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Associate Regulatory Operations

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  • Posted 5 days ago
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Job Description

JOB DESCRIPTION:

Primary Job Function:

Supports EPD Regulatory Affairs (EPD-RA) by taking responsibility for the following activities:

  • Maintaining and managing documents in Document management system. Responsible for managing the workflow and version controlling of the documents in the system
  • Support document formatting using MS word functionalities, styles, recommended formats as needed
  • Support making PDF document submission ready by use of PDF feature and ISI Toolbox plug-ins
  • Performing quality checks of documents (format perspective)
  • Supports submission compilation of documents into submission binders
  • Fixes Best practices to make the documents submission ready
  • Interacts and coordinates with key stakeholders like Regional Product leads, affiliates, CMC and other Global Regulatory Strategic teams
  • Manages the country specific dossier structure across varied regions (especially non eCTD countries)
  • Maintains request level data through effective trackers which is used for Monthly reporting of the data
  • Exhibit team spirit and manage timely delivery of importing of documents into Document Management system or any other ad hoc requests in time
  • Training new DARIUS users and/or new team members as and when requested
  • Support any other operational activities based on business needs as and when requested

Specific actions and responsibilities of individual contributor includes but are not restricted to:

-Supports prioritised projects and activities across EPD RA

-Monitors and communicates actual versus planned activities and timelines

-Identifies and communicates risks and issues impacting day-to-day activities

-May represent Regulatory Operations at relevant project meetings and communicates agreed GRA position

-With manager agreement, provides submission compilation support for Regional and Affiliate colleagues

. Compliance across Life-Cycle

-Provides support for submission compilation and building of registered positions in DARIUS

-Takes steps to identify, communicate, and mitigate risks

-Identifies opportunities and suggests improvements

-Has extensive knowledge of processes and systems such as DARIUS used within EPD-RA

CORE COMPETENCIES

-Works with manager to define short-term (days) work tasks

-Works with manager to regularly review the status of work tasks

-Reacts quickly to solve problems and issues when they arise

-Attempts to anticipate, mitigate and avoid problems and issues

-Seeks feedback from manager and team members and adapts behaviour to improve performance

-Is aware of the need to develop an intrapreneurial mindset to identify new or unique ways to address work problems or opportunities

-Delivers high quality results.

-Meets agreed deadlines.

-Exhibits honesty and presents complete impartial information.

-Displays consistency between words and actions.

-Acknowledges and responds constructively to failures and mistakes.

-Expresses dissatisfaction constructively, without over-reacting.

-Interacts with colleagues to complete team and shared goals

LEADERSHIP COMPETENCIES

-Provides information to Document Operations colleagues and business partners to build strategies

-Shares knowledge and previous experience with peers

-Completes goals according to agreed deadlines

-Provides information to help with decision-making within scope of project/product responsibilities

-Provides honest, accurate feedback to colleagues, whether positive or negative

-Not afraid to challenge peers and be challenged

-Openly shares information with peers

Supervisory/Management Responsibilities:

Direct Reports None (individual contributor)

Indirect Reports: None (individual contributor)

Minimum Education:

Bachelor's Degree in pharmacy, biology, chemistry, pharmacology, or related subject

Minimum Experience/Training Required:

A minimum of 5 years of experience in Regulatory Affairs, R&D, Manufacturing or related areas

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Regulatory Operations

DIVISION:

EPD Established Pharma

LOCATION:

India Mumbai : Mumbai Development Center - EPD

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Not specified

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

More Info

About Company

Abbott Laboratories is an American multinational medical devices and health care company with headquarters in Abbott Park, Illinois, United States. The company was founded by Chicago physician Wallace Calvin Abbott in 1888 to formulate known drugs&#x3B; today, it sells medical devices, diagnostics, branded generic medicines and nutritional products. It split off its research-based pharmaceuticals business into AbbVie in 2013. The firm has also been present in India for over 100 years through its subsidiary Abbott India Limited, and it is currently India's largest healthcare products company

Job ID: 145789673

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