QC Specialist HPLC

Plant Location International; Hyderabad; Sur place; INR 600 000 - 900 000; Plein temps

Résumé du poste

Plant Location International is seeking a QC Specialist HPLC for an on-site, full-time role in Hyderabad. The candidate will perform routine and non-routine QC testing using HPLC and GC, prepare samples, and maintain instruments. Documentation of results and data review for trends are essential.

Collaborative work with production, QA, and regulatory teams is required to resolve quality issues and support method validation or transfer under GMP standards.

Qualifications

• Bachelors or masters in Chemistry, Pharmacy, Biotechnology, or related field.
• Experience in pharmaceutical QC lab with HPLC preferred.
• Strong documentation practices and attention to detail.
• GMP knowledge and QA principles.
• Effective communication and teamwork in regulated environments.

Responsabilités

• Perform routine and non-routine QC testing using HPLC and GC.
• Prepare samples and reagents; operate and maintain HPLC instruments.
• Document test results and review data for trends or deviations.
• Collaborate with production, QA, and regulatory teams to resolve quality issues.
• Support method validation or transfer and ensure GMP compliance.

Connaissances

Quality Control

HPLC

Data Interpretation

Quality Assurance

GMP Knowledge

Quality Auditing

Lab Documentation

Teamwork

Formation

Bsc Chemistry

MSc Chemistry

Pharmacy

Biotechnology

Outils

LIMS

Electronic Data Systems

Description du poste

Company Description

Plant Location International is a globally active company. The company values technical expertise, adherence to regulatory requirements, and continuous improvement in manufacturing environments. Professionals joining Plant Location International can expect a structured, quality-driven work culture with opportunities to contribute to global operations.

Role Description

The QC Specialist HPLC role is a full-time, on-site position based in Hyderabad. The specialist is responsible for performing routine and non-routine quality control testing using HPLC and GC instruments related analytical techniques to ensure that raw materials, in-process samples, and finished products meet defined specifications. Daily activities include preparing samples and reagents, operating and maintaining HPLC instruments, documenting test results accurately, and reviewing data for trends or deviations. The role involves collaborating with production, QA, and regulatory teams to resolve quality issues, supporting method validation or transfer, and ensuring compliance with GMP and internal quality standards. The QC Specialist also participates in investigations, audits, and continuous improvement initiatives to strengthen analytical reliability and process robustness.

Qualifications

• Candidates should possess strong Quality Control skills, including hands-on HPLC analysis and interpretation of analytical data.
• Candidates should possess Quality Assurance and Quality Management skills to support consistent compliance with internal and external standards.
• Candidates should possess knowledge of Good Manufacturing Practice (GMP) and the ability to apply GMP principles in laboratory and production environments.
• Candidates should possess Quality Auditing skills to assist with internal audits, documentation reviews, and corrective action follow-up.
• Candidates should have a bachelor’s or master’s degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field.
• Candidates should have experience in a pharmaceutical, biopharmaceutical, or chemical manufacturing QC laboratory, preferably with HPLC as a core technique.
• Candidates should demonstrate strong documentation practices, attention to detail, and familiarity with lab information management or electronic data systems.
• Candidates should have effective communication and teamwork skills and the ability to work in a structured, regulated environment.