GSK is hiring B. Pharma/ B. Sc as a Quality Assurance Executive – Apply Now

[the_ad id=”9653″]

GSK Pharma is hiring motivated B. Pharm and B. Sc graduates for the position of Quality Assurance Executive in the Nashik region. This is a fantastic opportunity to join a leading pharmaceutical company and contribute to maintaining high-quality standards in healthcare products. If you have a keen eye for detail and a passion for quality assurance, apply now to advance your career with GSK Pharma.

Position: Quality Assurance Executive

Qualifications & Experience for QA Executive at GSK

• B. Pharma/ B. Sc
• Minimum of 3 years of experience in Good Manufacturing Practices (GMP) operations

Key Skills for QA Executive at GSK

• Previous leadership experience
• Experience addressing technical business solutions
• Strong verbal and written communication skills
• Proven experience assuring compliance with regulations

Job Description for QA Executive at GSK

• Are you energized by a Quality Assurance role that allows you to accelerate compliance in a highly technical and regulated environment? If so, this Operational QA Staff role could be an exciting opportunity to explore.
• As an Operational QA Staff, you will manage/lead/be responsible for working on the shop floor addressing quality issues during production shift operating hours. Additional responsibilities include supporting incident and deviation investigations, participation in internal auditing activities and batch record review.

Responsibilities for QA Executive at GSK

• Ensure products are produced to the correct specification and per the operating instructions for all markets.
• Participate in gathering data and providing quality insights for deviation and consumer complaint investigations.
• Assist in review and approval of finished goods batch documentation.
• Assist in level 1 and level 2 internal auditing programs.
• To ensure that all batch implicating issues are highlighted and resolved without delay to batch release and/or impact to compliance/regulatory requirements.
• Comply with all operational safety, process safety, environmental permits, Quality policies, procedures and training requirements.
• Ensure quality is managed on the operational floor, however unlike Quality Operations
• Technician role, this role will not be allowed to approve any master quality documentation, deviation investigations, validations, or any other quality documentation that requires the approval of the Quality Department.

MORE JOBS:  Research Opportunity for M. Pharma/ MS Pharma/ M. Sc as a Junior Research Fellow at NIPER – Apply Now

<<<<<<<<<<<<JOIN US>>>>>>>>>>>>>>>>

[the_ad id=”9395″]