Assistant Manager (QA) at Jubilant Generics Limited in Roorkee, Uttarakhand Jubilant Generics L[...]

Sidculindustries; Haridwar; On-site; INR 700,000 - 900,000; Full time

Job summary

A pharmaceutical company is seeking an Assistant Manager – QA to oversee quality assurance processes. The role requires 4+ years of experience and graduate qualifications. Responsibilities include managing market complaints, quality metrics, and compliance with cGMP requirements. Ideal candidates will have strong communication skills and a proactive approach to quality management. This position is full-time in Roorkee, Uttarakhand.

Qualifications

• 4+ years of relevant experience in quality assurance.
• Ability to coordinate and log quality-related activities.
• Excellent communication and interpersonal skills.

Responsibilities

• Act as complaint coordinator for market complaint management.
• Compile Quality Metric in coordination with other departments.
• Initiate and log Management Notification related to quality events.
• Prepare, track and log Field alert reports and customer notifications.
• Track and log product recall activities.
• Log and investigate temperature excursions.
• Prepare and review departmental SOPs for cGMP compliance.
• Coordinate approvals for change controls and validations.

Skills

Excellent communication

Inter-personal skills

Quality metrics

Education

Graduate

Job description

Assistant Manager – QA at Jubilant Generics Limited in Roorkee, Uttarakhand

Job Title: Assistant Manager – QA

Location: Roorkee, Uttarakhand, India

Position Type: Full-time

Salary: As per the company standards

Experience: 4+ years

Education: Graduate

Responsibilities of Assistant Manager – QA

• Act as complaint coordinator for market complaint acknowledgement, logging, investigation, response preparation, response sharing & closing.
• Compile Quality Metric in coordination with other departments.
• Initiate and log Management Notification related to quality events.
• Prepare, track and log Field alert reports and customer notifications.
• Track and log product recall activities.
• Log and investigate temperature excursions in coordination with Supply Chain.
• Prepare and review departmental SOPs to meet cGMP requirements.
• Coordinate approvals for change controls, deviations, process validation & stability protocols.

The successful candidate will possess excellent communication & inter-personal skills.

If you have relevant experience and are interested in this opportunity, please apply at the below link.

About Jubilant Generics Limited

Jubilant Generics Limited is a subsidiary of Jubilant Pharma focused on the development, manufacturing and distribution of generic pharmaceutical products and dosage forms from its Roorkee facility in Uttarakhand. The company’s operations support global markets with quality‑compliant medicines across various therapeutic areas.