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**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 with pellets pharmaceutical 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**:
Pay: ₹20,000.00 - ₹30,000.00 per month
**Benefits**:
- Provident Fund
Ability to commute/relocate:
- Cherlapally, Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Bachelor's (required)
**Experience**:
- pellets pharma company: 2 years (required)
**Location**:
- Cherlapally, Hyderabad, Telangana (preferred)
Work Location: In person