Production Supervisor - Weekend aproximadamente Novo Ver

Apresentação da empresa

Novocol Pharma is a growing contract development and manufacturing organization (CDMO), specialized in sterile injectable cartridges and combination product manufacturing. We strive for excellence and customer-centricity to deliver value to global pharmaceutical clients through contract services for drug development and commercial manufacturing. With over 40 years in operation, our team of 600 employees and modern facilities, located in Cambridge, Ontario provide a personalized and responsive experience for our customers.

We are focused on serving our strategic partners and patients with quality, integrity, and value.

Our employees are our number one asset! We offer developmental opportunities, excellent compensation and benefit programs, discounted gym memberships, work/life balance programs, employee recognition, social events and spirit days.

We are a proud member of the Septodont group of companies. Septodont is a pharmaceutical and medical device company with a global leadership position in dental pain management. The group counts over 2000+ employees worldwide and has remained a 100% family owned company for over 90 years. Our Cambridge facility serves as a significant manufacturing site within the Septodont group with high volume dental anesthetic production for a global customer base.

We have an oportunidade para um Production Supervisor I.

Location:

Cambridge, ON, On-Site

Employment Type:

Full-time

Schedule:

Weekend Day Shift, Saturday Sunday, Monday Tuesday.

The Production Supervisor I is an entry level position where the successful candidate will be provided with on-the-job training and coaching to develop into the Production Supervisor II role. The Production Supervisor I is responsible for assisting the Production Supervisor II with the day-to-day operations including employee performance, machine efficiency, and improvement initiatives to facilitate enhanced productivity.

The successful candidate will follow a structured training program that is focused on Standard Operating Procedures, Good Manufacturing Practices, learning and understanding the pharmaceutical manufacturing environment, and developing into an effective leader who demonstrates key leadership competencies with a focus on Septodont’s vision, mission, and values.

PRIMARY DUTIES AND RESPONSIBILITIES:

• Supports coordinating shift changeover by ensuring:
  • Machinery and human resources are optimal and report any deficiencies in a timely fashion.
  • Availability of components and supplies.
  • The Production Areas are clean and organized.
• Maintains a visible presence on the production floor and assists in resolving issues related to production/output.
• Assists with Monitors job duties to ensure that all pertinent SOPs are followed and all activities are documented properly.
• Works with the Production Supervisor II to issue, investigate and rectify Quality Assurance deviations, including:
  • Revising departmental SOPs and other GMP documents.
  • Fixing documentation errors and coaching related operators on documentation practices.
• Maintains a high degree of co-operation with other departments and participates in cross-departmental activities.
• Acts as a resource to educate and train direct reports on the Safety Program. Holds employees accountable for following safety rules / regulations.
• In conjunction with Production Managers and the Human Resources Department, support Employee Relations activities such as: assisting in the completion of employee performance reviews, monitoring performance improvement initiatives and guiding employee improvement action plans, supporting the administration of disciplinary action, and guiding conflict resolution by assisting in the investigation of employee complaints and recommending suitable resolutions.
• Coordinates new employee training and other training requirements of production staff through reviewing identified training gaps and supporting cross training plans.
• Ensures GMP and regulatory requirements and confirms quality standards are met.
• Completes Batch Record Reviews and daily shift reports for output, efficiency, downtime and other required matrices.
• Models…