Job Description
Executive – DQA Department | HOF Pharma | Sanand, Gujarat, India
HOF Pharma is hiring professionals for the role of Executive – DQA for its pharmaceutical quality assurance operations located in Sanand, Gujarat, India. This full-time opportunity is ideal for candidates with 5 to 6 years of experience in DQA operations, documentation review workflows, quality assurance activities, compliance systems, SOP management operations, audit coordination workflows, reporting systems, and regulated pharmaceutical environments.
The selected candidate will support documentation quality assurance and compliance coordination activities associated with pharmaceutical manufacturing systems and operational workflows. Responsibilities include monitoring DQA workflows and quality systems, maintaining quality records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring compliance systems and SOP workflows, ensuring adherence to GMP procedures and quality standards, preparing quality reports and operational documentation, assisting in troubleshooting and QA coordination workflows, participating in audit review and compliance activities, supporting documentation management systems, and maintaining continuous improvement of QA operations and compliance efficiency.
This role offers valuable exposure to pharmaceutical DQA systems, documentation workflows, audit coordination activities, technical documentation systems, compliance operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in quality assurance careers can strengthen their technical and operational expertise through this opportunity.
Location
Sanand, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
5 to 6 Years
About HOF Pharma
HOF Pharma operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, documentation quality workflows, compliance coordination activities, and healthcare product operations.
Key Responsibilities
Support DQA and compliance coordination activities.
Monitor quality systems and documentation workflows.
Maintain quality records and technical documentation.
Coordinate with QA and production teams.
Monitor compliance systems and SOP activities.
Ensure adherence to GMP procedures and quality standards.
Prepare quality reports and operational documentation.
Support troubleshooting and QA coordination workflows.
Participate in audit review and compliance activities.
Assist in continuous improvement of QA systems.
Required Skills
Strong knowledge of DQA and pharmaceutical QA operations.
Understanding of GMP systems and compliance workflows.
Knowledge of SOP management and audit activities.
Experience in documentation review and reporting systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of pharmaceutical QA standards and systems.
Ability to manage documentation schedules and workflows.
Attention to documentation accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc / B.Pharm / M.Pharm
Industry
Pharmaceutical
Why Join HOF Pharma?
HOF Pharma offers professionals opportunities to work in advanced pharmaceutical environments with exposure to QA systems, documentation workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this Executive – DQA opportunity by submitting their updated resume and relevant documents.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.
HOF Pharma is hiring professionals for the role of Executive – DQA for its pharmaceutical quality assurance operations located in Sanand, Gujarat, India. This full-time opportunity is ideal for candidates with 5 to 6 years of experience in DQA operations, documentation review workflows, quality assurance activities, compliance systems, SOP management operations, audit coordination workflows, reporting systems, and regulated pharmaceutical environments.
The selected candidate will support documentation quality assurance and compliance coordination activities associated with pharmaceutical manufacturing systems and operational workflows. Responsibilities include monitoring DQA workflows and quality systems, maintaining quality records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring compliance systems and SOP workflows, ensuring adherence to GMP procedures and quality standards, preparing quality reports and operational documentation, assisting in troubleshooting and QA coordination workflows, participating in audit review and compliance activities, supporting documentation management systems, and maintaining continuous improvement of QA operations and compliance efficiency.
This role offers valuable exposure to pharmaceutical DQA systems, documentation workflows, audit coordination activities, technical documentation systems, compliance operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in quality assurance careers can strengthen their technical and operational expertise through this opportunity.
Location
Sanand, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
5 to 6 Years
About HOF Pharma
HOF Pharma operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, documentation quality workflows, compliance coordination activities, and healthcare product operations.
Key Responsibilities
Support DQA and compliance coordination activities.
Monitor quality systems and documentation workflows.
Maintain quality records and technical documentation.
Coordinate with QA and production teams.
Monitor compliance systems and SOP activities.
Ensure adherence to GMP procedures and quality standards.
Prepare quality reports and operational documentation.
Support troubleshooting and QA coordination workflows.
Participate in audit review and compliance activities.
Assist in continuous improvement of QA systems.
Required Skills
Strong knowledge of DQA and pharmaceutical QA operations.
Understanding of GMP systems and compliance workflows.
Knowledge of SOP management and audit activities.
Experience in documentation review and reporting systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of pharmaceutical QA standards and systems.
Ability to manage documentation schedules and workflows.
Attention to documentation accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc / B.Pharm / M.Pharm
Industry
Pharmaceutical
Why Join HOF Pharma?
HOF Pharma offers professionals opportunities to work in advanced pharmaceutical environments with exposure to QA systems, documentation workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this Executive – DQA opportunity by submitting their updated resume and relevant documents.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.