Component Prep Operator - CONTRACT
Component Prep Operator - CONTRACT
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
General information
Reference
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 customercentricity 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 companys 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
Job location
North America Canada Cambridge
Employment Type
Contract
