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