Clinchoice is hiring B. Pharma/ M. Pharma as a Regulatory Affairs Executive – Apply Now

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Are you a B. Pharma, M. Pharma, B. Sc, or M. Sc graduate looking to advance your career in regulatory affairs? ClinChoice is excited to announce openings for the position of Regulatory Affairs Executive in the Chennai region. This role offers a unique opportunity to work with a leading company in the pharmaceutical industry, ensuring compliance with regulations and contributing to the successful launch of medical products. Join ClinChoice to take your career to new heights and make a significant impact in the field of regulatory affairs. Apply now to become a key player in our esteemed team in Chennai.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts.

Job Title: Regulatory Affairs Executive

Education, Experience and Skills for Regulatory Affairs Executive at Clinichoice

• Bachelor’s / Master’s Degree in Pharmacy / Science or other relevant domains.
• Fundamental working experience of 2-4 years in RA/QA/AR&D/R&D/QC requirements.
• Awareness on the tools used in regulatory activities like publishing, artwork, change control management.
• Experience in managing a matrix environment.
• Proven experience in decision making and tight deadlines.
• Technically adept at using IT systems and software.
• Fast learner with proven ability to adapt to changing demands.
• Good knowledge of English, spoken and written.

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Main Job Tasks and Responsibilities for Regulatory Affairs Executive at Clinichoice

• Complete the assigned activities diligently, by using appropriate client specific standards and tools, confirming to regulatory submission milestones and applicable regulatory obligations.
• Provide operational support within the team to execute designated tasks associated with submission.
• Accountable for delivering designated submissions with quality and timely as per applicable policy, SOP/Work, instructions, guidelines, or service level agreement.
  Commit to completing required on-the-job training courses to ensure training compliance is preserved.
• Continuous improvement of selected processes relating to human health submissions and selected drug and non-drug specific projects and related activities.

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• Support activities related to Product License Portfolio in a timely and quality manner.
• Execute the assigned activities to ensure completion of project tasks and/or milestones.
• Capable of understanding and implementing the basic team effectiveness skills like commitment, feedback, trust, and teamwork.
• Apply necessary technical skills to complete the assigned regulatory operational activities to support submissions to global health authorities.
• Performs work in a structured environment under direction from supervisor.
• Exercises judgment to complete assigned tasks and has significant reliance on supervisor.
• Uses established procedures to perform assigned tasks.
• Participates and contributes as a team member and is responsible for certain team deliverables.

The Application Process for Regulatory Affairs Executive at Clinichoice

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

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