◾ Amneal Pharmaceutical announcement for walk in interview on 23rd February 2025 for multiple position in pharmaceutical sector. Amneal Pharmaceutical conducted walking interview on various position in Manufacturing -Production and packing Department at Sanand, Ahmedabad location.
◾ Here’s a section with interview Answers and Questions that we can added in this blog post to help candidate prepare for interview at Amneal Pharmaceutical or any other company.
Amneal Pharmaceutical Job Opportunity 2025
| Table Of Contents |
|---|
| 1. Company Profile |
| 2. Vacancy Details |
| 3. Walk-In interview Details |
| 4. Mandatory Documents |
| 5. Interview Question & Answer |
| 6. Important Link |
1. Amneal Pharmaceutical Company Profile :
◾ Amneal Pharmaceuticals is a dynamic and growing company, providing a wide range of opportunities for employees in the pharmaceutical industry. Here’s an overview of the company profile specifically geared towards prospective or current employees:
◾ Company Overview
- Founded: 2002
- Founders: Chirag Patel and Chintu Patel
- Headquarters: Bridgewater, New Jersey, USA
- Industry: Pharmaceutical (Generics and Specialty Products)
- Employees: Amneal employs thousands of professionals across its manufacturing facilities, commercial operations, and research and development teams.
◾ Work Culture
Amneal fosters a collaborative, dynamic, and results-driven work culture. Employees are encouraged to innovate and contribute to the development of high-quality, affordable medications that improve the health of patients worldwide.
◾ Career Opportunities
Amneal offers a variety of roles, including:
- Research and Development (R&D): Opportunities in the formulation, development, and testing of both generic and specialty products.
- Manufacturing and Quality Control: Working in production and ensuring the high standards of product quality.
- Regulatory Affairs: Focused on ensuring compliance with governmental regulations.
- Sales and Marketing: Promoting the company’s generics and specialty products in the pharmaceutical market.
- Corporate Functions: Including HR, finance, IT, and legal support.
2. Amneal Pharmaceutical Vacancy Details :
| Designations : Operators, Officers, Executives |
| Departments : Injectables Manufacturing (Production & Packing) |
| Educational Qualifications : B.Sc, M.Sc, B.Pharm, M.Pharm, B.E, ITI, Diploma |
| Experience : 02 to 07 years in relevant fields |
| Required Skills : Candidate Must Have Hand On Experience in 1. Sterile/parenteral/aseptic, 2. Filling, sealing, filtration, production QMS, 3. Batch manufacturing, 4. Autoclave, 5. Terminal sterilization, 6. Packing, and Visual inspection 1. Line : Ophthalmic, vial, PFS, LYO, cartridges, and bag. 2. Machine Exposure : Filling machines (Groninger/Optima), Dyno Truking filling and sealing machines, Bosch filling machines, and steam sterilizers (Fedegree). |
3. Amneal Pharmaceutical Walk-In interview Details :
◾ Interview Date : 23, February 2025 (Sunday)
◾ Interview Time : 9:00 AM to 2:00 PM
◾ Interview Venue : Amneal Pharmaceuticals Pvt. Ltd, Plot No :161/1, Sanand Bavla Highway Road, Village: Pipan, Sanand, Ahmedabad – 382110
Or
◾ Interested candidate who are unable to attend interview, can share their CV on below mentioned Email id with subject line ” Application for INJManufacturing/Packing” or can apply online by screening the QR Coad :
◾ Email Id : ajaykumar,panday@amneal.com
◾ Disclaimer : Beware of fake job offers claiming to be from Amneal Pharmaceuticals Pvt. Ltd. or Companies under Amneal Group (collectively referred to as “AMNEAL”). Amneal neither send job offers from free email services like Gmail, Rediffmail, Yahoo mail, Hotmail, etc, nor charges any fees/security deposit from any job seekers. Amneal will not be responsible to anyone acting on an employment offer not directly made by Amneal. Stay vigilant and report any suspicious activity to Amneal.
4. Mandatory Documents :
◾ Candidates to attend the personal interview along with their :
- Updated CV
- Experience Certificates
- Payslip last 3 month
- Supporting documents for their Education
5. Interview Question & Answer :
1. Tell us about yourself and your experience in pharmaceuticals or manufacturing.
Answer: I have over X years of experience in the pharmaceutical manufacturing industry, specializing in the production and packaging of injectable products. I have worked extensively in sterile manufacturing environments, ensuring adherence to GMP guidelines and maintaining product quality throughout the production process. My role as an operator involved handling equipment, performing routine maintenance, and ensuring that every batch was produced within the prescribed parameters. Over time, I have advanced to roles with more responsibility, where I supervised operations, ensured compliance with regulatory standards, and led teams to improve efficiency and productivity.
2. Why are you interested in working at Amneal Pharmaceuticals?
Answer: I’ve always admired Amneal Pharmaceuticals for its commitment to producing high-quality and affordable medicines. I’m particularly excited about the opportunity to contribute to the production of injectables, a highly regulated and complex sector of pharmaceuticals. I appreciate that Amneal values innovation, quality, and patient safety. The company’s growth, both in the generic and specialty pharmaceutical space, aligns with my desire to work in a dynamic and expanding company, and I believe my skills and experience would be a great fit here.
3. What motivates you to work in the injectables manufacturing industry?
Answer: My motivation comes from the impact injectable products have on patients’ lives. The precision required in producing injectable medications, particularly in sterile environments, is something I find challenging and rewarding. It requires both attention to detail and a strict adherence to safety protocols, and I’m passionate about ensuring that these medications reach patients with the highest possible quality. I enjoy the technical and quality-driven aspects of the industry, and I am committed to improving processes and achieving production goals while maintaining strict compliance.
4. Can you explain the process of aseptic filling in injectable manufacturing? Why is it important to maintain sterility?
Answer: Aseptic filling is the process of filling sterile containers with injectable drugs in a sterile environment, preventing contamination from microorganisms. The process includes sterilizing the drug product, equipment, and containers, followed by filling under controlled conditions. It’s important to maintain sterility because even small amounts of contamination can have serious health consequences for patients, especially with injectable drugs that are directly introduced into the bloodstream. Ensuring aseptic conditions is vital to patient safety, regulatory compliance, and maintaining the company’s reputation.
5. How do you ensure that there is no contamination in the manufacturing process?
Answer: To prevent contamination, I follow strict protocols that are set out in the GMP guidelines. This includes ensuring that the sterile environment is maintained, equipment is regularly sanitized, and employees use appropriate protective gear such as gloves, gowns, and masks. I also regularly monitor and document environmental conditions such as temperature, humidity, and air quality, and perform routine checks to ensure that there are no deviations from the standard operating procedures (SOPs). Additionally, I ensure that proper training is provided to all team members so that they fully understand the importance of contamination prevention.
6. What experience do you have with equipment like Groninger, Optima filling machines, and Bosch machines?
Answer: I have hands-on experience operating and troubleshooting machines such as Groninger and Optima filling machines, as well as Bosch filling machines in injectable production lines. I am familiar with the operating procedures for these machines, including setting up, calibrating, and maintaining them to ensure optimal performance. I’ve also been responsible for monitoring the machines during production runs to identify any potential issues and resolving them quickly to minimize downtime. Regular maintenance, cleaning, and ensuring the machines are sterilized correctly are also part of my responsibilities.
7. How do you ensure compliance with regulatory standards like FDA, EMA, or other local regulations?
Answer: Compliance with regulatory standards is a top priority. I make sure that all procedures, from raw material receipt to final product packaging, strictly follow GMP guidelines and regulatory requirements set by bodies such as the FDA and EMA. I ensure proper documentation, including batch records, equipment logs, and quality control checks, to verify compliance. Regular audits are a key part of the process, and I actively participate in these audits to ensure everything is in order. Any deviations or issues are immediately flagged, and corrective actions are taken to address them.
8. How would you handle a situation where a batch is non-compliant with quality standards?
Answer: If a batch is found to be non-compliant, the first step is to halt production immediately to prevent further affected batches. I would then conduct a thorough investigation to determine the root cause of the non-compliance, whether it’s equipment malfunction, human error, or raw material quality. Once the issue is identified, corrective actions are implemented, such as recalibrating equipment or re-training staff. The batch would then undergo a comprehensive review to ensure the issue has been addressed before any release. I would also document the situation in detail to ensure that it complies with regulatory reporting requirements and prevent recurrence.
9. Describe a time when you had to work in a team to meet a production goal. How did you contribute?
Answer: At my previous company, we were tasked with increasing production efficiency while maintaining product quality during a peak period. I worked closely with the team to ensure that each phase of production ran smoothly. I took responsibility for overseeing the training of new operators on equipment, identifying areas where we could improve speed without compromising quality, and facilitating communication between departments to resolve any issues promptly. My contributions helped us meet the production goal without sacrificing quality, and we were able to increase our output by 15% without any quality failures.
10. How do you stay updated with the latest trends and technologies in the pharmaceutical manufacturing field?
Answer: I regularly attend industry webinars and conferences to stay updated on the latest trends and technological advances in the pharmaceutical manufacturing sector. I also follow publications like the International Journal of Pharmaceutics and subscribe to updates from regulatory bodies like the FDA and EMA. Additionally, I take online courses to enhance my technical knowledge, particularly in areas like process validation, new manufacturing technologies, and regulatory compliance. I also collaborate with colleagues and industry peers to exchange insights and share best practices.
6. Important Link :
| Latest Job 2025 | Click Here |
| Join Our WhatsApp Group | Click Here |