleshooting

Quality Control

  • Perform raw-material and in-process testing
  • Conduct analytical testing using HPLC and GC
  • Perform method validation activities
  • Support stability and quality testing
  • Maintain laboratory records
  • Ensure compliance with applicable GMP and GLP requirements

Quality Assurance

  • Perform IPQA activities
  • Manage QMS documentation
  • Review manufacturing records
  • Support batch-release activities
  • Handle deviations, CAPA and change controls
  • Maintain audit-ready documentation

Engineering

  • Operate and maintain AHU systems
  • Manage RO and other water systems
  • Perform preventive and breakdown maintenance
  • Troubleshoot plant equipment
  • Maintain utility documentation and records

Who Can Apply?

The recruitment drive is intended for professionals with relevant qualifications and pharmaceutical/chemical industry experience.

Depending on the position, suitable backgrounds may include:

  • Chemistry
  • Pharmacy
  • Microbiology
  • Biotechnology
  • Chemical Engineering
  • Mechanical/Engineering disciplines
  • Pharmaceutical sciences

Experience requirements range from 1–14 years, depending on the position.

Immediate joiners are encouraged to check the role requirements before attending.

Walk-In Interview Details

Venue 1 – QC & QA | Unit-2

Dates: September 19–27, 2026

Venue:
Arene Lifesciences (Unit-2) Pvt. Ltd.
Sy. No. 412/A
Veliminedu Village, Chityal (M)
Nalgonda District, Telangana – 508114

Contact: +91 7674889921
Email: humanresources.u2@arenelife.com

Venue 2 – Corporate QA, QC & Management Roles

Dates: September 19–27, 2026

Venue:
Arene Lifesciences Pvt. Ltd.
Sy. No. 48–50, 209–211, IDA II
Pashamylaram Village
Patancheru (M)
Sangareddy District, Telangana – 502307

Contact: +91 7674888964
Email: humanresources@arenelife.com

Documents to Carry

Candidates attending the walk-in should carry:

  • Updated Resume/CV
  • Educational certificates
  • Experience certificates
  • Recent salary slips
  • Government-issued photo ID
  • Relevant employment documents

Experienced candidates should ensure their CV clearly mentions their current role, total experience and technical expertise.

How to Apply

Attend the Walk-In Interview

Eligible candidates can directly attend the appropriate venue during the recruitment period.

Unable to Attend?

Candidates who cannot attend in person can send their updated resume to:

humanresources@arenelife.com

or

humanresources.u2@arenelife.com

Mention the position and department in the email subject line.

Career Benefits & Exposure

The advertised roles provide exposure to areas such as:

  • API and bulk drug manufacturing
  • Modern analytical instrumentation
  • Pharmaceutical quality systems
  • LIMS and digital documentation
  • Process development
  • Engineering utilities
  • Regulatory compliance
  • Technical and professional development

Salary and specific employment benefits should be confirmed with the Arene Lifesciences recruitment team for the individual position.

Interview Preparation Tips

Before attending the interview, candidates should revise topics relevant to their department.

For Production Roles

  • API manufacturing processes
  • Reactor operations
  • cGMP
  • Batch documentation
  • Process safety
  • Clean-room practices

For QC Roles

  • HPLC and GC
  • Method validation
  • Wet analysis
  • Stability testing
  • OOS/OOT concepts
  • GMP/GLP

For QA Roles

  • IPQA
  • QMS
  • CAPA
  • Deviations
  • Change control
  • Batch release
  • Audit readiness

For Engineering Roles

  • AHU systems
  • RO water systems
  • Preventive maintenance
  • Utility operations
  • Equipment troubleshooting

Frequently Asked Questions

1. When is the Arene Lifesciences walk-in interview?

The recruitment drive is scheduled from September 19 to September 27, 2026.

2. Which departments are hiring?

Openings are available across Production, Quality Control, Quality Assurance, Engineering, Process Development and Corporate Quality.

3. What experience is required?

Experience requirements range from 1 to 14 years, depending on the position.

4. Where are the job locations?

The openings are associated with facilities in Nalgonda and Sangareddy, Telangana.

5. What qualifications are accepted?

Relevant qualifications in Chemistry, Pharmacy, Microbiology, Biotechnology and Engineering may be considered according to the position.

6. Can immediate joiners apply?

Yes. The recruitment information specifically invites professionals and immediate joiners who meet the respective role requirements.

7. Can I apply if I cannot attend the walk-in?

Yes. Candidates can email their CV to humanresources@arenelife.com or humanresources.u2@arenelife.com.

8. What technical skills are useful for QC positions?

Experience with HPLC, GC, analytical method validation, wet chemistry, QMS and LIMS is relevant for the advertised QC roles.

9. What documents should I bring?

Carry your updated CV, academic certificates, experience documents, recent salary slips and government-issued ID.

Arene Lifesciences Walk-In Interview 2026

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