Job Description

We are seeking a detail-oriented and proactive Quality Assurance Executive to join our team. The ideal candidate will be responsible for ensuring the quality and compliance of our products through the preparation and execution of various documentation related to batch processing, standard operating procedures, standard test procedures, and vendor qualifications.

Responsibilities:

Preparation of Annual Product Quality Reviews (APQRs) and Certificate of Analysis (CoAs):

Compile and analyze data to prepare APQRs and CoAs in accordance with regulatory requirements. Ensure accuracy and completeness of documentation.

Document Issuance and Control Log Book Record Updation:

Maintain a comprehensive document issuance and control log book. Update records promptly and accurately to reflect the latest documentation status.

Batch Processing Record Preparation:

Prepare batch processing records for manufacturing operations. Verify adherence to standard procedures and specifications.

Preparation and Execution of Standard Operating Procedures (SOPs):

Develop, review, and update SOPs as needed. Ensure SOPs are effectively communicated and followed across relevant departments.

Preparation of Standard Test Procedures (STPs) and Specifications:

Develop STPs and specifications for product testing. Collaborate with relevant teams to establish testing protocols.

Preparation of Dispatch Documents and Labels of Finished Products:

Generate accurate dispatch documents and labels for finished products. Verify compliance with regulatory requirements and customer specifications.

Preparation of Documents Related to Vendor Qualifications and Compliance of SOP:

Assist in the documentation related to vendor qualifications and compliance. Ensure vendors meet the necessary quality standards and requirements outlined in SOPs.

Qualifications:

Bachelor's degree in a relevant field (e.g., Chemistry, Pharmacy, Biology, or related discipline). Proven experience in quality assurance or related roles within the pharmaceutical or manufacturing industry. Strong understanding of regulatory requirements and quality standards (e.g., cGMP). Excellent attention to detail and organizational skills. Proficiency in document management and record-keeping. Ability to effectively communicate and collaborate with cross-functional teams. Prior experience with document preparation and execution in a regulated environment is preferred.

How to Apply:

Interested candidates should submit their resume, a cover letter. Please include "Quality Assurance Executive Application" in the subject line.

Job Type: Full-time

Pay: ?20,000.00 - ?30,000.00 per month

Benefits:

Provident Fund
Schedule:

Day shift
Ability to commute/relocate:

Cherlapally, Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Required)
Education:

Bachelor's (Required)
Experience:

total work: 2 years (Required)
Location:

Cherlapally, Hyderabad, Telangana (Preferred)
Work Location: In person