QA / QC Executive - Male candidates Only

Vimta Labs Ltd.; Shamirpet mandal; Sur place; INR 480 000 - 720 000; Plein temps

Résumé du poste

Vimta Labs Ltd. in Shameerpet, Hyderabad, is seeking a QA/QC Executive/Analyst with 2–4 years of experience in pharmaceutical QA/QC roles.

The role involves operating and reviewing analytical data (LC-MS, GC-MS, HPLC, GC, UV, dissolution) and performing audit trail reviews using Empower/OpenLab/Chromeleon. You will ensure data integrity and support audits, with flexibility to work across QA, QC, or data review as needed.

Qualifications

• Requires B.Pharm / M.Pharm / M.Sc. (Chemistry) with pharma QA/QC exposure.
• Strong command of LC-MS/GC-MS and related data systems (LIMS/ELN).
• Knowledge of ICH Q2, ICH Q9 and GxP guidelines.

Responsabilités

• Operate and review data/chromatograms from LC-MS, GC-MS, HPLC, GC, UV, and dissolution systems.
• Perform audit trail reviews using Empower, OpenLab, or Chromeleon.
• Support compliance audits and review calibration and method validation protocols.
• Adapt to QA, QC, or Data Review roles per plant needs.

Connaissances

LC-MS

GC-MS

LIMS

ELN

ICH Q2

ICH Q9

GxP

Detail-oriented

Critical thinking

Problem-solving

Clear communication

Formation

B.Pharm / M.Pharm / M.Sc. (Chemistry)

Outils

Empower

OpenLab

Chromeleon

Description du poste

Job Title: QA / QC Executive / Analyst
Company: Vimta Labs
Location: Shameerpet, Hyderabad
Experience: 2 to 4 years
Education: B.Pharm / M.Pharm / M.Sc. (Chemistry)
Gender Preference: Male candidates only

Core Responsibilities

• Analytical & Audit Trail Review: Operate and review data/chromatograms from LC-MS, GC-MS, HPLC, GC, UV, and dissolution apparatus. Perform audit trail reviews using software like Empower, OpenLab, or Chromeleon.
• QMS & Documentation: Prepare and review QMS elements including Deviations, OOS, OOT, CAPA, Change Controls, and SOPs.
• Compliance & Audits: Ensure absolute data integrity and support internal/external regulatory audits. Review calibration and method validation protocols.
• Cross-Functional Operations: Adapt flexibly to roles across Quality Assurance, Quality Control, or Data Review based on plant requirements.

Key Requirements & Skills

• Technical: Strong command over LC-MS, GC-MS, LIMS, ELN, and standard chromatography software. Sound knowledge of ICH Q2, ICH Q9, and GxP guidelines.
• Soft Skills: Detail-oriented, strong critical thinking, proactive problem-solving, and clear communication with cross-functional teams.
• Flexibility: Must be fully willing to work in rotational shifts (including night shifts) and extend hours during audit deadlines.