Nectar Lifesciences Pvt Ltd Hiring for QA (Validation) Officer Role – Pharma Apply on Rasayanika

Pharma Jobs in QC at Nectar Lifesciences Pvt Ltd

Company name : Nectar Lifesciences Pvt Ltd

Job Title : Quality Assurance (Validation) Officer

Location : Himachal Pradesh (Solan)

Employment Type : Full-time

Qualification : B.Pharma candidates

Gender Preference : No such preference

Salary : ₹4.2 lakh to ₹4.8 lakh

Job Summary:

The QA (Validation) professional will be responsible for ensuring that all validation activities related to equipment, utilities, cleaning, analytical methods, and computer systems comply with cGMP, regulatory guidelines (USFDA, MHRA, WHO, EU), and Nectar Lifesciences’ internal quality standards. The role will involve planning, execution, review, and approval of validation protocols and reports to ensure a robust state of control.

Key Responsibilities:

Drafting, reviewing, and approving validation protocols & reports for:

• Process Validation (PV)

• Cleaning Validation (CV)

• Equipment & Utility Qualification (IQ/OQ/PQ)

• Analytical Method Validation (AMV)

• Computer System Validation (CSV)

Ensuring compliance with cGMP and ICH Q7/Q8/Q9/Q10 guidelines.
Monitoring and trending of critical process parameters (CPPs) and critical quality attributes (CQAs).
Coordinating with Production, QC, and Engineering teams for validation activities.
Ensuring timely execution of periodic reviews & re-validation as per regulatory requirements.
Handling deviation, change control, and CAPA related to validation activities.
Supporting regulatory inspections & customer audits with complete validation documentation.
Maintaining and updating validation-related SOPs and training for QA/production staff.

Requirements:

• Education: B.Pharma, M.Pharma candidates

• Experience: 4–8 years exp

Skills:

Technical & Regulatory Knowledge

• In-depth understanding of cGMP, GLP, and ICH guidelines.

• Familiarity with USFDA, MHRA, WHO, and EU regulatory requirements.

• Strong knowledge of validation lifecycle (Installation Qualification, Operational Qualification, Performance Qualification).

Validation Expertise

• Hands-on experience in equipment, utility, process, cleaning, and computer system validation.

• Drafting and reviewing validation protocols (IQ/OQ/PQ) and reports.

• Proficiency in risk assessment & impact analysis for validation activities.

• Understanding of data integrity and ALCOA+ principles.

Documentation & QMS

• Expertise in SOP preparation, deviation handling, CAPA, and change control.

• Knowledge of LIMS and electronic documentation systems.

• Strong technical writing and documentation accuracy.

Analytical & Problem-Solving

• Ability to troubleshoot validation failures and suggest corrective measures.

• Competence in reviewing analytical data related to method validation.

• Risk-based thinking for validation planning.

Interview Process:

• Mode: Direct Interview

• Rounds: 3 Rounds

CLICK HERE TO APPLY ONLINE 

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