Process Specialist 2

Septodont; Cambridge; On-site; CAD 75,000 - 95,000; Full time

Job summary

A leading pharmaceutical company in Cambridge is seeking a Process Specialist (II) to manage engineering projects and support process systems. The ideal candidate will have at least 5 years of experience in a manufacturing environment, with a Bachelor of Engineering degree. Responsibilities include leading engineering assignments, identifying improvements, and supporting R&D initiatives. This role requires strong communication skills and proficiency in relevant software tools. A permanent position is offered.

Qualifications

• Minimum of 5 years’ experience in manufacturing environment, preferably in pharmaceutical.
• Able to read and interpret architectural, mechanical, electrical, and P&ID drawings.
• Experience in the use of PLC’s/control systems on process equipment.

Responsibilities

• Manage and lead engineering assignments and projects from specification to turnover.
• Identify opportunities for continuous improvement in equipment and processes.
• Support relevant R&D projects and new product launches.

Skills

Excellent communication skills

Problem-solving

Team player

Self-motivated

Education

Bachelor of Engineering / Engineering Science degree

Tools

AutoCAD

MS Project

Word

Excel

PowerPoint

Job description

Job Summary

The Process Specialist (II) is accountable to the Technical Services Manager for all activities related to project work and supporting process systems at Septodont – Novocol Pharmaceutical Division. This includes supporting the ongoing business, capital and regulatory items in any process related area of the company.

Upon receipt of the Professional Engineer Designation (P. Eng.), incumbent may use the title Process Engineer.

Responsibilities

• Manage and lead varied engineering assignments and projects from specification to turnover which may involve the interaction with multiple departments.
• Provide ongoing technical support in any process area as required.
• Liaises regularly with internal customers to understand their technical service needs.
• Identify opportunities for continuous improvement of equipment and process in order to minimize downtime, turnaround time and waste reduction while maintaining the highest standard of quality
• Leads continuous improvement initiatives.
• Analyzes and supports validation for both a qualification and requalification activities.
• Support relevant R&D projects, and new product launches.
• Audits and approves protocols, drafts and executed reports.
• Initiates independent studies analyses and interprets data, and makes conclusions.
• Provides technical guidance to less experienced engineers, and technicians working on common projects.
• Writes commissioning and startup documentation.
• Designs, reformats, and amends any Standard Operating Procedures (SOP’s) as required.
• Prepares, revises, and interprets conceptual layouts, as-built drawings and schematics for process and plant equipment.
• Maintains a high level of pharmaceutical compliance and regulatory safety in all aspects of work.
• Works harmoniously with all fellow employees.
• Performs other duties as required.
• Supports the validation department in validation projects.
• 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 : Bachelor of Engineering / Engineering Science degree is a requirement (Chemical or Mechanical preferred).
• Experience : Minimum of 5 years’ experience in manufacturing environment, preferably in pharmaceutical, food / beverage or consumer packaging.
• Able to read and interpret architectural, mechanical, electrical, and P&ID drawings / schematics.
• 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.
• Experience in the use of PLC’s / control systems on process equipment.
• Experience in AutoCAD, MS Project, Word, Excel, PowerPoint.
• Experience in a Lean Manufacturing environment is an asset.
• Professional Engineer designation preferred.
• Able to travel internationally in support of projects (up to 20%)
• Contract type: Permanent
• Candidate criteria: Minimum level of experience required 6-10 years
• Position location