Cipla Job Opening BSc
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Cipla Job Opening BSc, MSc Life Sciences – Apply Online

Cipla Job Opening BSc, MSc Life Sciences – Apply Online. Graduate/Post Graduate in Life Sciences Jobs. Interested and eligible applicants can check out all of the details on the same below

Hey job seeker, if you are wondering what kind of interview questions you may have to answer for the role of Team Member – LCM at Cipla then make sure you reach the end of the page for those tidbits!

Name of the Post – Team Member – LCM

Requisition ID – 76888

Location – Vikhroli

Division – IPD

Department – IPD

Employment Type – Permanent

Job Purpose

Implement Life cycle management activities for Non-respi products (for US, EU, South Africa, ANZ, WHO, PEPFAR & 150+ countries ) to have Business continuity

Accountabilities

  1. Assess change request across the globe allocated by GL to review, evaluate and categorize the change as per regulatory guidelines to meet launches, commercial needs and compliance
  2. Prepare variation packages for modules 2 to 5 and deficiency response across the globe to support commercial launches, on-going commercial and regulatory compliance.
  3. Prepare annual report (US) as per schedule to meet regulatory compliance for business continuity.
    Prepare WHO requalification dossier to maintain product licence for business continuity.
  4. Compile re-registration dossier to maintain product licence for business continuity.
  5. Maintain and update product database for easy retrieval and status tracking

Education Qualification

Graduate/Post Graduate in Pharmacy or Life Sciences

Relevant Work Experience

5 years in the field of Regulatory Affairs/ Quality Assurance/ Quality control/ Manufacturing/ Analytical Development/ R&D

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, Out spoken, Maturity level etc.)

APPLY ONLINE

Hey you, before you run off to apply for this role, do check out the possible interview questions and their answers for the Team Member – LCM role at Cipla.

  1. Question: Can you explain the role of Life Cycle Management (LCM) in ensuring business continuity for non-respi products across different countries? Answer: Life Cycle Management involves assessing change requests, preparing variation packages, maintaining regulatory compliance, and updating product databases to ensure business continuity across global markets.
  2. Question: How would you categorize and evaluate change requests according to regulatory guidelines for commercial launches and ongoing compliance? Answer: I would carefully review each change request, assess its impact on regulatory compliance, and categorize it based on the specific guidelines provided. This evaluation process would consider factors such as safety, efficacy, quality, and documentation requirements.
  3. Question: Can you explain the importance of preparing annual reports and requalification dossiers for maintaining product licenses? How would you approach this task? Answer: Annual reports and requalification dossiers are essential for regulatory compliance and the continuous availability of product licenses. I would meticulously gather and compile the necessary information, ensuring adherence to specific regulatory requirements and timelines. This would involve thorough documentation, data analysis, and coordination with relevant stakeholders.
  4. Question: How would you maintain and update the product database for easy retrieval and status tracking? Can you provide examples of tools or systems you have used? Answer: I would employ robust database management systems and tools to maintain an organized and easily accessible product database. Examples of such systems include electronic document management systems (EDMS) or regulatory information management systems (RIMS). These tools facilitate efficient document storage, retrieval, version control, and tracking of the product’s status throughout its life cycle.
  5. Question: In your previous experience, how have you demonstrated your comprehension, analytical, and problem-solving abilities in the field of Regulatory Affairs/Quality Assurance? Answer: In my previous roles, I have actively participated in regulatory assessments, conducted comprehensive reviews of regulatory guidelines, and applied analytical thinking to evaluate and address complex regulatory challenges. I have successfully resolved issues related to compliance, quality assurance, and regulatory submissions by proposing effective solutions and implementing them with attention to detail.

Remember to tailor your answers to your specific experiences and highlight relevant skills and accomplishments. Good luck with your interview!

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