Senior Manager- Quality Assurance

Reposted 5 Days Ago
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Mumbai, Maharashtra
In-Office
Expert/Leader
Healthtech
The Role
Lead LLM Operations and ensure compliance with GMP and Abbott policies through team guidance, audits, and cross-functional stakeholder management, while managing quality processes at loan license manufacturing sites.
Summary Generated by Built In

     

JOB DESCRIPTION:

Primary Job Function:

  • Lead and guide the team for LLM Operations and functionality on GMP aspects and Abbott policies and procedures.
  • Monitor compliance of Loan license manufacturing sites and TPMs.
  • Perform LLM site visits on scheduled basis and ensure compliance of LLM sites to cGMP, Abbott policies and Procedures.
  • Ensure Pharmacopoeial compliance of Abbott products manufactured at LLMs.
  • Review ongoing stability data and control samples of Abbott products.
  • Ensure implementation of Abbott quality audit CAPA & closure at LLMs.
  • Ensure timely investigation of the Market complaints within SLA, root cause analysis, CAPA implementation and effectiveness check.
  • Coordinate with responsible CFT for NSQ’s, Govt Agency responses.
  • Review & assess change controls, deviations, OOS/Failures at LLM sites related to Abbott products.
  • Ensure QTA compliance at LLMs and ensure QTAs are in place for all LL/TPMs.
  • Monitor and support projects as assigned by the Manager.
  • Ensure review and approve documents for tech transfer projects @ TPMs and FLQR review and approval for all projects for existing products and changes.
  • Review of change controls and approval for products at TPMs in Abbott system.
  • Tech Transfer at TPMs including Analytical method transfer, FLQR (First Lot Quality Review )
  • Ensure and review GSR notifications and timely compliance at TPMs impacting Abbott products
  • Ensure an effective communication process within cross functional team for execution of Quality projects supporting India Business.
  • Ensure compliances related to regulatory changes impacting Abbott products and processes.
  • Recruit, mentor, train and develop TPM QA India team members.
  • Manage the CFT stakeholders including S& OP meetings, lead from the quality front.
  • Ensure Deloitte Compliance across all LL sites including implementation of Abbott’s processes and compliance across all LL sites in coordination with LL site management

Data Management           

  • Ensure all TPM and product related database is maintained and achieved for the TPM QA function.
  • Customize Quality related procedures and Work instructions for the region as required for local requirement and its periodic review/ updates/ additions of SOPs to continuously improve processes and ensure compliance

             

Stakeholder Management

  • Set and manage of expectations with stakeholders (Commercial, Planning,  TPMs, MS&T, Regulatory, Labelling w.r.t Quality and Regulatory compliance.
  • Support AVD projects for loan license sites and materials for requirement as per Abbott process and policies.

Expectations & Skills :

  • Leverage knowledge, people networks inside and outside the company, out of the box thinking to resolve problems impacting Quality and regulatory challenges etc. impacting Abbott business.
  • Flexible, proactive and motivated by the opportunity to optimize structures and processes
  • Works collaboratively with colleagues to achieve organizational goals
  • Ability to adapt in a high pressured an ever-changing business environment
  • Ability to constructively cope with conflicts
  • Strong and proven analytical, organizational and decision-making skills
  • Strategic thinking, result and compliance oriented
  • Good interpersonal and communication skills
  • Resolution driven with adequate technical expertise
  • Ability to work efficiently in complex and deadline-driven operations, not losing focus on accuracy and quality
  • Proven track record to set priorities and adapt them accordingly at short notice
  • Effectively work on multiple, unrelated projects simultaneously
  • Provide expert guidance to team and CFTs on quality aspects and requirements supporting business
  • GMP and Regulatory requirement, TPM Management, Due diligence.
  • Ability to influence others. Intercultural competence.
  • Ability to understand the impact of business development decisions and contractual language on the Operations organization.
  • Ability to handle large volumes of confidential information and data and be able to determine how and when to inform upper management on quality related matters. Have a good control on Product database related to Quality.

Team Management          

  • Develop a high-performance team by continuous monitoring and provision of guidance to develop the team
  • Identify improvement areas and conduct/drive initiatives for training sessions to upskill people to ensure functional knowledge of process.

Supervisory/Management Responsibilities:

Direct Reports:   - 02

Indirect Reports:  - Contingent Workers @ LLMs ( Around 50 for SAP users management)

Position Accountability/Scope:

  • Key contact for Quality aspects for Loan License products.
  • Support and navigate to CFTs for Quality related matters for impacted products
  • Quality Technical Agreements.
  • Compliance to Abbott procedures and policies.
  • Tech Transfer and FLQR
  • Metrics review and management.
  • Change Control Management
  • Understand the overall Quality policies and EQDs and its implementation in India as per Global procedures.
  • Ensure an efficient exchange of information and a close working relationship with the CFTs for regulatory and Pharmacopoeial changes impact ting Abbott products
  • Provides guidance to LLM/TPMs for the compliances and investigation support for quality failures like Market compliant investigations, OOS, OOT.
  • Establish and maintain an expanded network of contacts to share best practices, expertise related to Quality and Regulatory changes.
  • Promote quality and compliance, simplification and standardization in global TPM QA

Leadership / Team leading:

  • Lead cross-functional, key contact for Quality Aspects to support business.

Minimum Education:

  • B Pharm /M. Pharm / Master in Science
  • Any additional education is an added asset.

Minimum Experience/Training Required:

  • 12 to 15 years of experience in Quality Control / Quality Assurance,  QMS, R&D QA, TPM Management, Tech Transfer, Dossier review, Due Diligence of products and sites.
  • Required to have managed TPM’s in a significant

Languages:

  • Proficiency in English
  • Other languages are advantageous

     

The base pay for this position is

N/A

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

     

JOB FAMILY:Operations Quality

     

DIVISION:EPD Established Pharma

        

LOCATION:India > Mumbai : BKC Building

     

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)

     

     

     

Top Skills

Analytical Method Transfer
Gmp
Quality Management Systems (Qms)
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The Company
Abbot Park, IL
97,838 Employees

What We Do

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.

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