Only 24h Left Set-up Operator I

2 weeks ago


Cambridge, Ontario, Canada Septodont Full time
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.

The company has an opening at its sterile injectable manufacturing facility in Cambridge, Ontario for a Set-Up Operator.

Job Summary

SHIFT: Afternoons
NUMBER REQUIRED: 1
JOB LEVEL: 6

If interested in this posting, please upload your resume to the Internal Job Application Site no later than: March 2, 2025.

The Set-up Operator I is accountable to the Production Supervisor for all activities relating to the set-up of all inspection, labeling and packaging (ILP) equipment, trouble-shooting, mechanical adjustments, and preventative maintenance, in order to meet the company's objectives. These activities will be performed in accordance with the requirements outlined in Company Policies, Standard Operating Procedures and Good Manufacturing Practices.

Responsibilities

1. Sets up and disassembles all inspection, labeling and packaging machines.
2. Trains new ILP operators on inspection machine, labeling machine and packaging line operation.
3. Performs basic trouble shooting, mechanical adjustments, interventions and preventative maintenance on the ILP machines.
4. Reports any equipment problems and process related downtime to the area Lead Hand, Maintenance Technician, and Supervisor and work together to solve them.
5. Ensures that the ILP areas run smoothly by informing the area Lead Hand and/or Supervisor when supplies are needed.
6. Makes suggestions for improving training programs and ILP area processes and participate in continuous improvement initiatives.
7. In the absence of the Lead Hand, performs back-up duties and responsibilities as assigned.
8. Monitors and reviews system entries, ensure that scanned data is accurate.
9. Creates maintenance work orders and requests using the CARL system.
10. Reviews batch record entries and assist with audit corrections.
11. Ensures all GMPs, SOPs, and company policies are followed.
12. Assists with Q-Note and DIR Investigations as required.
13. Takes on the role of the Operator as needed.
14. Follows GMP and regulatory requirements, and ensures quality standards are met.
15. Observes and supports all safety guidelines and regulations.
16. Demonstrates the Company Mission, Vision and Values Statements, policies, and current standard business practices.
17. Performs other related duties as required.

Qualifications

Education: High school diploma
Experience: A minimum of one year of related work experience in a manufacturing environment, however 2 years or more of work experience is considered an asset. Pharmaceutical, food, or cosmetic industry experience is considered an asset. Demonstrated mechanical experience or mechanical aptitude. The ability to work any shift in a 24/7 environment.

What we offer

Excellent compensation/benefits package.

- Bonus and reward programs
- Discounted gym memberships
- Programs supporting work life balance
- Employee recognition program
- Professional and personal development programs
- Social events and spirit days

We are committed to diversity and inclusion, and thank all applicants in advance; however, we will be corresponding only with those selected for an interview.

Internal Job Posting Grade 6. The due date for internal applicants to apply for this role is March 2, 2025.

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