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Sterile Production Supervisor
2 months ago
Grand River Aseptic Manufacturing is seeking a highly skilled and experienced Manufacturing Supervisor to join our team. As a key member of our operations team, you will be responsible for overseeing the day-to-day activities of our manufacturing department, ensuring that all production processes are carried out in accordance with established procedures and regulatory requirements.
Key Responsibilities- Leadership and Oversight: Provide guidance and direction to production staff, ensuring that all tasks are completed efficiently and effectively.
- Quality Assurance: Conduct regular audits to ensure compliance with cGMP regulations and company quality standards.
- Process Improvement: Identify areas for improvement and implement changes to increase efficiency and productivity.
- Communication: Collaborate with cross-functional teams to ensure seamless communication and coordination of production activities.
- Training and Development: Provide training and support to production staff to ensure they have the necessary skills and knowledge to perform their duties effectively.
- Education: Bachelor's degree in a life science or equivalent training and/or experience.
- Experience: Minimum 3 to 5 years of relevant pharmaceutical experience, with a strong understanding of cGMP regulations and regulatory compliance standards.
- Skills: Proficient computer skills in Microsoft Word, Excel, and Outlook, with experience in aseptic manufacturing of regulated products.
- Competitive Salary: Depending on experience.
- Benefits: Medical, dental, vision, life insurance, and disability benefits, as well as 401(k) program with immediate vesting.
- Paid Time Off: 17 days of time off per calendar year, plus one paid day of Wellness Time Off per quarter.
- Paid Holidays: 10 paid holidays per calendar year.