Job Description
Executive – QC Validation Department | Sruzan Pharmaceuticals Pvt. Ltd. | Dehgam, Gujarat, India
Sruzan Pharmaceuticals Pvt. Ltd. is hiring professionals for the role of Executive – QC Validation for its pharmaceutical quality control and validation operations located in Dehgam, Gujarat, India. This full-time opportunity is ideal for candidates with 0 to 5 years of experience in QC validation operations, laboratory workflows, analytical testing activities, GMP compliance systems, documentation management workflows, reporting systems, and regulated pharmaceutical environments.
The selected candidate will support quality control and validation coordination activities associated with pharmaceutical manufacturing systems and analytical workflows. Responsibilities include conducting analytical testing and validation activities, maintaining quality records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring laboratory systems and validation workflows, ensuring adherence to GMP procedures and quality standards, preparing validation reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in audit review and compliance activities, supporting laboratory management systems, and maintaining continuous improvement of laboratory operations and testing efficiency.
This role offers valuable exposure to pharmaceutical laboratory systems, analytical workflows, compliance coordination activities, technical documentation systems, validation operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in pharmaceutical quality careers can strengthen their technical and operational expertise through this opportunity.
Location
Dehgam, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
0 to 5 Years
About Sruzan Pharmaceuticals Pvt. Ltd.
Sruzan Pharmaceuticals Pvt. Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, laboratory testing workflows, validation coordination activities, and healthcare product operations.
Key Responsibilities
Support QC validation and laboratory activities.
Conduct analytical testing and validation workflows.
Maintain quality records and technical documentation.
Coordinate with QA and production teams.
Monitor laboratory systems and validation activities.
Ensure adherence to GMP procedures and quality standards.
Prepare validation reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in audit review and compliance activities.
Assist in continuous improvement of laboratory systems.
Required Skills
Strong knowledge of QC validation and laboratory operations.
Understanding of analytical workflows and GMP systems.
Knowledge of validation and compliance activities.
Experience in laboratory documentation and reporting systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of SOP procedures and pharmaceutical standards.
Ability to manage laboratory schedules and workflows.
Attention to analytical accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Sc
Industry
Pharmaceutical
Why Join Sruzan Pharmaceuticals Pvt. Ltd.?
Sruzan Pharmaceuticals Pvt. Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to laboratory systems, analytical workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this Executive – QC Validation 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.
Sruzan Pharmaceuticals Pvt. Ltd. is hiring professionals for the role of Executive – QC Validation for its pharmaceutical quality control and validation operations located in Dehgam, Gujarat, India. This full-time opportunity is ideal for candidates with 0 to 5 years of experience in QC validation operations, laboratory workflows, analytical testing activities, GMP compliance systems, documentation management workflows, reporting systems, and regulated pharmaceutical environments.
The selected candidate will support quality control and validation coordination activities associated with pharmaceutical manufacturing systems and analytical workflows. Responsibilities include conducting analytical testing and validation activities, maintaining quality records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring laboratory systems and validation workflows, ensuring adherence to GMP procedures and quality standards, preparing validation reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in audit review and compliance activities, supporting laboratory management systems, and maintaining continuous improvement of laboratory operations and testing efficiency.
This role offers valuable exposure to pharmaceutical laboratory systems, analytical workflows, compliance coordination activities, technical documentation systems, validation operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in pharmaceutical quality careers can strengthen their technical and operational expertise through this opportunity.
Location
Dehgam, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
0 to 5 Years
About Sruzan Pharmaceuticals Pvt. Ltd.
Sruzan Pharmaceuticals Pvt. Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, laboratory testing workflows, validation coordination activities, and healthcare product operations.
Key Responsibilities
Support QC validation and laboratory activities.
Conduct analytical testing and validation workflows.
Maintain quality records and technical documentation.
Coordinate with QA and production teams.
Monitor laboratory systems and validation activities.
Ensure adherence to GMP procedures and quality standards.
Prepare validation reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in audit review and compliance activities.
Assist in continuous improvement of laboratory systems.
Required Skills
Strong knowledge of QC validation and laboratory operations.
Understanding of analytical workflows and GMP systems.
Knowledge of validation and compliance activities.
Experience in laboratory documentation and reporting systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of SOP procedures and pharmaceutical standards.
Ability to manage laboratory schedules and workflows.
Attention to analytical accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B.Sc
Industry
Pharmaceutical
Why Join Sruzan Pharmaceuticals Pvt. Ltd.?
Sruzan Pharmaceuticals Pvt. Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to laboratory systems, analytical workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this Executive – QC Validation 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.