Job Description
QA – Validation Executive – Quality Assurance Department | Akums Drugs & Pharmaceuticals Ltd. | Lalru, Punjab, India
Akums Drugs & Pharmaceuticals Ltd. is hiring professionals for the role of QA – Validation Executive for its pharmaceutical quality assurance operations located in Lalru, Punjab, India. This full-time opportunity is ideal for candidates with 2+ years of experience in QA validation operations, pharmaceutical compliance systems, validation documentation workflows, GMP procedures, audit coordination activities, quality assurance systems, SOP implementation, regulatory documentation, process validation workflows, and regulated pharmaceutical industry environments.
The selected candidate will support validation and quality assurance activities associated with pharmaceutical manufacturing systems and GMP operations. Responsibilities include preparing validation protocols and reports, maintaining QA records and GMP documentation, coordinating with production and QC teams for validation support activities, monitoring compliance workflows and quality systems, ensuring adherence to SOP procedures and regulatory standards, preparing audit reports and operational documentation, assisting in troubleshooting and QA coordination workflows, participating in validation review and compliance activities, supporting process qualification and operational improvement initiatives, and maintaining continuous improvement of pharmaceutical quality systems.
This role offers valuable exposure to pharmaceutical quality systems, GMP-regulated workflows, validation coordination activities, compliance operations, documentation systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in pharmaceutical QA and validation careers can strengthen their technical and operational expertise through this opportunity.
Location
Lalru, Punjab, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
2+ Years
About Akums Drugs & Pharmaceuticals Ltd.
Akums Drugs & Pharmaceuticals Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing operations, quality assurance systems, validation workflows, GMP-regulated production activities, and healthcare manufacturing services.
Key Responsibilities
Support QA validation and compliance activities.
Prepare validation protocols and operational reports.
Maintain QA records and GMP documentation.
Coordinate with production and QC teams.
Monitor validation workflows and quality systems.
Ensure adherence to SOP procedures and regulatory standards.
Prepare audit reports and compliance documentation.
Support troubleshooting and QA coordination workflows.
Participate in qualification and validation review activities.
Assist in continuous improvement of quality systems.
Required Skills
Strong knowledge of QA validation and GMP operations.
Understanding of pharmaceutical compliance workflows.
Knowledge of validation documentation and SOP systems.
Experience in audit coordination and reporting activities.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of regulatory standards and QA systems.
Ability to manage validation schedules and workflows.
Attention to compliance accuracy and documentation standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Pharma
Industry
Pharmaceutical
Why Join Akums Drugs & Pharmaceuticals Ltd.?
Akums Drugs & Pharmaceuticals Ltd. offers professionals opportunities to work in regulated pharmaceutical environments with exposure to validation systems, QA workflows, GMP operations, and pharmaceutical manufacturing activities.
How to Apply
Interested candidates can apply through ACKJOBS for this QA – Validation Executive 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.
Akums Drugs & Pharmaceuticals Ltd. is hiring professionals for the role of QA – Validation Executive for its pharmaceutical quality assurance operations located in Lalru, Punjab, India. This full-time opportunity is ideal for candidates with 2+ years of experience in QA validation operations, pharmaceutical compliance systems, validation documentation workflows, GMP procedures, audit coordination activities, quality assurance systems, SOP implementation, regulatory documentation, process validation workflows, and regulated pharmaceutical industry environments.
The selected candidate will support validation and quality assurance activities associated with pharmaceutical manufacturing systems and GMP operations. Responsibilities include preparing validation protocols and reports, maintaining QA records and GMP documentation, coordinating with production and QC teams for validation support activities, monitoring compliance workflows and quality systems, ensuring adherence to SOP procedures and regulatory standards, preparing audit reports and operational documentation, assisting in troubleshooting and QA coordination workflows, participating in validation review and compliance activities, supporting process qualification and operational improvement initiatives, and maintaining continuous improvement of pharmaceutical quality systems.
This role offers valuable exposure to pharmaceutical quality systems, GMP-regulated workflows, validation coordination activities, compliance operations, documentation systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in pharmaceutical QA and validation careers can strengthen their technical and operational expertise through this opportunity.
Location
Lalru, Punjab, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
2+ Years
About Akums Drugs & Pharmaceuticals Ltd.
Akums Drugs & Pharmaceuticals Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing operations, quality assurance systems, validation workflows, GMP-regulated production activities, and healthcare manufacturing services.
Key Responsibilities
Support QA validation and compliance activities.
Prepare validation protocols and operational reports.
Maintain QA records and GMP documentation.
Coordinate with production and QC teams.
Monitor validation workflows and quality systems.
Ensure adherence to SOP procedures and regulatory standards.
Prepare audit reports and compliance documentation.
Support troubleshooting and QA coordination workflows.
Participate in qualification and validation review activities.
Assist in continuous improvement of quality systems.
Required Skills
Strong knowledge of QA validation and GMP operations.
Understanding of pharmaceutical compliance workflows.
Knowledge of validation documentation and SOP systems.
Experience in audit coordination and reporting activities.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of regulatory standards and QA systems.
Ability to manage validation schedules and workflows.
Attention to compliance accuracy and documentation standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Pharma
Industry
Pharmaceutical
Why Join Akums Drugs & Pharmaceuticals Ltd.?
Akums Drugs & Pharmaceuticals Ltd. offers professionals opportunities to work in regulated pharmaceutical environments with exposure to validation systems, QA workflows, GMP operations, and pharmaceutical manufacturing activities.
How to Apply
Interested candidates can apply through ACKJOBS for this QA – Validation Executive 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.