B.Pharma, M.Sc Vacancy at Cipla

Overview:

Cipla is hiring experienced candidates for the post of Junior Team Member at their Goa, location.The Junior Team Member are responsibilities for handling all tasks assigned by the team leader or manager, working synergistically with other team members.

If any candidates are interested in this post then you can apply. There is 01 vacancy for the above position, as per the official website notification. Candidates are advised to read the eligibility criteria before applying for this post. The selected Candidate works in the Finance Department. Eligible and desirous candidates apply through the official website of Cipla. There is no age limit to apply for this post. Interested candidates must first visit Cipla official website, click on the career option, and then complete and submit your application.

The complete details of this job are as follows

Roles and Responsibility:

Accountabilities:

• Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
• Review Master Validation protocol and report for timely execution of validation batches and
  timely submission of documents in order to response for deficiencies
• Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
• Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
• Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
• Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
• Prepare final draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements
• Collect, compile and review raw data and finalise the same for timely submission of MHRA, UK interim update document to corporate as per agency requirement by tracking interim updates at a site level, for risk based inspection planning
• Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP
• Execute on time and errorless submissions by reviewing product license, all certificates for product registration and tender , staff approvals and other applications to adhere to legal requirements
• Support in CDSCO and state FDA inspection to be GMP compliant and getting product licence, FDA stall approvals by ensuring cross functional interaction

Qualifications for this Job:

• Must have B. Pharma, M.Sc from a recognized University.

Experience:

• Must have 2 years of experience in quality assurance department

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.)

Disclaimer: The Recruitment Information provided above is for informational purposes only. The above Recruitment Information has been taken from the official site of the Organisation. We do not provide any Recruitment guarantee. Recruitment is to be done as per the official recruitment process of the company or organization posted the recruitment Vacancy. We don’t charge any fee for providing this Job Information. Neither the Author nor Studycafe and its Affiliates accepts any liabilities for any loss or damage of any kind arising out of any information in this article nor for any actions taken in reliance thereon.