Comed Chemicals Limited is a multi-dimensional pharmaceutical organization. Apply online for the following openings if you have requested qualifications. Latest BSc Pharma Jobs. Apply online. Latest BSc Pharma Jobs details.
Location – Rania Plant /HO Office in Vadodara
Post 1 – Executive- QA
- Candidates having minimum 2 years of experience in Pharma QMS/Documentation can apply.
- Education – B.Pharma
Post 2 – Officer / Sr. Officer Production
- Candidates having minimum 2 years of experience in OSD Tablet/Capsule plant can apply.
- Education – B.Pharma
Post 3 – Officer / Jr. Officer F&D
- Candidates having minimum 0 to 1 year of experience in OSD Tablet / Capsule plant can apply.
- Education – B.Pharm
Post 4 – Officer QC
- Candidates having minimum 1 to 2 years of experience on Wet Lab in Pharma can apply.
- Education – Bsc/Msc
Post 5 – Executive Regulatory Affairs
- Candidates having 4 to 5 years of experience in Regulatory affairs in Pharma industry can apply.
- Education – B.Pharm / M.Pharm
Post 6 – Operation manager – empty hard gelatin capsule
- Candidates having 5 years of experience as a Manager in Relevant Empty Hard Gelatin Capsule can apply.
- Education – BE/BSc
Post 7 – Sr. executive – pharma export
- Candidates having 5 to 6 years of experience in International Marketing / Export in Pharma Industry can apply.
- Education – BSc/MSc/ B.Pharm/ M.Pharm/MBA – Marketing
How to apply – Interested candidates can apply on [email protected]
Greetings, friends! We’ve curated a selection of interview questions and their corresponding answers to aid you in your interview preparations for the Latest BSc Pharma Jobs. Please take advantage of these resources to ensure a successful interview experience for the Latest BSc Pharma Jobs.
For Post 1 – Executive- QA:
Question: Can you describe your experience with Pharma Quality Management Systems (QMS) and documentation?
Answer: I have over two years of experience working in Pharma QMS and documentation. In my previous role, I was responsible for maintaining and updating QMS processes, ensuring compliance with regulatory standards, and managing documentation to support quality control and assurance efforts.
Question: How do you stay updated on the latest quality standards and regulations in the pharmaceutical industry?
Answer: Staying updated is crucial in the pharmaceutical industry. I regularly attend industry seminars, workshops, and webinars, and I’m a member of professional organizations. I also actively follow regulatory updates to ensure our quality processes align with the latest standards.
For Post 2 – Officer / Sr. Officer Production:
Question: Can you share your experience in OSD Tablet/Capsule production, including any specific roles or responsibilities you’ve had?
Answer: I have over two years of experience in OSD Tablet/Capsule production. In my previous role, I was responsible for supervising production activities, ensuring adherence to GMP, and overseeing the manufacturing process from raw material handling to packaging. I also played a role in optimizing production efficiency.
Question: How do you handle unexpected production issues or deviations to ensure product quality and timelines are maintained?
Answer: When faced with unexpected issues or deviations, I follow a structured approach. I investigate the root cause, implement corrective actions, and communicate with relevant stakeholders promptly. My goal is to minimize downtime, maintain product quality, and meet production timelines.
For Post 3 – Officer / Jr. Officer F&D:
Question: Given your limited experience, how do you plan to contribute to OSD Tablet/Capsule plant operations in your role?
Answer: While I may have limited experience, I am eager to learn and apply my knowledge to F&D processes. I will work closely with senior team members to gain practical experience, contribute ideas, and assist in various aspects of formulation and development. My goal is to quickly become a valuable member of the team.
For Post 4 – Officer QC:
Question: Can you explain your experience working in the wet lab within the pharmaceutical industry, and what types of tests and analyses have you performed?
Answer: In my previous role as an Officer QC, I had 1 to 2 years of experience working in the wet lab. I conducted a wide range of tests, including chemical and physical analyses of raw materials and finished products. These tests involved techniques such as titration, spectrophotometry, and chromatography to ensure product quality and compliance with specifications.
Question: How do you ensure accuracy and precision when conducting wet lab tests, and how do you handle out-of-specification results?
Answer: Accuracy and precision are paramount in the wet lab. I meticulously follow established testing procedures, use calibrated instruments, and maintain a controlled testing environment. In case of out-of-specification results, I initiate an investigation, perform retests if necessary, and document the process thoroughly to determine the root cause and implement corrective actions.
For Post 5 – Executive Regulatory Affairs:
Question: Can you describe your experience in regulatory affairs within the pharmaceutical industry, including any specific projects or submissions you’ve been involved in?
Answer: I have 4 to 5 years of experience in pharmaceutical regulatory affairs. During this time, I’ve been responsible for preparing and submitting regulatory dossiers, ensuring compliance with local and international regulations, and liaising with regulatory agencies. One notable project I was involved in was the successful submission and approval of a new drug application (NDA) for a key product.
Question: How do you keep up with evolving regulatory requirements and changes in the pharmaceutical industry?
Answer: Staying informed about regulatory changes is essential. I subscribe to regulatory updates, attend relevant conferences, and maintain regular communication with industry peers. Additionally, I actively participate in ongoing training and professional development programs to ensure our submissions and processes align with current regulations.
For Post 6 – Operation Manager – Empty Hard Gelatin Capsule:
Question: Can you share your experience managing operations in the production of empty hard gelatin capsules, and how have you contributed to process efficiency and quality improvement?
Answer: With 5 years of experience as an Operation Manager in the production of empty hard gelatin capsules, I have overseen various aspects of capsule manufacturing. I’ve implemented process improvements, optimized equipment utilization, and ensured strict adherence to GMP standards. By closely monitoring production processes, I have consistently improved efficiency and maintained high-quality standards.
Question: How do you handle challenges related to production scheduling, resource allocation, and meeting production targets?
Answer: Managing production challenges requires a combination of effective planning and team coordination. I develop robust production schedules, allocate resources efficiently, and maintain open communication with the production team. Regular performance monitoring allows for timely adjustments to ensure we meet our production targets while maintaining product quality.
For Post 7 – Sr. Executive – Pharma Export:
Question: Can you describe your experience in international marketing and export within the pharmaceutical industry, including any specific markets you have worked with or strategies you have employed?
Answer: I have 5 to 6 years of experience in international marketing and export within the pharmaceutical industry. During this time, I have successfully managed exports to diverse markets, including North America, Europe, and Asia. My strategies have included market research, distributor selection, and regulatory compliance to ensure product entry and growth in these regions.
Question: How do you handle challenges related to international market regulations, customs, and logistics when exporting pharmaceutical products?
Answer: Exporting pharmaceutical products requires a deep understanding of regulatory compliance and logistics. I work closely with regulatory experts to ensure all documentation and labeling meet the requirements of the target markets. Additionally, I collaborate with logistics partners to streamline the shipping process and address any customs-related challenges promptly.
