Tata Chemicals Hiring MSc Chemistry For Quality Control
Tata Chemicals Hiring MSc Chemistry for the position of Team Member – Quality Control in Nellore, India. Interested applicants can check out the details below and Apply Online
Job title: Team Member – Quality Control
Job Location: Nellore, India
Job Category: Quality Control
Job Type: Full Time
Education: M.Sc. in Chemistry
Job Description
Job Role & Responsibilities:
- Develop methods and perform method validations. Strong experience in HPLC, IC, AAS, UV.KF, Water activity, SOR and other conventional test methods.
- Perform analytical procedures on raw materials, in-process samples and finished products as per SOPs.
- Maintenance of record of all testing results in timely manner and perform computations leading to accurate data reporting.
- To help in maintenance of laboratory supplies including chemicals, equipment and equipment parts.
- Adherence to plant and laboratory GMP’s and safety guideline to maintain a clean and safe work area at all times.
Functional Competencies:
- Lab Testing Procedures & Analytical Skills
- Expertise in LIMS
- Quality Management System
Desirable Attributes:
- SAP Working knowledge
- Excellent Communication skills
Qualification, Experience and industry: M.Sc. in Chemistry with 6 to 7 years of experience in relevant field preferably from food, dairy, nutrition, nutraceutical and pharma industry
. Understanding of USFDA, EPA, USDA, Kosher Codex Ehedg, 3A will be an added advantage.
Here are Possible interview questions and answers based on the job application provided:
1. Question: Can you describe your experience with developing methods and performing method validations in quality control?
Answer: In my previous role, I was responsible for developing methods and performing method validations in quality control. I have strong experience in various analytical techniques such as HPLC, IC, AAS, UV, KF, Water activity, and SOR. I have successfully developed and validated methods to ensure accurate and reliable testing of raw materials, in-process samples, and finished products. I am familiar with following SOPs and documenting all testing results in a timely manner to maintain accurate data reporting.
2. Question: How do you ensure adherence to Good Manufacturing Practices (GMPs) and safety guidelines in a laboratory setting?
Answer: Adherence to GMPs and safety guidelines is crucial in maintaining a clean and safe work area. I prioritize adherence to these guidelines by strictly following established protocols and procedures. I ensure proper storage and handling of chemicals, regular maintenance of equipment, and maintaining a clean and organized laboratory environment. Additionally, I actively participate in safety training programs and encourage a culture of safety among team members to minimize risks and maintain a safe working environment.
3. Question: Can you provide an example of a situation where you utilized your analytical skills and expertise in LIMS (Laboratory Information Management System)?
Answer: In my previous role, I encountered a complex analytical challenge involving multiple samples and parameters. I effectively utilized my analytical skills and expertise in LIMS to streamline the testing process. By leveraging the capabilities of the LIMS, I optimized the sample tracking, data management, and reporting workflow. This resulted in improved efficiency, enhanced data accuracy, and quicker turnaround time for test results, ultimately contributing to overall productivity and customer satisfaction.
4. Question: How have you contributed to maintaining and managing laboratory supplies, including chemicals and equipment?
Answer: As part of my role, I have actively contributed to maintaining and managing laboratory supplies. I have experience in inventory management, ensuring an adequate supply of chemicals, reagents, and consumables. I have also coordinated with vendors to procure necessary equipment and equipment parts. By implementing efficient tracking systems and maintaining detailed records, I have successfully optimized supply levels, reducing downtime and ensuring smooth laboratory operations.
5. Question: How do you stay updated with industry regulations and quality management systems?
Answer: Staying updated with industry regulations and quality management systems is essential in the field of quality control. I regularly engage in professional development activities, such as attending seminars, webinars, and conferences, to stay abreast of industry trends and regulatory changes. I also actively participate in internal and external training programs to enhance my knowledge and understanding of quality management systems. By staying updated, I can effectively apply best practices and ensure compliance with relevant standards and regulations.
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