Quality Control Manager OSD

Moola Global Bangalore; Visakhapatnam; Presencial; INR 600.000 - 900.000; Jornada completa

Descripción de la vacante

We are hiring an experienced Quality Control Manager for a growing nutraceutical manufacturing organization in Visakhapatnam. The role involves leading QC laboratory operations, managing analytical testing, ensuring regulatory compliance, and establishing robust laboratory systems for a greenfield manufacturing facility.

The ideal candidate should have strong hands-on experience in HPLC, analytical testing, laboratory documentation, and QC team management, preferably within the nutraceutical,

Formación

• Experience in regulated QC laboratory environment.
• 5–12 years of QC or QC laboratory experience.
• Hands-on experience with HPLC and analytical testing.
• Strong knowledge of laboratory operations.
• Experience in OOS/OOT investigations, deviations, CAPA, and data integrity.

Responsabilidades

• Lead and manage day-to-day Quality Control laboratory operations.
• Supervise QC analysts, officers, microbiology staff and other laboratory personnel.
• Oversee testing of raw materials, packaging materials, in-process samples and finished products.
• Review and approve analytical results, specifications, CoA.
• Operate and oversee laboratory instruments including HPLC, UV-Vis, dissolution, moisture analyzers.
• Ensure compliance with cGMP, GLP, GDP, and data integrity requirements.
• Handle OOS and OOT investigations, deviations, and CAPA.
• Manage analytical method validation, verification, and transfer activities.
• Plan and monitor stability studies and shelf-life assessments.
• Develop and maintain QC SOPs, documentation, and data integrity systems.
• Coordinate and support regulatory, customer, and third-party audits.
• Oversee microbiological testing and related QC activities.
• Establish QC performance indicators and improve laboratory efficiency.
• Coordinate with Production, QA, Engineering, Warehouse, Regulatory, and Microbiology teams.
• Support the development and implementation of QC systems in a greenfield manufacturing environment.

Conocimientos

HPLC

Analytical testing

Lab operations

OOS/OOT investigations

Deviations

CAPA

Data integrity

Method validation

Method verification

Method transfer

Stability studies

Lab documentation

QC team leadership

Laboratory management

cGMP

GLP

GDP

Regulatory compliance

Regulatory requirements

Laboratory systems

Educación

Pharmacy / Chemistry

Descripción del empleo

Job Title: Quality Control Manager Nutraceuticals

Job Location: Visakhapatnam (Vizag), Andhra Pradesh
Industry: Nutraceuticals / Pharmaceuticals / Food Manufacturing
Experience: 5-12 Years
Salary: 6-9 LPA (Depending on Experience)
Employment Type: Full-Time, Permanent
Department: Quality Control

Job Summary

We are hiring an experienced Quality Control Manager for a growing nutraceutical manufacturing organization in Visakhapatnam. The role involves leading QC laboratory operations, managing analytical testing, ensuring regulatory compliance, and establishing robust laboratory systems for a greenfield manufacturing facility.

The ideal candidate should have strong hands-on experience in HPLC, analytical testing, laboratory documentation, and QC team management, preferably within the nutraceutical, pharmaceutical, or food manufacturing industry.

Key Responsibilities

• Lead and manage day-to-day Quality Control laboratory operations.
• Supervise QC analysts, officers, microbiology personnel, and other laboratory staff.
• Oversee the testing of raw materials, packaging materials, in-process samples, and finished products.
• Review and approve analytical results, specifications, laboratory worksheets, and Certificates of Analysis (CoA).
• Operate and oversee laboratory instruments, including HPLC, UV-Visible Spectrophotometer, dissolution apparatus, and moisture analysers.
• Ensure compliance with cGMP, GLP, GDP, data integrity requirements, and applicable regulatory standards.
• Handle Out of Specification (OOS) and Out of Trend (OOT) investigations, deviations, and Corrective and Preventive Actions (CAPA).
• Manage analytical method validation, method verification, and method transfer activities.
• Plan and monitor stability studies and shelf-life assessments.
• Develop and maintain QC laboratory SOPs, documentation, and data integrity systems.
• Coordinate and support regulatory, customer, and third-party audits.
• Oversee microbiological testing and related QC activities.
• Establish QC performance indicators and continuously improve laboratory efficiency and productivity.
• Coordinate with Production, Quality Assurance, Engineering, Warehouse, Regulatory, and Microbiology teams.
• Support the development and implementation of QC systems in a greenfield manufacturing environment.

Required Skills

• Hands-on experience with HPLC and analytical laboratory instruments.
• Strong knowledge of analytical testing and laboratory operations.
• Experience in OOS/OOT investigations, deviations, CAPA, and data integrity.
• Knowledge of analytical method validation, verification, and transfer.
• Experience in stability studies and laboratory documentation.
• QC team handling and laboratory management skills.
• Understanding of cGMP, GLP, GDP, and applicable regulatory requirements.
• Ability to establish laboratory systems and work hands-on in a growing organization.

Educational Qualification

Relevant qualification in Pharmacy, Chemistry, or a related scientific discipline, with experience in a regulated laboratory environment.

Candidate Profile

• 5-12 years of relevant experience in Quality Control or QC laboratory functions.
• Strong hands-on laboratory exposure is essential.
• HPLC experience is mandatory.
• Previous experience managing or supervising QC personnel is required.
• Nutraceutical manufacturing experience is preferred.
• Candidates from pharmaceutical or food manufacturing backgrounds may also apply.
• Candidates should be comfortable building and strengthening QC laboratory systems in a growing manufacturing organization.