Chemistry job at Jubilant as QC executive. Interested candidates can apply online now.
Job role –Â Asst. Officer / Executive / Sr. Executive- QC
Grade –Â A2 A3
Department – Quality Control
Job location –Gajraula, Uttar Pradesh
Job provider –
Jubilant Ingrevia Limited (Jubilant Life Sciences Limited) is one of India’s leading corporate and a highly treasured brand throughout the world. The organization has a presence in the fields of Pharma and Life Sciences, Agri & Performance Polymers, Food & Retail, Oil & Gas and Services.
Job Summary-
The candidate is required to have complete experience in API/Bulk/ Intermediates industries as per global regulatory requirements and be responsible for implementation & compliance of ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP / global QMS requirements at SEZ site.
About you –Â
- Knowledge about IMS systems (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP.
- Analytical skill for QC instruments, i.e. GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point etc.
- Regularize the QC activities as per cGMP requirements.
- RM, PKG, In-process and FG sampling & Analysis.
- Co-ordination with QC staff, R&D, Commercial and production for quality & dispatch related activities for on time dispatches.
- Day to day monitoring and execution online all IPQC and FG analysis activities.
- Resolve the trouble shooting related to QC activities.
- Knowledge about 21 CFR Part 211, 111 with data integrity (Part-11)
- Awareness about responsible care (Environment, Health, Safety and Security)
Qualification & Experience for the Chemistry job at Jubilant –Â
- M.Sc. (Chemistry) with 2 – 6 yrs.
- Handling, Calibration and Hand-on experience of all QC instruments.
- Compliance of 21 CFR Part-11.
- Troubleshooting related to QC analytical instrument
Apply online
We are providing some of the expected interview questions and answers for your reference for the Chemistry job at Jubilant. Please practice the same before you are going for the interview. All the best!!!!!
Question 1: Can you explain your experience in implementing and ensuring compliance with global regulatory requirements in the API/Bulk/Intermediates industries?
Answer: In my previous roles, I have worked extensively in API/Bulk/Intermediates industries and have a solid understanding of global regulatory requirements. I have hands-on experience in implementing and ensuring compliance with standards such as ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP, and other global QMS requirements. I have successfully led teams and implemented processes that align with these regulatory frameworks to maintain high-quality standards in manufacturing and quality control operations.
Question 2: How would you ensure regularized QC activities as per cGMP requirements?
Answer: To ensure regularized QC activities as per cGMP requirements, I would start by establishing clear standard operating procedures (SOPs) that outline the specific protocols and guidelines for quality control processes. I would implement robust documentation systems to record and track QC activities consistently. Additionally, I would conduct periodic audits and inspections to verify compliance, identify any gaps, and implement corrective actions as necessary. Regular training and awareness programs for QC staff would also be conducted to ensure adherence to cGMP requirements.
Question 3: Could you share an example of a situation where you successfully coordinated with different departments to ensure quality and timely dispatches?
Answer: In a previous role, I was responsible for coordinating quality and dispatch-related activities between the QC, R&D, commercial, and production departments. One particular instance stands out where we had a tight deadline for dispatching a batch of finished goods. I proactively initiated meetings with each department to align on the priorities and timelines. I ensured that the QC analysis was completed efficiently and accurately, communicated the results to the production team promptly, and worked closely with the commercial team to expedite the necessary documentation and logistics. Through effective coordination and communication, we were able to meet the dispatch deadline without compromising on quality.
Question 4: How would you handle troubleshooting related to QC activities?
Answer: When faced with troubleshooting related to QC activities, I would follow a systematic approach. First, I would carefully analyze the issue to identify the root cause, using my analytical skills and knowledge of QC instruments. I would consult relevant resources such as instrument manuals, scientific literature, or expert colleagues, if necessary. Once the root cause is determined, I would develop and implement appropriate corrective actions to resolve the issue. It’s important to document the troubleshooting process and communicate the findings and solutions to the relevant stakeholders to prevent future occurrences.
Question 5: How do you ensure compliance with 21 CFR Part 211, 111 with data integrity (Part-11)?
Answer: Compliance with 21 CFR Part 211 and 111, along with data integrity (Part-11), requires a comprehensive approach. Firstly, I would ensure that all relevant personnel receive proper training on the regulations and their implications for our operations. I would establish robust documentation practices, including electronic data management systems with appropriate access controls and audit trails. Regular audits and self-inspections would be conducted to assess compliance, identify potential gaps, and implement corrective actions. Additionally, I would stay updated with regulatory changes and collaborate with cross-functional teams to implement necessary updates to maintain compliance
