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Executive Quality Assurance

Abbott
Abbott
1-3 years
Not Disclosed
10 July 4, 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

 

Executive – Quality Assurance

Location: Baddi, Himachal Pradesh, India
Category: Quality | Full-time


Job Summary:

Join a top pharmaceutical manufacturing facility in Baddi as an Executive – Quality Assurance and take charge of critical quality systems, SOP documentation, audit compliance, training coordination, and QMS implementation. This is a pivotal opportunity for QA professionals with a strong focus on documentation control, CAPA, and regulatory compliance in a fast-paced GMP-compliant environment.


Key Responsibilities:

  • Preparation, issuance, retrieval, and archival of master documents (SOPs, Specifications, STPs, Quality Manual, VMP, etc.)

  • Managing DARIUS software compliance and documentation controls

  • Handling uncontrolled master document issuance for external reference and exception closures

  • Controlling general document numbering system

  • Ensuring timely documentation of OOS (Out of Specification), Exceptions, and Change Control activities

  • QMS implementation and tracking through SolTRAQs application

  • Managing artwork compliance using Harmony platform

  • Creating and updating Maximum Retail Price (MRP) lists

  • Preparing Annual Product Quality Review (APQR) reports and identifying improvement areas

  • Conducting CAPA effectiveness checks and audit follow-ups

  • Designing training materials and coordinating GMP/technical trainings using ISOtrain

  • Managing training data updates, past-due follow-ups, and reconciliation in ISOtrain

  • Maintaining records of QA and cross-functional training activities

  • Adhering to site safety standards and the Code of Business Conduct (COBC)

  • Performing miscellaneous QA tasks as assigned by seniors


Required Skills & Qualifications:

  • Bachelor’s degree in Pharmacy, Life Sciences, or equivalent

  • 1–3 years of experience in pharmaceutical quality assurance

  • Proficient in QMS tools, SOP and documentation practices

  • Working knowledge of DARIUS and ISOtrain systems preferred

  • Familiarity with SolTRAQs and Harmony software a plus

  • Strong understanding of GMP, OOS handling, and CAPA documentation

  • Good communication and coordination skills for cross-functional collaboration

  • Detail-oriented with excellent documentation and compliance abilities


Perks & Benefits:

  • Competitive salary (not specified)

  • Structured career growth in pharma quality roles

  • On-the-job training and ISOtrain-based learning

  • Health and wellness benefits as per company policy

  • Exposure to regulatory audits and global quality systems

  • Safe and compliant workplace culture


Company Description:

This opportunity is with a leading pharmaceutical manufacturer in Baddi, committed to delivering high-quality healthcare solutions. With robust quality systems and regulatory compliance, the company ensures global standards in drug production and employee development.


Work Mode: On-site (Baddi, Himachal Pradesh)


Salary Range: Not specified in the job description


Call to Action:

Ready to elevate your career in pharmaceutical quality assurance? Apply now to be a part of a high-impact QA team ensuring excellence in pharma manufacturing and compliance.