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Head TPM QA

ConfidentialMumbai

20 days ago

Job description

Responsible and Accountable for the oversight of Quality operations and GMP compliance across the West and South EPD TPM s for, LL Systems & Contract Operations in India.

Effectively monitoring the rating of TPM / LL sites

Lead the implementation of quality strategy and plan in the above-mentioned sites including EQD policies implementation.

Implement Quality Projects at identified TPM s from time to time.

Ensure quality compliance to regulatory w.r.t. labelling, stability studies and documentation across the 4 business divisions to deliver acceptable quality products coming from LL and TPM sites to consumers on sustainable basis.

Develop strategy on quality as per Abbott`s EPD requirements for the Supply Chain

Organization in third party and LL manufacturing sites in applicable region.

Promote Quality Management System as an important management tool with increased

visibility across the business and guide the team for effective implementation at 3rd party

contractors.

Establish robust quality management systems through the supply network and ensure compliance.

Create culture which imbibes quality as a way of working through identified trainings and

awareness programs for critical LL and TPM sites.

Establish and implement a process to ensure all consumer complaints / queries are

addressed as per Abbott policy in stipulated time at applicable TPM sites.

Establish KPI s and analyse the same periodically to improve the compliance

metrics through departmental reviews.

Periodic quality reviews with COQA team.

Monitoring of LL & TPM tech transfers, SAP related matters and KPMG audit compliance.

Deputise for Director TPM QA as per needed

Ensure development needs are identified for direct reports

Ensure Quality budgets are maintained and managed for TPM QA organization

Ensure the COMPETE project runs as expected, efficiency and cost saving ideas are identified,

managed and implemented

Participate in 'Management Quality Reviews' and 'Functional interface meetings'.

Ensure that the associated TPM s are maintained in a state of Quality and compliance and the

CAPA;s arising out of the audits are closed on time.

Role : Quality Manager / Supervisor

Industry Type : Medical Devices & Equipment

Department : Quality Assurance

Employment Type : Full Time, Permanent

Role Category : Business Process Quality

Education

UG : Any Graduate

PG : MS / M.Sc(Science) in Any Specialization, M.Pharma in Pharmacy

Skills Required

Supply Chain, Sap, Tpm, Compliance, Pharma, stability studies , Contract Manufacturing, Gmp

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