Jamp Pharma Hiring-QA Position

JAMP Pharma; Ahmedabad District; On-site; INR 500,000 - 800,000; Full time

Job summary

JAMP Pharma is seeking a Quality Assurance Executive/Senior Executive to oversee the stability documentation of drugs and health products in Ahmedabad. The ideal candidate should have 3-6 years of experience in a similar role and relevant qualifications.

Responsibilities include reviewing stability data, evaluating change requests, and ensuring compliance with Good Manufacturing Practices (GMP). Interested applicants can send their profiles to [e-mail].

Qualifications

• 3-6 years of experience in Quality Assurance or related field.
• Strong understanding of stability studies and regulatory compliance.
• Ability to collaborate across departments.

Responsibilities

• Review documents related to stability of drugs and health products.
• Evaluate change control requests and their impact on stability.
• Issue recommendations based on stability data.
• Prepare stability protocols and annual reviews.
• Investigate OOS results and write non-conformity reports.
• Follow up on stability programs by third parties.
• Support other compliance areas as needed.
• Promote Good Manufacturing Practices (GMP).

Skills

Good Manufacturing Practices (GMP)

Document Management

Stability Data Analysis

Change Control Evaluation

Education

B. Pharma / M. Pharma / B.Sc / M.Sc

Job description

Dept: Quality Assurance – Stability

Position: Executive / Senior Executive

Experience: 3 – 6 years

Qualification: B. Pharma / M. Pharma / B.Sc / M.Sc

Location: Ahmedabad

Key Responsibilities:

Review and keep all the documents related to the stability of the drugs (DIN) and natural health products (NHP) on file.

Evaluate the change control requests and the impact on the stability of the products.

Review the stability data of the products and issue recommendations for the shelf life.

Prepare the stability protocols and annual stability summary review for finished products (DIN and NHP).

Review the stability results provided by the laboratories (certificates of analysis) against the product specification, investigate OOS results and write non-conformity reports.

Quarterly follow-up on ongoing stability programs made by third parties.

Keeps updated the schedule of all stability-related activities and the shelf-life information of the products.

Provides support to other compliance areas such as SOP-related activities, training, APQR and EIRA assessment, recalls, and internal audits, if needed.

Collaborates with the various activity sectors external to Quality Assurance such as the quality control analysis laboratory, product launch teams, business development, technology transfers and regulatory affairs as needed.

Promotes Good Manufacturing Practices (GMP).

Send profile at [e-mail]