Cipla QC Pharma Job Opening – Online Application Process
Cipla QC Pharma Job Opening – Online Application Process. M.Sc. / B. Pharma candidates can apply for a Quality Control Job at Cipla. Cipla QC Pharma Careers. Interested and eligible applicants can check out all of the details on the same below
Job role: Junior Team Member – QC (77156)
Job ID: 77156
Job Type: Full time
Location: Rangpo
About the company:
At Cipla, we constantly work towards ensuring access to high quality and affordable medicines to support patients in need. Which is why, we have been trusted by health care professionals and patients across geographies for the last 8 decades.
Job Description:
Job Purpose
Prepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP requirements
Accountabilities
- Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis
- Review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopeia through consent with regulatory body
- Review the assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements
- Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit
- Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed
Competencies/Skills:
- Communication Skills (clarity of thought, comprehension)
- Likely potential for growth
- Job / Product / Technical Knowledge / Pharma domain knowledge
- Presentation & Interpersonal skills (If applicable)
- Managerial or People Management skills
- Safety awareness (If applicable)
- Relevance of Previous Experience
- Comprehension, Analytical & Problem solving abilities
- Productivity & Result Orientation (If applicable)
- Attitude
- Qualification fitment
- Sales drive (If applicable)
- Personality traits (Individualistic / Team player, Outspoken, Maturity level etc.)
Division: Quality
Department: Quality Control
Experience: 2 years of experience in QC department of a pharmaceutical organization
Education Qualification: M.Sc. / B. Pharma
Hey there! Here are some interview questions for the role of Junior Team Member – QC (77156).
- Can you tell us about your experience in quality control within the pharmaceutical industry? Answer: I have been working in the quality control department of a pharmaceutical organization for the past two years. During this time, I have gained hands-on experience in performing various quality control tests, analyzing materials, and ensuring compliance with quality standards and regulatory requirements. I am familiar with operating sophisticated laboratory equipment, documenting results, and maintaining accurate records. My experience has provided me with a strong foundation in quality control principles and practices within the pharmaceutical industry.
- How do you ensure compliance with pharmacopeial updates and regulatory requirements in your work? Answer: I understand the importance of staying updated with the latest pharmacopeial updates, supplements, and amendments. To ensure compliance, I regularly review and evaluate these updates to identify any changes required in the existing documents, such as SOPs and specifications. I also maintain close communication with the regulatory body to seek their guidance and consent when necessary. By proactively monitoring and incorporating these updates into our quality procedures, I ensure that our work aligns with the current pharmacopeia and regulatory standards.
- Could you describe your approach to preparing and reviewing documents like SOPs and specifications? Answer: When preparing documents like SOPs and specifications, I follow a meticulous approach. I thoroughly research the relevant information and consult subject matter experts to gather comprehensive and accurate data. I then organize and structure the information in a clear and concise manner, ensuring that it aligns with predefined quality parameters and compliance requirements. During the review process, I refer to supporting documentation and quality procedures to ensure that the documents meet the necessary quality standards. Attention to detail and adherence to regulatory guidelines are key aspects of my document preparation and review process.
- How do you ensure the availability and accessibility of documents across the site? Answer: Ensuring the timely availability and accessibility of documents across the site is crucial for smooth operations. To achieve this, I maintain a well-organized document management system. I issue documents to the applicable units while keeping a record of the issuance in a bound book. This record helps track the current version of common documents available at each unit. Additionally, I actively collaborate with relevant teams to establish efficient communication channels and provide necessary support during the analysis. By implementing these practices, I contribute to the seamless availability and accessibility of documents throughout the site.
- How do you approach the harmonization and simplification of documents to ensure standardized procedures? Answer: Harmonization and simplification of documents play a vital role in reducing complexities and ensuring standardized procedures. To achieve this, I conduct thorough evaluations of existing documents and processes. I identify areas where standardization can be improved or redundancies can be eliminated. I then collaborate with cross-functional teams and subject matter experts to develop streamlined and simplified procedures that align with industry best practices and regulatory requirements. By actively promoting harmonization and simplification, I contribute to enhancing process efficiencies and maintaining consistent quality standards.
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