Syngene 0-3 Years Exp BSc, MSc & MTech Biotech Candidates Apply For QC Executive Job

: center;">Syngene QC Executive Job For BSc, MSc & MTech Candidates

Syngene QC Executive Job For BSc, MSc & MTech Candidates. MSc, MTech and BSc Biotechnology Job in Syngene, Bangalore. Syngene is hiring Biotechnology candidates for QC Executive 1 job.

The five possible interview questions that can be asked in the technical round for QC Executive 1 position, along with their answers are posted below:

Designation: QC Executive 1

Job Location: Bangalore

Requisition ID: 53837

Department: Quality Assurance -Biologics

About Syngene

Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.

Job Description:

• To handle the Inprocess and Finished products analysis in shifts
• To perform the analysis of Stability samples.
• To handle the calibration of QC instruments/Equipment.
• To support Method tranfer/validation activities
• To ensure the completion of trainings allotted in time and support the team lead for achieving the deliverables.
• Adhere to the SOP/IOP and perform the analytical activities.
• Adhere to the good laboratory practice and compliance.
• Ensure error free analysis and documentation.
• Co-Ordinate with external vendors for ensuring timely calibration and PM activities.
• To ensure storage chambers are maintained at set t temperature limits and take timely action in case of any excursions.
• To ensure the instrument/equipment are in calibrated state.
• Ensure the breakdowns if any are rectified in time and instrument is made up and running within shortest possible time in co-ordination with service provider.
• Ensuring all time audit readiness and preparation prior to audits.
• Ensuring completion status of action items of CAPAs triggered through observations of previous audits.
• To support any other activity allotted by the team lead.

Key Responsibilities: 

• Operating in shift and ensuring release of Inprcoess/Finished product samples within TAT and by adhering to compliance norms.
• Ensuring the calibration of instruments and handling breakdown in co ordination with vendor.
• Adhering to good laboratory and analytical procedures.

Educational Qualification: Bachelor/Master of Science / Master of Technology -Biotechnology/Bioprocess Engineering

Technical/Functional Skills: 

• Entry level Knowledge on Biologics Manufacturing and testing compliance requirements.
• Good communication
• Co-Operation with team leads.

Experience: 0-3 years of experience in Biopharma manufacturing/testing.

Behavioural Skills:

• Aggressive but assertive on task completion.
• Personal integrity and good attitude.

Equal Opportunity Employer:

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

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Here are five possible interview questions that can be asked in the technical round for QC Executive 1 position, along with their answers:

1. Can you describe your experience in handling in-process and finished product analysis in a quality control (QC) setting? How do you ensure compliance with standard operating procedures (SOPs) and good laboratory practices (GLP)?

Answer: In my previous role, I have been responsible for performing in-process and finished product analysis in a QC laboratory. To ensure compliance with SOPs and GLP, I strictly follow the documented procedures, adhere to safety protocols, and maintain accurate documentation of all analytical activities. I also participate in regular training sessions to stay updated with the latest compliance requirements and best practices in QC.

2. How do you handle calibration of QC instruments and equipment? Can you provide an example of a challenging calibration task you have encountered and how you resolved it?

Answer: Calibration of QC instruments and equipment is crucial to ensure accurate and reliable results. I have experience in performing instrument calibration according to defined schedules and protocols. In a challenging calibration task, I encountered an instrument that was showing inconsistent readings. I worked closely with the vendor’s technical support team to troubleshoot the issue, identified a faulty component, and replaced it, ensuring the instrument was recalibrated and functioning properly.

3. How do you prioritize and manage your workload to ensure timely release of in-process and finished product samples within turnaround time (TAT)? Can you give an example of a time when you had to handle a high workload and meet strict deadlines?

Answer: Prioritization and effective time management are essential to meet TAT for sample release. I assess the urgency of each task, allocate resources accordingly, and plan my work schedule. In a previous situation, I was assigned a high workload due to a sudden surge in sample volume. To meet the strict deadlines, I organized my tasks, collaborated with colleagues for support, and efficiently managed my time, ensuring all samples were analyzed and released within the required TAT.

4. What are the key compliance requirements and regulations specific to biopharma manufacturing and testing that you are familiar with? How do you stay updated with the evolving regulations in the industry?

Answer: I am familiar with key compliance requirements such as Good Manufacturing Practices (GMP) and applicable regulatory guidelines specific to biopharma manufacturing and testing. To stay updated, I regularly review industry publications, attend training sessions, and actively participate in professional forums and conferences related to biopharmaceuticals. I also engage in continuous learning to ensure compliance with evolving regulations and industry best practices.

5. Can you share an example of a time when you demonstrated assertiveness and personal integrity in completing a task? How do you maintain a positive attitude in challenging situations?

Answer: In a previous project, there was a discrepancy in the test results that required investigation. Despite facing pressure to conclude the analysis quickly, I maintained my personal integrity by following the established protocols, conducting thorough investigations, and communicating the findings honestly. I demonstrated assertiveness by raising concerns and working collaboratively with the team to rectify the issue. To maintain a positive attitude in challenging situations, I focus on problem-solving, seek support from colleagues, and maintain open and effective communication channels.

Remember to adapt your answers based on your own experiences and skills. These sample answers can serve as a reference to help you prepare for the interview.

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