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5 ProductLife Group Jobs
VAF 153 Consultant (RQC)
5-7 years
Kolkata, Mumbai, New Delhi + 4 more
1 vacancy
VAF 153 Consultant (RQC)
ProductLife Group
posted 8hr ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
Role Description:
The Associate Consultant works within the Regulatory, Quality & Compliance team to contribute to the regulatory, quality, and compliance consulting practice. The Associate Consultant is responsible for the preparation and submission of GMP Clearance applications as well as a range of compliance documents or related quality activities. The Associate Consultant also supports the delivery of a variety of projects, working closely with the Regulatory, Quality & Compliance Administrators, Associates, Associate Consultants, Consultants, Senior Consultants, Manager, Senior Manager, and/or Head of Business Unit to deliver a superior client experience and optimize project outcomes.
- Adherence to ProductLife Group s values, policies, and quality management systems.
- Perform compliance activities to meet ProductLife Group and client Quality objectives.
- Support audit requests as required.
- Manage and prepare GMP clearance applications for submission to the TGA and/or other regulatory agencies, as required.
- Provide regulatory, quality, and compliance support to clients relating to the registration/listing of pharmaceuticals, biologicals, and medical devices and the ongoing maintenance of these.
- Assist clients in responding to agency questions.
- Provide support to clients by assisting more senior members of the team with regulatory, quality, and compliance activities.
- Prepare, review, and update quality documentation.
- Provide high-quality work that contributes to client satisfaction and loyalty, leading to the optimization of repeat business and expansion of service provision across the Regulatory, Quality & Compliance service offering.
- Undergraduate qualifications in the pharmaceutical sciences or other scientific discipline.
- A minimum of 3 years of experience in Australian and New Zealand Quality or Regulatory Affairs, preferably in a commercial environment.
- Good knowledge of TGA and Medsafe legislation, regulations, guidelines, and working procedures is preferable.
- Reasonable computer literacy.
- Proven experience dealing with a high level of confidentiality.
- Good problem-solving and project management skills.
- Ability to work to deadlines.
- Attention to detail.
- Excellent written and spoken communication and interpersonal skills.
- Interest in the practice of consulting.
- An appetite for learning and development.
Employment Type: Full Time, Permanent
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What people at ProductLife Group are saying
What ProductLife Group employees are saying about work life
based on 9 employees
Flexible timing
Monday to Friday
No travel
Day Shift
ProductLife Group Benefits
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