Johnson & Johnson Hiring Executive Regulatory Affairs & Packaging in Mumbai About Johnson & Johnson Johnson & Johnson is a global healthcare company committed to improving health and well-being through innovative products and solutions.
DESCRIPTION
Executive Packaging & Regulatory Affairs Designation of Employee: Sr. Executive Functional Department: Regulatory Affairs Reporting to: Associate Director /Sr. Manager – Regulatory Affairs Job Responsibilities: Packaging Technology Transfer- lead the activities involved in the technology transfer from packaging perspective:
- To support packaging material characterisation (Engineering Study), Shipping Qualification (Physical), Oversee Packaging validation.
- Prepare and review Protocols & reports, Development of Artworks, Master Packing Records
- Prepare specifications for primary, secondary, tertiary & ancillary packaging materials.
- Manage Master Packaging Record review.
- Issue the certified copies of MPR to relevant stake holders as well as manufacturing site.
- Documentation like Master copy, Certified copy and Obsolete copies.
- Checking proofs/shade cards of packaging materials against approved artworks.
- Management of documentation and distribution of approved proofs/shade cards.
- Keep the record of Approved Artworks & Proofs, Certified MPR in individual product files.
- Keep the records of imported product artworks in individual product files.
- Keep the records of packaging material codes for all printed packaging materials.
- Preparation, review and collation of documents of application for Import of New Drugs and Established Products
- Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents.
- Applicable knowledge of D&C Act, NDPS Act, Legal Metrology Rules etc.
- Preparation of additional information or responses as requested by regulatory agencies
- Prepare or maintain technical files as necessary to obtain and sustain product approval.
- Direct the collection and preparation of laboratory samples as requested by regulatory agencies.
- Preparation, review and collation of documents pertaining to application for following certifications: WHO-COPP, GMP, GLP, No Conviction Certificate, Manufacturing & Marketing Certificate, Performance Certificate, Import and Marketing Certificate, Market Standing Certificate.
- Management of Testing of Samples at private and government laboratories such as CDTL, NIB, IPC.
- Co-ordination with EM sites for P2P and Loan License products with respect to grant of fresh and renewal of licenses.
- Supporting RA activities for management of product lifecycle management and NPI for cluster countries
- Conversant with eSugam portal of CDSCO/DCGI and XLN portal of various state FDA.
- Other responsibilities as assigned which covers to review and retrieve data from Public Domain.
- Maintenance of Tracker of all various activities, status of submissions and approvals.
- Responsible for effective interaction with team members and support functions at various levels in the organization.
- Ability to grasp new concepts quickly and to assimilate and evaluate scientific data.
- Responsible for interaction & collaboration for effective implementation of responsibilities.
- Efficient in Computer skills, Management Reporting and Administrative skills, Communication skills.