Manager-MSTG

**Job Title:-**Manager-2

**Business Unit:-**MSTG

**Job Grade-**G11A

**Location:-**Paonta Sahib

At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

JOB RESPONSIBILITES

• To ensure co-ordination and timely execution of feasibility, process development, registration, exhibit, pilot bio-batches and PPQ batches.
• To ensure SOP and cGMP compliance in Master Documentation.
• To maintain review of master batch production records and SOPs.
• To ensure QMS activities including deviation, OOS, change controls and CAPA implementation.
• To ensure quality, purity, safety and identity of drug product in accordance with MI.
• To monitor manufacturing and cleaning activities in different process areas.
• To ensure planning and procurement of change parts and raw materials.
• To maintain and control RM warehouse inventory of PDL at Paonta Sahib location.
• To maintain FO/MI, protocols, reports and technology transfer documents.

Initiation of Documents

• Protocols and reports for feasibility, development, exhibit and PPQ batches
• FO/MI of exhibit, PPQ, registration and pilot bio batches
• Track-wise documents: PD, UPD, investigations, CAPA and change controls
• Creation/extension/deletion of RM, API and INTM codes
• Purchase requests and SAP related activities
• Analytical requests and additional test requests
• EDMS related document generation and revisions

Review and Approval Responsibilities

• Review and approval of protocols, reports, FO/MI documents, SOPs and other GMP related documents.

Accountability

• Execution of feasibility, development, registration, exhibit/PPQ and pilot bio-batches
• Timely procurement of materials and change parts
• Response to regulatory queries
• Completion of investigations, deviations, OOS, CAPA and change requests
• Support for internal and external audits
• Warehouse inventory management and transfers
• cGMP compliance in master documentation

Job Requirements

**Educational Qualification: -**M.Pharma

**Experience:-**Experience- Tenure -: 8-12 Years

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).