Component Prep Operator - CONTRACT

Vacancy details

General information

Reference

2025-2038  

Position description

Category

Operations - Manufacturing

Job Title

Component Prep Operator - CONTRACT

Company Details

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 opportunity for Component Prep Operators ON A TEMPORARY CONTRACT BASIS.

DAY SHIFT / AFTERNOON SHIFT / NIGHT SHIFT AVAILABLE

Job Summary

The Component Preparation Operator is accountable to the Production Supervisor for all activities relating to inspection, labeling and packaging of filled products. As well, preparation of glass caps and stoppers to meet the company’s objectives. This will be performed in accordance with the requirements outlined in Standard Operating Procedures and Good Manufacturing Practices.

Responsibilities

 

  • Reports any equipment problems to Lead Hand and Supervisor.
  • Completes Batch Record and log books.
  • Follows inspection, labeling, packaging and component preparation SOPs for preparation of components.
  • Inspects, labels and packages filled cartridges according to the appropriate SOP.
  • Performs and records all line clearance and cleaning.
  • Performs fill volume and seal integrity testing
  • Maintains Inspection Certification
  • Respectful
  • Collaborates with other departments to improve efficiency and reduce waste 
  • Follows GMP and regulatory requirements, and ensures quality standards are met. Observes and supports all safety guidelines and regulations
  • Models the Company Mission, Vision and Values Statements, policies, and current standard    business practices.
  • Performs other related duties as required.

Qualifications

Education

  • High school diploma. A college certification/diploma or equivalent is an asset.

Experience

  •  A minimum of 1 year related work experience in a manufacturing environment.

Contract type

Contract

Position location

Job location

North America, Canada, Cambridge