Neuland Laboratories Walk-In Interview on  November 1, 2025 in Hyderabad for QA, QC, and Engineering Professionals

Neuland Laboratories Announces Walk-In Interviews for Multiple Positions in Hyderabad

Opportunity for experienced professionals in pharmaceutical manufacturing to join a leading industry player

Neuland Laboratories Limited, a well-established name in the pharmaceutical manufacturing sector, has announced a walk-in recruitment drive for several key positions across its Quality Assurance, Quality Control, and Plant Engineering departments. The interviews are scheduled for November 1st, 2025 (Saturday), offering a valuable opportunity for qualified candidates to explore career growth with the company.

Interview Details:

Date: November 1, 2025 (Saturday)

Time: 10:00 AM to 4:00 PM

Venue:

PHARMA JOBS Talent Acquisition Centre, Bhagyaradhi Degree College, 1st Floor, Near IDPL X Roads, Hyderabad

Open Positions:

1. Quality Assurance

Role: AQA (Analytical Quality Assurance)

Designation: Executive

Experience: 5-8 Years

Qualification: B.Sc / M.Sc / B. Pharmacy

2. Quality Control

Role: HPLC, GC, LC-MS & ICP-MS

Designation: Officers

Experience: 4-6 Years

Qualification: B.Sc / M.Sc / B. Pharmacy

3. Plant Engineering

Mechanical Maintenance – Officer / Executive (5-8 Years, B.Tech Mechanical)

Electrical Maintenance – Officer / Executive (5-8 Years, B.Tech Electrical)

Utility – Executive (6-9 Years, B.Tech Mechanical)

Work Location:

All selected candidates will be based at Neuland Laboratories Limited, Unit-3, Gaddapotharam, Hyderabad.

Key Requirements & Benefits:

· API Pharma Experience is mandatory for all roles.

· The company is offering a competitive salary package, described as “Best in the Industry.”

· A joining bonus will be provided for candidates who join early.

Interested applicants must bring:

  · Updated CV

  · Last 2 months’ pay slips

  · Latest increment letter

📞 Contact Information:

For further details, candidates can reach out via:

Email: brohini@neulandlabs.com

Phone: 8179538447

FAQ:

1. What analytical instruments and techniques should candidates be proficient in for the Quality Control (QC) department?

Candidates applying for QC roles should have hands-on experience with advanced analytical instruments such as HPLC, GC, LC-MS, and ICP-MS. Knowledge of method validation, calibration, system suitability testing, and data integrity compliance (as per ALCOA+ principles) is essential. Experience in handling chromatographic data systems (CDS) like Empower or Chromeleon is also preferred.

2. What are the key responsibilities in the Analytical Quality Assurance (AQA) role?

AQA Executives are responsible for:

Reviewing analytical raw data, test records, and chromatographic reports.

Ensuring compliance with GMP, GLP, and data integrity requirements.

Handling OOS (Out of Specification), OOT (Out of Trend) investigations.

Supporting regulatory audits (USFDA, EMA, WHO) and maintaining audit readiness.

Coordinating with QC for document verification and analytical data review.

3. What are the main areas of focus in Plant Engineering for API manufacturing?

For Mechanical and Electrical Maintenance roles, focus areas include:

Maintenance and troubleshooting of reactors, centrifuges, dryers, and HVAC systems.

Preventive maintenance schedules and equipment calibration.

Utility systems management such as chillers, boilers, compressors, and water systems.

Implementation of energy-saving and safety practices as per GMP and EHS standards.

Experience with CMMS (Computerized Maintenance Management Systems) is an added advantage.

4. What kind of documentation and regulatory knowledge is expected in API manufacturing roles?

All candidates should have strong understanding of Good Manufacturing Practices (GMP), ICH Q7 guidelines, and regulatory documentation including:

Batch Manufacturing Records (BMR)

Equipment Qualification (IQ/OQ/PQ)

Calibration records and maintenance logs

Deviation, CAPA, and Change Control documentation

Knowledge of USFDA, MHRA, and EDQM audit requirements is preferred.

5. How can candidates prepare for the technical interview at Neuland Laboratories?

Candidates should:

Review their core subject knowledge in pharmaceutical manufacturing and analytical chemistry.

Be ready to discuss previous project experiences, instrument handling, and GMP compliance scenarios.

Understand process safety, data integrity principles, and root cause analysis (RCA).

Carry all supporting documents (CV, pay slips, increment letter) and be prepared for both technical and HR discussions during the walk-in.