Job Description
DQA Officer – Quality Assurance Department | SynZeal Research Pvt. Ltd. | Ahmedabad, Gujarat, India
SynZeal Research Pvt. Ltd. is hiring professionals for the role of DQA Officer for its pharmaceutical quality assurance operations located in Ahmedabad, Gujarat, India. This full-time opportunity is ideal for candidates with 1 to 5 years of experience in data quality assurance operations, documentation review workflows, GMP compliance activities, QA systems, audit coordination operations, quality documentation systems, SOP implementation activities, compliance reporting workflows, and regulated pharmaceutical industry environments.
The selected candidate will support data quality assurance and compliance activities associated with pharmaceutical manufacturing systems and GMP-regulated workflows. Responsibilities include reviewing quality documents and operational records, maintaining DQA records and compliance documentation, coordinating with QA and production teams for operational support activities, monitoring documentation workflows and quality systems, ensuring adherence to SOP procedures and regulatory standards, preparing audit reports and operational documentation, assisting in troubleshooting and DQA coordination workflows, participating in compliance review and validation activities, supporting quality improvement initiatives, and maintaining continuous improvement of pharmaceutical quality systems and documentation operations.
This role offers valuable exposure to pharmaceutical QA systems, documentation workflows, compliance operations, audit coordination activities, validation systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in data quality assurance careers can strengthen their technical and operational expertise through this opportunity.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
1 to 5 Years
About SynZeal Research Pvt. Ltd.
SynZeal Research Pvt. Ltd. operates in the pharmaceutical industry specializing in pharmaceutical quality systems, research operations, GMP workflows, analytical support services, and regulated pharmaceutical solutions.
Key Responsibilities
Support DQA and compliance management activities.
Review operational records and quality documentation.
Maintain DQA records and compliance systems.
Coordinate with QA and production teams.
Monitor documentation workflows and quality systems.
Ensure adherence to SOP procedures and regulatory standards.
Prepare audit reports and operational documentation.
Support troubleshooting and DQA coordination workflows.
Participate in validation and compliance review activities.
Assist in continuous improvement of quality systems.
Required Skills
Strong knowledge of QA and documentation operations.
Understanding of GMP compliance and quality systems.
Knowledge of SOP implementation and audit workflows.
Experience in documentation review and reporting activities.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of regulatory standards and QA systems.
Ability to manage documentation schedules and workflows.
Attention to compliance accuracy and documentation standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc Organic Chemistry
Industry
Pharmaceutical
Why Join SynZeal Research Pvt. Ltd.?
SynZeal Research Pvt. Ltd. offers professionals opportunities to work in regulated pharmaceutical environments with exposure to QA systems, documentation workflows, compliance operations, and research support activities.
How to Apply
Interested candidates can apply through ACKJOBS for this DQA Officer 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.
SynZeal Research Pvt. Ltd. is hiring professionals for the role of DQA Officer for its pharmaceutical quality assurance operations located in Ahmedabad, Gujarat, India. This full-time opportunity is ideal for candidates with 1 to 5 years of experience in data quality assurance operations, documentation review workflows, GMP compliance activities, QA systems, audit coordination operations, quality documentation systems, SOP implementation activities, compliance reporting workflows, and regulated pharmaceutical industry environments.
The selected candidate will support data quality assurance and compliance activities associated with pharmaceutical manufacturing systems and GMP-regulated workflows. Responsibilities include reviewing quality documents and operational records, maintaining DQA records and compliance documentation, coordinating with QA and production teams for operational support activities, monitoring documentation workflows and quality systems, ensuring adherence to SOP procedures and regulatory standards, preparing audit reports and operational documentation, assisting in troubleshooting and DQA coordination workflows, participating in compliance review and validation activities, supporting quality improvement initiatives, and maintaining continuous improvement of pharmaceutical quality systems and documentation operations.
This role offers valuable exposure to pharmaceutical QA systems, documentation workflows, compliance operations, audit coordination activities, validation systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in data quality assurance careers can strengthen their technical and operational expertise through this opportunity.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
1 to 5 Years
About SynZeal Research Pvt. Ltd.
SynZeal Research Pvt. Ltd. operates in the pharmaceutical industry specializing in pharmaceutical quality systems, research operations, GMP workflows, analytical support services, and regulated pharmaceutical solutions.
Key Responsibilities
Support DQA and compliance management activities.
Review operational records and quality documentation.
Maintain DQA records and compliance systems.
Coordinate with QA and production teams.
Monitor documentation workflows and quality systems.
Ensure adherence to SOP procedures and regulatory standards.
Prepare audit reports and operational documentation.
Support troubleshooting and DQA coordination workflows.
Participate in validation and compliance review activities.
Assist in continuous improvement of quality systems.
Required Skills
Strong knowledge of QA and documentation operations.
Understanding of GMP compliance and quality systems.
Knowledge of SOP implementation and audit workflows.
Experience in documentation review and reporting activities.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of regulatory standards and QA systems.
Ability to manage documentation schedules and workflows.
Attention to compliance accuracy and documentation standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc Organic Chemistry
Industry
Pharmaceutical
Why Join SynZeal Research Pvt. Ltd.?
SynZeal Research Pvt. Ltd. offers professionals opportunities to work in regulated pharmaceutical environments with exposure to QA systems, documentation workflows, compliance operations, and research support activities.
How to Apply
Interested candidates can apply through ACKJOBS for this DQA Officer 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.