Title:  QC Section Head

Title:

QC Section Head

Business Unit:

Quality Control

Job Grade

Senior Manager

Location:

Paonta Sahib, H.P.

Key Responsibilities

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.”

JOB DESCRIPTION

Position Summary:

• Plan and monitor analysis of sample, lead laboratory investigation, conduct effective review of team and portfolio, provide direction and guidance to the team and develop team competence with the objective of ensuring release of batches with adherence to GMP compliance and quality matrix and timelines
• The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures.

Key responsibilities:

• Planning and managing analysis in different sections as assigned. (By techniques or material)
• Ensure completion of testing as per release schedule for materials and products.
• Oversee the activities in respective section such as analysis, review of analytical data, calibration, preventive maintenance and general trouble shooting.
• Participate in internal and external inspections at site as appropriate
• Facilitate method transfer to other sites.
• Ensure training is imparted to analysts as per assessed training need.
• To ensure optimum utilization of instruments and consumables.
• To prepare and publish monthly QC performance reports such as testing SLA, instrument utilization, OTIF, analyst and reviewer productivity
• To review and approve laboratory investigation such as OOS, OOT and lab events
• To ensure safety and cGLP practices are followed in QC lab
• To coordinate with cross functions at site such as Operation, QA and Warehouse for scheduling raw material and finished product analysis
• To coordinate with cross functions outside site such as third party testing lab, corporate functions and Analytical Development for testing, method transfers and troubleshooting,
• To ensure timely closure of QMS originated from QC lab.
• To perform trending of QMS generated from respective section and perform CAPA effectiveness review.

Required Success Attributes:

• Knowledge of GxP’s, cGMP and other regulatory requirements.
• Attention to detail
• Initiative
• Learning Agility
• Compliance

Secondary Success Attributes

• Collaboration
• Effective Communication
• Passion

Additional responsibilities can be assigned as required. 

Travel Estimate

Job Requirements

Educational Qualification

Science and Pharmacy Graduates or Equivalent

Experience

13+ years with QC work experience

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).