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Teva Pharmaceuticals
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Senior Director, Site Quality Head, Goa

Senior Director, Site Quality Head, Goa

Teva Pharmaceuticals

10 - 14 years

0 Lacs

goa

Posted:6 days ago| Platform: Shine logo

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Skills Required

quality management quality assurance quality control compliance regulatory requirements gmp data integrity quality systems manufacturing operations pharmaceuticals manufacturing

Work Mode

On-site

Job Type

Full Time

Job Description

As the Senior Director, Site Quality Head at Teva Pharmaceuticals in Goa, India, your primary responsibility will be to provide Quality oversight for Manufacturing, Packaging, and Laboratory Operations. Your key responsibilities will include: - Leading the Quality organization on site, encompassing Quality Control, Microbiology, Quality Compliance, Quality Systems, and Quality Assurance Operations. - Ensuring the implementation and continuous improvement of a current Quality Management System. - Ensuring products are manufactured, released, and distributed in accordance with cGMP requirements and registered specifications. - Assessing and mitigating risks by identifying quality risks, defining proactive mitigations, and ensuring products are safe and effective before reaching the market. - Designing and implementing the Site Quality Program in collaboration with the Site GM and Corporate Quality. - Overseeing the delivery of necessary data to support Quality objectives and compliance. - Directing Quality Control activities, including laboratory operations and approval/rejection of materials. - Promoting a sustainable culture of quality throughout the site operation. Your qualifications for this role include: - Required: Bachelor's degree in Chemistry, Biology, or Pharmacy - Preferred: Master's or equivalent degree in Chemistry, Biology, or Pharmacy Key Requirements: - Minimum of 10 years of pharmaceutical manufacturing site quality operations and leadership experience. - Deep knowledge of cGMP requirements of local and major international authorities like EMA and US FDA. - Strong understanding of manufacturing, packaging, technology transfer, cGMPs, EU, ICH guidelines, and regulatory submissions. - Experience in Data Integrity and Compliance, Quality Systems, and leading organizational change. - Experience in developing and implementing efficient business processes and practical knowledge of pharmaceutical manufacturing and control. You will be a strategic partner in the site leadership team, ensuring project timelines are met and providing effective Quality leadership during inspections. Your role will also involve managing the Quality Operations budget and resources to maximize efficiency for the organization. If you are passionate about driving quality initiatives and have a proven track record of leading organizational change to improve efficiency, we encourage you to apply for this role at Teva Pharmaceuticals in Goa, India.,

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Teva Pharmaceuticals

Pharmaceutical Manufacturing

Tel-Aviv Petach Tikva

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Senior Director, Site Quality Head, Goa

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Senior Director, Site Quality Head, Goa