Latest Chemistry job @ Jubilant This exciting opportunity is open to candidates with B.Tech/Diploma qualifications in Chemical Engineering, and it offers a chance to be a part of a leading organization known for its commitment to innovation, quality, and excellence in the chemical sector.
Job Title: Chemist-Production
Company: Jubilant Pharmova Limited
Education Qualification for Latest Chemistry job at Jubilant: Degree in Science / Graduate Engineers -Chemical/Diploma in Chemical Engineering (Chemistry/Chemical/PCM/Bio-Chemistry)
Experience: 1 to 5 Years of relevant experience from API industry only
Key Responsibilities Include:
- Intermediate/Clean room/SRP:
- Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents.
- To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents.
- Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected.
- To ensure that the respective equipment is calibrated
- Maintaining the respective equipment /Area in clean condition.
- Online updating of equipment status boards w.r.t to equipment status.
- Identifying /Labeling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated places.
- Identify the abnormalities associated with risk and objectives by cross verifying the interlocks in equipment.
- To ensure the availability of utilities and to maintain the same by requesting the utility department whenever required.
- Material Handling:
- Receiving the raw material from the stores and storage of raw materials in the designated place
- Identification and storage of intermediates/ API’s in the designated place.
- Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected.
- To maintain the accessories per respective SOP.
- To indent, receive and issue the required documents within the timeline according to pre-approved instructions.
- To ensure that documents are being recorded contemporaneously.
- To ensure the records are updating contemporaneously and to facilitate the required documents.
- To ensure the availability of calibration documents where ever required.
- To ensure that those documents are completed and signed.
- To ensure the online entries of status board, log books and daily updating documents.
- To ensure the accessories are properly maintained/ destructed as per the respective SOP and it is properly documented.
- To submit the completed documents within the timeline as per respective SOP
Possible Interview Q & A:
1. Question: Can you describe your experience with producing intermediates, APIs, and solvent recovery according to pre-approved instructions? How do you ensure accuracy and compliance with instructions?
Answer: In my previous role, I was responsible for producing intermediates and APIs by meticulously following pre-approved instructions. I ensured accuracy by double-checking measurements, verifying process parameters, and conducting frequent quality checks. Compliance with instructions was maintained through strict adherence to Standard Operating Procedures (SOPs) and by documenting each step of the production process in Batch Production Records (BPRs). This documentation not only ensured compliance but also facilitated traceability and troubleshooting when necessary.
2.Question: How do you ensure the cleanliness and disinfection of the intermediate/pharma/SRP and equipment? Can you provide an example of a cleaning procedure you’ve followed?
Answer: Maintaining cleanliness and proper disinfection is crucial in pharmaceutical production. I have experience in cleaning procedures where I followed established protocols, used appropriate cleaning agents, and documented the cleaning process in Batch Cleaning Records (BCRs). Regular inspections and swab testing were performed to confirm the effectiveness of cleaning. Additionally, I ensured that all cleaning activities were conducted in compliance with Good Manufacturing Practices (GMP) to maintain the highest level of cleanliness and hygiene.
3. Question: Can you explain your approach to equipment calibration and its importance in the production process?
Answer: Equipment calibration is essential to ensure accuracy and consistency in the production process. I have experience in monitoring equipment calibration schedules and working closely with the maintenance and engineering teams to ensure that equipment is calibrated as per the defined procedures and timelines. Regular calibration not only guarantees the reliability of equipment but also helps in meeting quality and compliance requirements. It’s a critical aspect of maintaining production consistency and product quality.
4. Question: How do you handle material handling and storage of raw materials and intermediates? What measures do you take to maintain the storage area?
Answer: Material handling involves a systematic approach to receiving, storing, and handling raw materials and intermediates. I have experience in receiving raw materials from the stores, verifying their quality and quantity, and ensuring their proper storage in designated areas. I follow the principles of First-In-First-Out (FIFO) to prevent material expiry and contamination. Regular inspections and cleaning of the storage areas, along with documentation in accordance with SOPs, are essential to maintain the storage area’s cleanliness and organization.
5. Question: Describe your approach to documentation in a pharmaceutical production setting. How do you ensure accuracy, contemporaneous recording, and timely submission of documents?
Answer: Documentation is a critical aspect of pharmaceutical production. I prioritize accurate and contemporaneous recording by immediately documenting each step of the production process as it occurs. I also cross-check entries for consistency and completeness. To ensure timely submission, I follow a well-defined document management system, including tracking deadlines and using electronic documentation tools where available. Compliance with document completion and signatures is strictly adhered to, in line with established SOPs. This approach ensures that all documents, including batch records, logs, and status boards, are up-to-date and submitted within the required timelines.
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