Johnson & Johnson was founded more than 120 years ago on a revolutionary idea: Doctors and nurses should use sterile sutures, dressings and bandages to treat peoples’ wounds. Johnson & Johnson is ranked by Fortune Magazine as the 3rd most Admired Pharmaceutical Company in the world with an outstanding product range as well as an extensive research base with a number of life saving original research molecules.
Janssen Cilag, the pharmaceutical business of Johnson & Johnson has a presence in high growth pharma markets like Oncology, Nephrology, CNS, Gastroentrology, Dermatology, Neurology, and Gynecology among others.
Post : Senior Officer- Supplier Quality
Job Description
• Global /Regional Quality Agreements: Requires connecting with senior executives of large global organizations and discussing /negotiating the agreement.
• Specification Review: Review of the Raw Material Specifications from compliance standpoint and ensuring accuracy before approvals.
• Independent Leadership on Select Global Suppliers and dealing with issues faced on Quality Assessments / COA/ Compliance documents directly (E.g. Dow and BASF)
• Managing Quality agreements (Local/Regional/Global). with Suppliers and Consultants as J & J Account Lead.
• Coordinate on the Supplier quality related activities with sites in the APAC Region.
• Support coordination of Supplier quality issues using software package Symphony for managing quality system compliance viz. Change Control, Non-Conformance & CAPA Management.
• Supplier Audit Planning /Coordination and conducting the cGMP audits.
• Preparation/compilation of monthly reports for management information. Coordinate with sites to collect the information for reporting purpose, in timely manner.
• Coordinate/ Provide support to new product development projects/ Sourcing Strategy related projects and other quality improvement projects.
• Managing the Quality Review of Raw Material Specifications.
• Handles Quality issues by personal intervention to drive to resolution.
• Support on deployment of global and regional guidelines/standards at Suppliers.
• Coordinate training programs for suppliers.
• Managing Open Escalations, Risk Assessment Actions, Status follow up and Monitoring Exit Strategy progress.
• Leading the Supplier Risk Assessments process.
• Managing CAI and EAI rated global supplier’s status.
• Leading the Supplier Risk Assessments for APAC region.
• Driving Quality Expectation through SUMMIT process.
• GMP/Quality Audits planning, coordination and remediation for API & Chemical Supplier.
Candidate Profile
Education: M. Pharm or M.Sc in Chemistry from a reputed college/university
Experience: Around 4-6 years in the Supplier Quality Management/Quality Assurance function of a Pharmaceutical/Healthcare Company.
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Skills Required
• In-depth knowledge of cGMP and other applicable regulations of the different regulatory authorities.
• Working knowledge of analytical chemistry, chemical processes. Able to apply this knowledge in combination with quality system requirements to evaluate and (if applicable) to support the development of quality systems at the different suppliers.
• Clear, specific and concise verbal and written communication skills.
• Ability to build up interdependent partnerships with excellent interpersonal interaction skills particularly the ability to interface with multiple non-J&J business partners and in some instances, influence without direct authority.
• Ability to balance multiple tasks, objectives and priorities.
• Ability to lead cGMP Audit of suppliers.
Additional Information:
Experience: 4-6 years
Location: Maharashtra-Greater Mumbai
Education: M. Pharm or M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Quality Assurance
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