BSc Chemistry & B Pharmacy Job @ Genpact - Candidates Apply Online

BSc Chemistry & B Pharmacy Job @ Genpact – Apply Online

Genpact is hiring B Pharma and BSc Chemistry candidates. Pharma job opening 2022. Regulatory affairs job opening 2022. Regulatory job opening 2022, Candidates with master’s degree and bachelor’s degree in pharma may check out all the details on our website Rasayanika.com

Job Title: Associate – Regulatory Affairs-LIF006966

Primary Location India-Mumbai

Eligibility Criteria:

• Bachelor’s degree, preferably in Pharmacy, Chemistry, Nursing or related discipline, required with relevant experience in the pharmaceutical industry. Alternatively, a Master’s or other advanced degrees, preferably in Pharmacy, Biological Science, Chemistry, Nursing or related discipline, required relevant experience in the pharmaceutical industry.

• Project Management expertise

• Understanding of regulatory requirements

• Excellent organizational skills and a proven ability to multi-task

• Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills.

• Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance).

• Demonstrated proficiency in advanced document management systems.

• Superior attentiveness to detail.

• Ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders.

• Flexibility in responding to changing priorities or dealing

with unexpected events.

• Capability to handle multiple priorities and balance work to achieve business goals.

• Effective leadership, communication, and interpersonal skills.

• Ability to prioritize tasks to meet deadlines and collaborate with a team when help is needed.

• Ability to identify problems and work with team to formulate a potential course of action

Responsibilities:

• Responsible to provide regulatory filing support for assigned Submissions by:
o Handling required submission activities (planning, obtaining required data (CMC/ancillary documents), coordination, reviewing, and release) in accordance to regulatory requirements and project timelines

  • Responding to health authority questions or local subsidiary requests for additional information to support the Submission
  •  Responsible for providing support for tracking regulatory submission documents.
  •  Work closely with various stakeholders to ensure timely follow-ups and receipt of documents for compiling submission packages in electronic/hardcopy format.
  •  Collaborative interaction to ensure quality, right-first-time output and timeliness.
  •  Monitor document availability status and escalate delays to avoid risk(s).
  •  Setting-up and coordinating meetings and managing submission activities.

Apply Online

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