Merck MSc Microbiology, Biotech, Biochem & Life Sciences Applications Expert, Apply Online
Merck MSc Microbiology, Biotech, Biochem & Life Sciences Applications Expert, Apply Online. Merck New Delhi Jobs. Application Senior Expert Biomonitoring jobs at Merck. Interested and eligible applicants can check out all of the details on the same below
Role: Application Senior Expert, BioMonitoring India CMAT Lab
Location: New Delhi, Delhi – India
Req ID: 262723
Reporting: Regional Marketing Manager APAC (Asia Pacific), Dotted line to India Marketing Team Lead.
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.
Responsibilities Include:
- Responsible for managing and maintaining application laboratory
- Carry out F&B Feasibility trials, Application studies, trouble shooting and Method development. Creating new F&B application data for new matrices that comes across country e.g. meat, spices, juices etc.
- Create and manages all laboratory documents, SOPs and records.
- On-site technical support with demos, method development, troubleshooting and application support whenever needed
- Plan and conduct internal and external trainings on BioMonitoring products and applications.
- Work closely with FSSAI for training for the personnel both on technology and applications on all related F&B topics.
- Collaborate with commercial team to provide effective solutions to support business objectives.
- Extend support to APAC Regional and country marketing teams in activities including seminars, training, validation, and other marketing campaigns.
- Awareness of regulatory requirements in the F&B industry including (and not exhaustive)
- ISO methods, FDA BAM etc.
Qualifications:
- Master in Microbiology, Biochemistry, Biotechnology or relevant life science field
- >5 years of work experience in laboratory experience in performing Microbiology testing, QA/QC, F&B industry preferred.
- Knowledge on laboratory management and laboratory safety aspects.
- Knowledge on regulatory guidelines of Microbiology testing.
- Ability to resolve technical problems and adapt easily to changing needs and priorities.
- Excellent communication skills and the ability to manage customers and internal stakeholders.
- Willingness to travel for business requirements.
- Independent in managing lab and business requirements.
- Proficient in MS Office apps.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
Here are some interview questions and sample answers for the role of Application Senior Expert in the BioMonitoring India CMAT Lab:
1. Can you tell us about your experience in managing and maintaining an application laboratory? Answer: In my previous role, I was responsible for managing and maintaining an application laboratory. I oversaw the day-to-day operations, ensured equipment functionality, managed inventory, and maintained a clean and organized workspace. I also implemented best practices for laboratory safety and compliance with regulatory guidelines.
2. How would you approach conducting F&B feasibility trials and application studies? Answer: When conducting F&B feasibility trials and application studies, I would start by clearly defining the objectives and parameters of the study. I would design and execute the experiments, collect and analyze data, and interpret the results. Troubleshooting and method development would be an integral part of the process to ensure accurate and reliable outcomes. Additionally, I would document the entire process to establish a knowledge base for future reference.
3. How do you ensure the creation and management of laboratory documents, SOPs, and records? Answer: To ensure the creation and management of laboratory documents, SOPs, and records, I follow a systematic approach. I review existing documents to identify gaps or areas for improvement. I collaborate with relevant stakeholders to gather input and expertise. I then draft comprehensive and clear documents, ensuring they align with regulatory requirements. Regular updates and version control are maintained to keep them current. Additionally, I implement proper document management systems to organize and secure the records.
4. How do you provide on-site technical support and application assistance when needed? Answer: When providing on-site technical support and application assistance, I prioritize effective communication and collaboration. I work closely with the team to understand the specific requirements and challenges they are facing. I assess the situation, diagnose problems, and propose solutions or troubleshooting strategies. I also provide hands-on support, including conducting demos, assisting with method development, and troubleshooting equipment or process issues.
5. Can you describe your experience in planning and conducting internal and external training? Answer: I have extensive experience in planning and conducting internal and external training. I start by identifying the training needs of the audience and designing tailored programs to address those needs. I create engaging training materials and utilize various methodologies to facilitate effective learning. During the training sessions, I encourage participation, answer questions, and provide practical examples. I also evaluate the effectiveness of the training through feedback mechanisms and make improvements as necessary.
6. How have you collaborated with regulatory bodies like FSSAI in the past? Answer: In my previous role, I collaborated with regulatory bodies such as FSSAI on multiple occasions. I established a strong working relationship by actively participating in industry conferences, workshops, and training sessions organized by FSSAI. I also engaged in regular communication to stay updated on new guidelines and regulations. Additionally, I facilitated training programs for laboratory personnel in partnership with FSSAI to ensure compliance with regulatory requirements.
ALL THE BEST!
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