Instagram
youtube
Facebook

Senior Executive Quality Assurance

3-5 years
Not Disclosed
10 June 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Summary

We are hiring a Senior Executive – Quality Assurance (QA) for our liquid injectable facility located in Baddi, India. This role involves ensuring cGMP compliance, process validation, batch manufacturing review, and documentation control in a regulated pharmaceutical environment. The candidate will be responsible for maintaining quality systems, supporting deviation handling, and coordinating cross-functional activities to ensure consistent product quality and regulatory adherence.


Key Responsibilities

  • Conduct line clearance at various stages of batch manufacturing and packing.

  • Verify materials during the dispensing process for liquid injectable products.

  • Monitor manufacturing processes in line with BMR (Batch Manufacturing Record) and BPR (Batch Packaging Record).

  • Perform In-Process Quality Checks as per defined protocols.

  • Collect in-process, control, stability, validation, and other required samples.

  • Maintain control samples and related documentation.

  • Manage issuance and control of BMR and BPR for the liquid injectable facility.

  • Execute validation and qualification activities.

  • Ensure adherence to cGMP guidelines and implement CAPA when necessary.

  • Log change controls and deviations and maintain associated records.

  • Compile investigation reports and support cross-functional teams for resolution and closure.

  • Handle market complaint logging and initiate investigations.

  • Review and approve cross-functional quality documents.

  • Review batch manufacturing and packing records prior to batch release.


Required Skills & Qualifications

  • Degree/Diploma in Pharmacy, Chemistry, or related scientific field (not specified in JD).

  • Experience in Quality Assurance, preferably in liquid injectable manufacturing.

  • Strong understanding of cGMP, BMR, BPR, and validation activities.

  • Familiarity with deviation management, CAPA implementation, and change control processes.

  • Excellent documentation, coordination, and communication skills.

  • Ability to handle cross-functional quality-related tasks.


Perks & Benefits

  • Competitive salary (Not disclosed in JD).

  • Exposure to advanced liquid injectable manufacturing processes.

  • Opportunity to work in a cGMP-compliant and regulatory-focused environment.

  • Professional development and growth opportunities in pharmaceutical quality assurance.


Company Description

A leading pharmaceutical manufacturer specializing in high-quality injectable products. The company is committed to delivering safe, effective, and compliant healthcare solutions backed by stringent quality control and regulatory practices.


Work Mode

On-site – Baddi, India


Call-to-Action

If you have the skills and passion for ensuring pharmaceutical product quality and regulatory compliance, apply now to join our Quality Assurance team at our state-of-the-art liquid injectable facility in Baddi!