Ipca Laboratories Pharma Freshers Job Vacancy – Apply Online
Dont forget to check out possible interview questions for this job below
Ipca Laboratories Ltd Kandla Gandhidham Kutch Gujarat. B Pharma and M Pharma job opening 2023,hiring freshers candidates. Freshers job opening 2023, pharma freshers job opening 2023, Candidates with bachelor’s or master’s degree in pharma may apply for the fresher’s job opening at Ipca Laboratories.
Location: Kandla Gandhidham Kutch Gujarat
Eligbility Criteria – BSC/ B pharma, M Pharma
Experience– 0 5 to 06 Year
Job Title- Quality assurance Sr. Officer
Job Description:Â
- Good knowledge of QMS Activity.
- Good knowledge of CCP.
- Good knowledge of C&P.
- Good knowledge of Validation activity.
- Â Good knowledge of Risk Assessment.
Salary:
As per Company policy
Kindly below detail mention-
Current CTC –
Expected CTC-
Notice Period –
How To Apply:
Interested Condidate kindly share with me your updated resume as per mention Mail id.
A consumer-led global pharmaceutical company, creating healthy doses of life since 1949.
When you operate in an industry like pharmaceuticals, your work goes way beyond creating ‘products for customers’. It is different from any other domain – there lies a higher sense of responsibiliti and a need for utmost integriti
in everything you do. As you serve millions of lives, high qualiti standards become a pre-requisite, and safeti of your people and consumers always comes first. All this, while ensuring that each life you touch is treated with respect and dignity.Apply Online Via LinkedInÂ
Possible Interview Questions & Answers for the above job role:Â
What is your experience with Quality Management Systems (QMS)?
Answer: I have a good knowledge of QMS activities, including developing and maintaining quality policies, procedures, and manuals, conducting audits, and identifying areas for improvement.
2. Can you explain your experience with Critical Control Points (CCP)?
Answer: Yes, I have a good knowledge of CCP, which involves identifying and monitoring critical points in the production process to ensure product safety and quality.
3. What is your experience with Validation activities?
Answer: I have a good knowledge of validation activities, including process validation, equipment qualification, and cleaning validation, to ensure the consistency and reliability of our processes and products.
4. Can you give an example of how you have performed a risk assessment in the past?
Answer: Sure, I have conducted risk assessments to identify potential risks and hazards associated with our products and processes, such as analyzing raw material suppliers, manufacturing processes, and product packaging.
5. How do you stay up-to-date with the latest industry standards and regulations?
Answer: I regularly attend industry conferences and seminars, read trade publications and regulatory updates, and participate in professional development programs to stay informed about the latest trends and regulations in the pharmaceutical industry.
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