Quality Manager(GMP)

• Perform and/or arrange QA/QC audits of the facility.
• Minimum of 10 years’ experience in Quality Control and Assurance in the nutritional supplement and/or pharmaceutical products manufacturing industry.
• Laboratory management experience is required.
• Knowledge of industry regulations, FDA, USP, AOAC and ICH guidelines to ensure compliance and maintain accreditations.

Are you looking to make a career change to a rapidly growing company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance and paid PTO. Does this position match your future career goals? Then this opportunity could be the right fit for you

• A positive workplace culture
• Competitive Salary
• Career Advancement opportunities
• Financial Growth

EDUCATION AND EXPERIENCE REQUIREMENTS:

• Bachelor’s degree in Science
• Minimum of 10 years’ experience in Quality Control and Assurance in the nutritional supplement and/or pharmaceutical products manufacturing industry.
• Laboratory management experience is required.
• Maintain a thorough understanding of GMP regulations.
• Oversee quality processes in manufacturing and packaging, including cleaning procedures across all facilities.
• Perform batch record reviews and manage product disposition tasks as needed.
• Analyze and review deviations, complaint investigations, and change controls.
• Lead internal and external audits related to the Microbiology Laboratory, developing strategies to address audit findings.
• Oversee product investigations and resolve quality-related concerns in manufacturing operations.
• Serve as the Management Representative for Quality when required.
• Develop and implement quality systems, including CAPA, design control, and process control, to ensure product compliance.
• Manage regulatory inspections and compliance efforts for contract manufacturers.
• Oversee preparation of and approval for all company SOP’s.
• Update, draft, or review Standard Operating Procedures (SOPs).
• Assist with reviewing supporting documentation to ensure accuracy.
• Oversee the entire vendor management process to ensure efficiency and compliance.
• Maintain and update the Vendor List and Approved Vendor List regularly.
• Review and approve audit reports submitted by third-party auditors.
• Strong computer skills, including MS Office (Word, Excel, PowerPoint.
• Strong knowledge of global regulations for commercial & clinical operations.
  Job Type: Full-time
  Pay: $110,000.00 - $120,000.00 per year

Benefits:

• Dental insurance
• Health insurance
• Vision insurance

Schedule:

• 8 hour shift

Work Location: In perso

Please refer the Job description for details