Maintenance Specialist

Septodont Croissy Beaubourg; Cambridge; On-site; CAD 70,000 - 90,000; Full time

Job summary

A pharmaceutical manufacturing company is seeking a Maintenance Specialist to enhance production equipment reliability and efficiency. The ideal candidate will have a Bachelor's degree in Engineering and 3-5 years of experience in manufacturing environments. Responsibilities include leading improvement initiatives, providing technical support, and ensuring compliance with safety and quality standards.

Benefits

Developmental opportunities

Discounted gym memberships

Employee recognition programs

Qualifications

• Bachelor's degree in Chemical or Mechanical Engineering is required.
• Minimum 3-5 years of manufacturing experience, preferably in pharmaceutical or food industry.
• Familiarity with Lean Manufacturing principles is a plus.

Responsibilities

• Provide technical support in manufacturing processes.
• Identify and lead continuous improvement initiatives.
• Maintain compliance with GMP and regulatory standards.

Skills

Problem-solving

Teamwork

Communication

Education

Bachelor of Engineering/Engineering Science

Tools

AutoCAD

MS Project

Job description

Company detail

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 a Maintenance Specialist

Job Summary

The Maintenance Engineer/Specialist is accountable to the Maintenance Manager for all activities related to maintenance project work and supporting production process at Septodont. The objective is to improve production equipment, maintenance, performance and reliability, through appropriate measurements, assessments, utilizing effective problem solving and improvement tools and executing on improvement actions and initiatives.

If the incumbent does not have the Professional Engineering Designation (P. Eng.), incumbent will use the title Maintenance Specialist an asset.

Responsibilities

·Provides ongoing technical support in any manufacturing processes as required

·Identifies opportunities for continuous improvement of production equipment and process in order to minimize downtime, turnaround time and waste reduction while maintaining the highest standard of quality.

·Recommends and leads continuous improvement initiatives based on OEE data analysis, focusing on preventive and corrective maintenance of equipment and systems.

·Assumes the role of Maintenance SME on new production equipment and actively participates in FAT/SAT/Commissioning and Installation activities of new equipment.

·Acts as liaison between the Engineering specialists/engineers and Plant Operations to ensure knowledge transfer for new production equipment

·Provides technical guidance to the Production Maintenance Team and support during breakdown investigations, with root causes analysis and actions.

·Initiates independent studies analyses on breakdowns, interprets maintenance data and develop actions plans/ conclusions.

·Supervises contractors and technicians on site for maintenance/repairs, equipment installations, and construction projects as needed

·Conducts risk assessments, writes technical reports

·Participates and contributes to RC analysis and support linked action plans

·Support quality investigations such as DIR’s, MDI’s and CAPA generation and execution.

·Identify trends and provide actionable insights to improve maintenance processes and equipment reliability.

·Analyze corrective maintenance activities and propose improvements to the preventive and predictive maintenance plans.

·Contribute to the spare parts plan for industrial equipment based on consumption, risks, and delivery times.

·Responsible for maintaining and updating lock-out tag-out (LOTO) procedures for the installed base of process equipment. Supports Engineering specialists/engineers in the generation and review of LOTO procedures for new equipment/equipment upgrades.

·Lead CAPEX projects of low complexity with a focus on improvement or parts obsolescence in alignment with Engineering.

·Designs, reformats and amends any Standard Operating Procedures (SOPs) as required.

·Prepares, revises and interprets conceptual layouts, as-built AutoCAD drawings and schematics for process and plant equipment as well as for GMP facilities systems.

·Maintains a high level of pharmaceutical compliance and regulatory safety in all aspects of work.

·Follows GMP and regulatory requirements, and ensures quality standards are met.

Perform other related duties as required

Qualifications

Education:

·Bachelor of Engineering/Engineering Science degree is a requirement (Chemical or Mechanical preferred)

·Professional Engineering designation (P. Eng) or working towards or completion of P. Eng designation

Experience:

·Minimum 3-5 years of experience in manufacturing environment, preferably in pharmaceutical, food/beverage or consumer packaging. 5+ years of experience considered an asset.

·Experience in a Lean Manufacturing environment is an asset.

·Able to read and interpret architectural, mechanical, electrical and P&ID drawings/schematics.

·Understanding of PLC’s / control systems on process equipment.

·Proficient in AutoCAD, MS Project, Word, Excel, PowerPoint.

·Excellent communication, interpersonal and organizational skills

·Demonstrates initiative, problem solver, team player and self-motivated

·Has the ability to lead and take ownership on systems and projects