Ipqa Trainee

2 weeks ago


Sanand, India Scicore Nutra Pvt Ltd Full time

**Job description**

**Job** **Description** **IPQA Trainee**

Scicore Nutra Private Limited is a state-of-the-art facility, located in Sanand Gujarat, is
dedicated to producing high-quality nutrition products that are safe, effective, and meet the highest standards of quality. Our team of experts is committed to ensuring that every product we manufacture is produced with the utmost care and attention to detail.

At our manufacturing unit, we use only the best raw materials and employ advanced manufacturing processes to ensure that our products are of the highest quality. We also adhere to strict quality control measures to ensure that every product meets our rigorous standards. This starts with doing a rigorous vendor qualification as well as testing of all raw materials supplied by these vendors for every batch. We do in-house stability studies to make sure our products last the full shelf life and give the best results to our customers. Our goal is to provide our customers with nutraceutical products that promote health and wellness, and we are committed to using science-backed ingredients and formulations to achieve this goal. We are also committed to continuous innovation and improvement and are always looking for new ways to enhance our products and processes.

**Benefits** **Provided**:
1. free Air-Conditioned Transportation to the Factory
2. Paid Leave
3. Tea/Coffee & Canteen Facility
4. Accident Insurance
5. Provision for Bonus & Gratuity
6. Training programs for professional advancement
7. Progressive work environment conducive to personal and professional growth

**Job** **Title**:IPQA Trainee**
**Role & Responsibility**:

- Implementation (and, when needed, establishment) and monitoring of the cGMP compliance with cGMP requirement and quality system.
- To ensure the Preparation, Issuance, Review, Revision and Retrieval of the documents like SOPs, Formats, Log books, Batch records & Protocols, etc.
- Issuance and tracking of QMS related documents i.e. Change Control, Deviation, OOS, QRM, CAPA, Market Completion etc.
- To review Master formula record, Master batch record, Specification, MOA/STP, Worksheet etc.
- To prepare the Annual Product Quality Review (APQR) and ensure its implementation.
- Assist and participate in Qualification/Validation of the equipment system and process.
- To conduct or organize revalidation activities at the defined frequency.
- Preparation & review of Validation Master Plan and Site Master File, Validation Protocol like Process Validation, Cleaning Validation, Hold Time Validation etc.
- To perform Vendor Qualification of Raw material and Packing Material.
- To participate Investigation reports Market Complaints, Deviation, OOS etc.
- Periodic review of all quality functions and procedure for appropriateness and review of related documents.
- To perform In-process checks during Manufacturing & Packing activities.
- To perform Line Clearance activities for various area and equipment.
- To perform sampling activities at various Manufacturing and Packing stages as per SOPs, Protocols etc.
- To collect Retain Sample, Stability Sample and any other sample (If required).
- To review executed Batch Records.
- Compilation and review of the Batch records, Certificate of Analysis, etc. which are required for release of batches.
- To Perform finished product batch release as per SOPs.
- Preparation of stability protocol, Review of stability data and other stability related documentation activity.
- To review of regulatory requirements and its compliance.
- Responsible for participation in periodic internal audits in accordance with applicable SOPs.
- To Perform external service provider / out service activates audits and its documents compliance.
- Any additional job responsibilities as assigned by HOD.

**Department** Quality Assurance

**Experience**:0 to 1 year
**Employment** **Type**: Full Time, Permanent
**Education**:UG: B. Pharma in Any Specialization
PG: M. Pharma in Any Specialization

B.Sc. in Any Specialization

**Role**:IPQA Trainee

**Industry Type**:Pharmaceutical & Life Sciences

**Key skills**:OSD, Gdp, IPQA, GMP, In Process Quality Assurance, Line Management, Quality Assurance

**Job Types**: Full-time, Permanent, Fresher

Pay: ₹200,000.00 - ₹300,000.00 per month

Schedule:

- Day shift

Work Location: In person