Bpharm job as Quality officer at Apotex. Qualified and interested candidates can apply now.
Job position – Senior Officer, Quality
Job posting – Bangalore
Job Summary –
Perform and report the analysis of In-Process samples, finished products, Stability samples and Cleaning Validation.
Job Responsibilities –
- To ensure timely completion of analysis and data completion for the same.
- To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems.
- To perform the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples and Cleaning validation.
- To Prepare Stability Trend Reports for Laboratory samples.
- To collect and maintain various laboratory samples.
- To generate and maintain records related to laboratory samples.
- Works as a member of a team to achieve all outcomes.
- Performs all work in accordance with all established regulatory and compliance and safety requirements.
- Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
- To assist the Senior Analyst / Team Leader/Group Leader in the day-to-day functioning of the Quality Control Laboratory.
- Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
- All other duties as assigned.
Job Requirements for Bpharm job as Quality officer –
- M.Sc\BPham or any equivalent degree
- Knowledge, Skills and Abilities
- Effective command over verbal and written communication with good interpersonal skills.
- Command on Microsoft Office (Word, Excel).
- Able to prioritize the tasks.
- Best in effective planning of work activities to meet timelines.
- Experience – Minimum 2 to 4 years of experience in GMP regulated pharmaceutical industry.
Hello there, Attaching some of the expected interview questions and answers here. Prepare well for the interview for the Bpharm job as Quality officer. Good luck!!!
Can you explain your experience in performing analysis of in-process samples, finished products, stability samples, and cleaning validation?
Answer: In my previous role at XYZ Pharmaceuticals, I was responsible for performing analysis of various samples including in-process samples, finished products, stability samples, and cleaning validation. I have hands-on experience in conducting tests, utilizing analytical instruments, and interpreting the results accurately. I ensured timely completion of analysis and maintained detailed documentation of the analysis and results. I am familiar with cGLP (current Good Laboratory Practices) and adhered to all regulatory requirements while performing the analyses.
How have you demonstrated effective planning and prioritization skills in your previous role?
Answer: In my previous role, I consistently demonstrated effective planning and prioritization skills to meet tight deadlines and ensure timely completion of tasks. I utilized tools such as project management software, calendars, and to-do lists to organize my work activities. By carefully assessing the urgency and importance of each task, I allocated my time and resources efficiently. I also communicated with team members and stakeholders to align priorities and avoid any bottlenecks in the workflow.
Could you explain your experience in generating stability trend reports for laboratory samples?
Answer: During my tenure at ABC Pharmaceuticals, I was responsible for generating stability trend reports for laboratory samples. I collected and analyzed data from stability studies, identified trends, and prepared comprehensive reports to monitor the stability of products over time. I utilized statistical techniques and graphical representations to present the data effectively. Additionally, I collaborated with cross-functional teams to ensure the accuracy and reliability of the stability trend reports.
How have you ensured compliance with regulatory requirements and quality systems in your previous role?
Answer: Compliance with regulatory requirements and adherence to quality systems are of utmost importance in the pharmaceutical industry. In my previous role, I ensured compliance by strictly following cGLP guidelines and maintaining accurate documentation throughout the testing and analysis process. I actively participated in internal and external audits to demonstrate our adherence to regulatory standards. I also proactively updated myself with the latest regulatory guidelines and implemented necessary changes in our quality systems to stay compliant.
What is your experience working in a team-oriented environment and how have you contributed to team success?
Answer: I have extensive experience working in team-oriented environments and understand the value of collaboration. In my previous role, I actively participated in cross-functional teams, contributing my expertise in quality control to achieve team goals. I effectively communicated with team members, listened to their perspectives, and offered my insights to solve problems and make informed decisions. I believe in fostering a positive and supportive team culture where everyone feels valued and motivated to contribute their best.
