Job summary
Job post source
This job is directly from SUN PHARMA
Job overview
The Manager, Quality Assurance at SUN PHARMA oversees quality assurance functions ensuring compliance with cGMP standards and regulatory requirements in pharmaceutical manufacturing.
Responsibilities and impact
The role involves managing QA staff, conducting training, preparing for FDA inspections, ensuring compliance in manufacturing and testing, managing budgets, leading investigations, supporting audits and certifications, and maintaining quality systems.
Experience and skills
Requires an advanced degree in Chemistry or related field, at least 5 years of QA/QC experience in a cGMP/API environment, prior management experience, and proficiency in Microsoft Office Suite.
Company overview
Sun Pharma is a global pharmaceutical company headquartered in Mumbai, India, specializing in the development, manufacturing, and marketing of a wide range of pharmaceutical formulations and active pharmaceutical ingredients (APIs). The company generates revenue through the sale of generic and branded medications across various therapeutic segments, including cardiology, psychiatry, neurology, gastroenterology, and diabetology. Founded in 1983 by Dilip Shanghvi, Sun Pharma has grown through strategic acquisitions, including the notable purchase of Ranbaxy Laboratories in 2014, making it one of the largest generic drug manufacturers in the world.
How to land this job
Position your resume to highlight your management experience overseeing Quality Assurance teams, emphasizing goal setting, performance reviews, and training initiatives specific to cGMP/API environments.
Focus on your expertise in regulatory compliance, especially your role in FDA inspection preparation, quality system monitoring, and handling quality investigations and audits.
Apply through multiple platforms including the SUN PHARMA corporate careers page and LinkedIn to maximize your application’s visibility.
Connect with current SUN PHARMA Quality Assurance or Compliance team members on LinkedIn; start conversations by referencing recent regulatory challenges the company faced or by asking about their experience with cGMP training programs.
Optimize your resume for ATS by incorporating keywords from the job description such as 'cGMP', 'FDA inspection', 'Quality Assurance management', 'validation program', and 'APQR program' to ensure it passes automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify the best portals for submission, and find relevant SUN PHARMA contacts to network with, allowing you to focus on interview preparation and skill enhancement.
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