Vinta Laboratories Pvt. Ltd. Walk-in Interview for API Production & Quality Control Jobs
Are you searching for an exciting career opportunity in the pharmaceutical industry? Vinta Laboratories Pvt. Ltd., formerly known as Swaasa Pharma, is conducting a walk-in interview for skilled professionals in API Production and Quality Control. This guide provides all the essential details, requirements, and tips to help you prepare for the event.
Table of Contents
- Overview of Vinta Laboratories Pvt. Ltd.
- Job Openings and Roles
- API Production
- Quality Control Jobs
- Essential Qualifications and Experience Requirements
- Job Location
- Walk-In Interview Dates and Venue
- Detailed Job Descriptions
- API Production Responsibilities
- Quality Control Jobs Responsibilities
- Required Documents for the Interview
- Compensation and Benefits
- How to Apply and Register
- Interview Preparation Tips
- FAQs
Overview of Vinta Laboratories Pvt. Ltd.
Vinta Laboratories Pvt. Ltd. is a growing pharmaceutical company that specializes in producing high-quality Active Pharmaceutical Ingredients (APIs) essential for the healthcare sector. Formerly operating as Swaasa Pharma, Vinta Laboratories has a strong foundation in pharmaceutical manufacturing and is known for its commitment to excellence and innovation. The company’s facilities are located in Atchutapuram, Visakhapatnam, Andhra Pradesh, and they are hiring candidates to strengthen their API production and quality control teams.
Job Openings and Roles
Vinta Laboratories has multiple positions open for candidates experienced in API Production and Quality Control Jobs. Let’s take a closer look at these roles:
API Production
API (Active Pharmaceutical Ingredient) Production involves creating the active ingredients used in medications. This role is essential to the pharmaceutical industry, as these APIs are key components of drugs. Candidates for this position will need to have hands-on experience with reactors, centrifuges, and cleanrooms, along with strong documentation skills.
Quality Control
The Quality Control (QC) team ensures that products meet the highest quality standards before they reach consumers. This role requires experience in API quality control and the ability to handle equipment like High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). Accuracy, precision, and attention to detail are vital in this position.
Essential Qualifications and Experience Requirements
For both the API Production and Quality Control positions, candidates must meet specific educational and experience qualifications:
- Educational Qualification: B.Sc. or M.Sc. in relevant fields.
- Experience: 2-4 years of relevant work experience in the pharmaceutical industry, specifically in API production or quality control.
- Additional Requirement for API Production: Hands-on experience with reactor and centrifuge operations, as well as familiarity with cleanroom environments.
Job Location
The job location for both roles is at Atchutapuram, in the bustling Visakhapatnam district. This area is a growing industrial hub with facilities focused on manufacturing and pharmaceutical production, making it an ideal setting for professionals in the pharmaceutical field.
Walk-In Interview Dates and Venue
The walk-in interviews will be held over two days. Here’s everything you need to know:
- Dates: 1st November 2024 (Friday) & 2nd November 2024 (Saturday)
- Venue: Vinta Labs, Plot No: 23-D, APIIC, Lalam Koduru, Rambilli, Anakapalli, Visakhapatnam.
Make sure to arrive on time and be prepared with all the required documents.
Detailed Job Descriptions
API Production Responsibilities
API Production is a critical process, involving several specialized tasks:
- Operating Reactors and Centrifuges: Candidates must have hands-on experience managing reactors and centrifuge equipment. These systems are crucial in the API manufacturing process, requiring careful handling and technical knowledge.
- Maintaining Cleanroom Standards: Cleanrooms are sterile environments essential for API production, requiring strict adherence to hygiene and safety protocols.
- Documentation: Accurate and comprehensive documentation is a must in API production, including logging procedures, material usage, and any deviations. This role requires excellent record-keeping skills to meet industry standards.
- Safety Compliance: Ensuring compliance with safety regulations is crucial to prevent accidents and maintain a safe work environment.
Quality Control Responsibilities
Quality Control specialists at Vinta Laboratories are expected to:
- Operate HPLC and GC Machines: These sophisticated machines are essential for analyzing and ensuring the purity and quality of APIs.
- Conduct Rigorous Testing: QC teams are responsible for testing samples, assessing purity levels, and identifying contaminants to ensure the APIs meet regulatory standards.
- Documentation: Detailed documentation is vital in quality control. Every test, observation, and result must be recorded precisely to maintain quality assurance.
- Quality Audits and Compliance: The role requires adherence to Good Manufacturing Practices (GMP) and a thorough understanding of quality audits.
Required Documents for the Interview
To streamline the interview process, bring the following documents:
- Updated Resume
- Photocopies of Educational Certificates
- Last Three Months’ Payslips
- Last Three Months’ Bank Statements
Having these documents ready will demonstrate your preparedness and professionalism.
Compensation and Benefits
Vinta Laboratories offers an attractive benefits package to employees, including:
- Free Transportation: Employees have access to a complimentary transportation service, making it convenient to commute.
- Subsidized Canteen: Enjoy meals at a reduced cost within the company canteen.
- Employee State Insurance (ESI) & Provident Fund (PF): Financial security is assured through these statutory benefits.
- Medical Insurance: Comprehensive medical coverage is provided for the employees and their families.
- Group Term Life Insurance (GTPL): This provides added financial security in the form of life insurance.
These benefits reflect Vinta Laboratories’ commitment to supporting and taking care of its employees.
How to Apply and Register
Interested candidates can reach out to Vinta Laboratories to register for the interview:
- Mobile Contact: 9441 699 345
- Email: [email protected]
This initial contact will allow you to confirm your eligibility and make any necessary arrangements for the interview.
Interview Preparation Tips
Preparing thoroughly for the interview can increase your chances of success:
- Research Vinta Laboratories Pvt. Ltd.: Understand their history, mission, and recent developments. Knowing about the company shows that you are genuinely interested.
- Review Technical Skills: Brush up on API production or quality control techniques, especially relevant equipment like HPLC and GC.
- Organize Your Documents: Have all necessary documents ready and organized in a professional manner.
- Prepare for Common Interview Questions: Expect questions on your experience, technical skills, and problem-solving abilities in API production or QC.
- Dress Professionally and Arrive Early: Arriving early will give you time to get comfortable and shows punctuality.
Conclusion
Vinta Laboratories Pvt. Ltd.’s walk-in interview offers a promising opportunity for those with a background in API production and quality control. The positions not only offer competitive benefits but also place candidates in a leading role within the pharmaceutical industry. Whether you are an API production specialist or a QC expert, this is an excellent opportunity to join a reputable company and further your career in pharmaceuticals.
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