Job Description
QC Stability Analyst – QC Department | Avenza Pharmaceuticals Pvt. Ltd. | Vadodara, Gujarat, India
Avenza Pharmaceuticals Pvt. Ltd. is hiring professionals for the role of QC Stability Analyst for its pharmaceutical quality control operations located in Vadodara, Gujarat, India. This full-time opportunity is ideal for candidates with 3 to 5 years of experience in QC stability operations, analytical testing workflows, laboratory coordination activities, stability study systems, documentation management workflows, GMP compliance operations, reporting systems, and regulated pharmaceutical environments.
The selected candidate will support quality control and stability coordination activities associated with pharmaceutical manufacturing systems and laboratory workflows. Responsibilities include conducting stability analysis and QC testing activities, maintaining laboratory records and technical documentation, coordinating with QC and production teams for operational support activities, monitoring analytical workflows and stability systems, ensuring adherence to SOP procedures and laboratory standards, preparing analytical reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in stability review and compliance activities, supporting laboratory management systems, and maintaining continuous improvement of analytical operations and quality efficiency.
This role offers valuable exposure to pharmaceutical QC systems, analytical workflows, laboratory coordination activities, technical documentation systems, stability operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in quality control and analytical careers can strengthen their technical and operational expertise through this opportunity.
Location
Vadodara, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
3 to 5 Years
About Avenza Pharmaceuticals Pvt. Ltd.
Avenza Pharmaceuticals Pvt. Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, quality control workflows, analytical coordination activities, and healthcare product operations.
Key Responsibilities
Support QC stability and analytical activities.
Conduct stability testing and laboratory workflows.
Maintain laboratory records and technical documentation.
Coordinate with QC and production teams.
Monitor analytical systems and stability activities.
Ensure adherence to SOP procedures and laboratory standards.
Prepare analytical reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in stability review and compliance activities.
Assist in continuous improvement of QC systems.
Required Skills
Strong knowledge of QC stability and analytical operations.
Understanding of laboratory workflows and GMP systems.
Knowledge of analytical testing and documentation activities.
Experience in QC reporting and compliance systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of HPLC, stability studies, and SOP systems.
Ability to manage laboratory schedules and workflows.
Attention to analytical accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc / B.Pharm / M.Pharm
Industry
Pharmaceutical
Why Join Avenza Pharmaceuticals Pvt. Ltd.?
Avenza Pharmaceuticals Pvt. Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to QC systems, analytical workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this QC Stability Analyst 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.
Avenza Pharmaceuticals Pvt. Ltd. is hiring professionals for the role of QC Stability Analyst for its pharmaceutical quality control operations located in Vadodara, Gujarat, India. This full-time opportunity is ideal for candidates with 3 to 5 years of experience in QC stability operations, analytical testing workflows, laboratory coordination activities, stability study systems, documentation management workflows, GMP compliance operations, reporting systems, and regulated pharmaceutical environments.
The selected candidate will support quality control and stability coordination activities associated with pharmaceutical manufacturing systems and laboratory workflows. Responsibilities include conducting stability analysis and QC testing activities, maintaining laboratory records and technical documentation, coordinating with QC and production teams for operational support activities, monitoring analytical workflows and stability systems, ensuring adherence to SOP procedures and laboratory standards, preparing analytical reports and operational documentation, assisting in troubleshooting and QC coordination workflows, participating in stability review and compliance activities, supporting laboratory management systems, and maintaining continuous improvement of analytical operations and quality efficiency.
This role offers valuable exposure to pharmaceutical QC systems, analytical workflows, laboratory coordination activities, technical documentation systems, stability operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in quality control and analytical careers can strengthen their technical and operational expertise through this opportunity.
Location
Vadodara, Gujarat, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
3 to 5 Years
About Avenza Pharmaceuticals Pvt. Ltd.
Avenza Pharmaceuticals Pvt. Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, quality control workflows, analytical coordination activities, and healthcare product operations.
Key Responsibilities
Support QC stability and analytical activities.
Conduct stability testing and laboratory workflows.
Maintain laboratory records and technical documentation.
Coordinate with QC and production teams.
Monitor analytical systems and stability activities.
Ensure adherence to SOP procedures and laboratory standards.
Prepare analytical reports and operational documentation.
Support troubleshooting and QC coordination workflows.
Participate in stability review and compliance activities.
Assist in continuous improvement of QC systems.
Required Skills
Strong knowledge of QC stability and analytical operations.
Understanding of laboratory workflows and GMP systems.
Knowledge of analytical testing and documentation activities.
Experience in QC reporting and compliance systems.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of HPLC, stability studies, and SOP systems.
Ability to manage laboratory schedules and workflows.
Attention to analytical accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc / B.Pharm / M.Pharm
Industry
Pharmaceutical
Why Join Avenza Pharmaceuticals Pvt. Ltd.?
Avenza Pharmaceuticals Pvt. Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to QC systems, analytical workflows, operational coordination activities, and healthcare manufacturing operations.
How to Apply
Interested candidates can apply through ACKJOBS for this QC Stability Analyst 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.