Manager -2

Sun Pharmaceutical Industries Ltd; Panchmahal District; On-site; INR 1,800,000 - 2,400,000; Full time

Job summary

Sun Pharmaceutical Industries Ltd in Halol is seeking a senior professional for the Manager - 2 position in Sun Global Operations. The role requires leading batch manufacturing activities, regulatory quality alignment, and cross-functional coordination to ensure CGMP-compliant production targets.

The candidate should have 15+ years of experience and hold M.Pharm or B.Pharma. Education details and experience play a crucial role in meeting customer and regulatory expectations at Sun Pharma.

Qualifications

• Educational qualifications required: M.Pharm or B.Pharma.

Responsibilities

• Prepare / initiate sign authority for batches and master batch manufacturing records.
• Coordinate risk assessment, process validation protocols, investigations, CAPA planning and closure.
• Support batch manufacturing and coordination of Aerosol department activities (MDI, DPI, Nasal Spray).
• Plan day-to-day production activities and allocate work to operators.
• Generate material work orders and coordinate with warehouse for timely material issuance.
• Coordinate with QC for in-process samples and COA releases.
• Coordinate with QA for line clearance, batch release, cleaning and process validation.
• Coordinate with Engineering for machine maintenance and preventive maintenance scheduling.
• Ensure CGMP compliance and overall production targets are met.
• Implement MBMR/MBPR/SOP/QP updates and qualification activities.
• Adhere to EHS requirements and CEP activities.

Education

M.Pharm /B.Pharma

Job description

Job Description:

Job Title: Manager - 2

Business Unit: Sun Global Operations

Job Grade: G11A

Location: Halol

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, you’ll 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.

Key responsibilities:

1. Preparation / Initiator sign authority for :
   • Commercial product / stability batches / exhibit batches / characterization batches– Master Batch Manufacturing Record.
   • Risk Assessment, process Validation protocol, incident and investigation report, action, compliance, and closure.
   • CAPA plans and closure.
   • Protocols & reports.
   • Internal Quality Audit/ Regulatory Quality Audit Compliance and closure.
   • Change control, Standard Operating Procedure, Planned Modification.
2. To assist the manager, DGM in batch manufacturingand controlling the functions related of Aerosol department - Manufacturing (MDI, DPI and Nasal Spray).
3. Responsible for the day to day production planning of department.
4. Work allocation to the operators as per production planning.
5. To generate the work order of raw material and packing material as per production planning and to co-ordinate with warehouse department for issuance of materials to achieve schedule plan.
6. To informed to quality control department for analysis planning of in process sample as per production schedule and co-ordinate with quality control (QC) department for release of in process and finished product COA.
7. To co-ordinate with quality assurance (QA) department for provide the line clearance on time, release of batch, cleaning & process validation.
8. To co-ordinate with engineering department for machine maintenance and preventive maintenance schedule.
9. Responsible for overall production activities, of the manufacturing area on daily basis in achieving total production requirements in quantity, quality with cGMP requirement.
10. Online filling of BMR, BPR of the batches and review of the same.
11. Monitor and control the operator for standardize production activity to achieve better productivity and quality.
12. Training the men-power to meet the organizational goals and achieve GMP compliance.
13. Review, updation & execution of MBMR / MBPR/ SOP /Qualification Protocol whenever is required.
14. Responsible for activity related to compliance enhancement programme (CEP) activity as when required.
15. Responsible for perform the qualification of new equipment and schedule qualification along with quality engineering (QE) department as when required.
16. To adhere with EHS requirement.

Job Requirements

Educational Qualification

M.Pharm /B.Pharma

Experience

15 +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).