Production Coordinator

2 weeks ago

Bowmanville East, Canada Thermo Fisher Scientific Inc. Full time
Work Schedule

Environmental Conditions

Job Description

Summary: Participates in departmental projects by drafting

GMP documents

;

assists

in continuous improvement (CI) initiatives in production by compiling data,

observing

operations

and

identifying

potential improvements and solutions

.

Assists Production Management with

maintaining

metrics and tracking key performance indicators (KPIs);

Standard Operating Procedures (

SOP

)

review and revision.

Essential Functions: Support

s

procedure changes stemming from continuous improvement initiatives.

Provide

s

support

of

critical deviation investigations and plans to minimize deviation impact.

Supports

small projects in the

department

Develop

s

project management plans and

schedules

Explore

s

production efficiency improvement

ideas

Maintains a safe working environment and reports potential hazards.

REQUIRED QUALIFICATIONS

Education: H

igh school diploma/

General Educational Development (GED) Certificate is

required Working towards College Diploma or University Degree in Science

Experience: Requires no

previous

experience

.

Equivalency

: Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge,

Skills

and Abilities: Strong written and verbal communication, interpersonal, teamwork, and organizational skills.

Detail oriented with a focus on accuracy

.

Works well with limited supervision and takes full ownership of assigned work.

.Excellent

time management skills

.

Project management skills preferred

.

Proficiency

in Microsoft Office products (including Word, Excel, and PowerPoint).

Proficiency

with the English language.

Standards and Expectations: Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members, modelling positive team principles and partnering to meet project and departmental

objectives

. Carry out all duties within strict compliance

to

Patheon quality systems S

tandard Operating Procedures (S

OP

s)

and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems to

maintain

a smooth and efficient workflow (visual management, scheduling systems, etc.).

Be client and patient conscious at all times

.

Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for system improvements and engage in problem solving.

Models positive thinking and is open to change, motivating the team to adapt to shifts in priorities and new ways of working. Proactively

identify

areas for improvement in the execution of procedures. Communicate risks to timelines in a proactive manner. Consistently strives to improve skills and knowledge in related

field

.

Physical Requirements: Light physical effort and fatigue. Walks,

sits

or stands for limited periods. May require occasional equipment operation including keyboard equipment. Lifts light items for limited duration. Typically

located

in a comfortable indoor area

.

There may be exposure to mild physical discomfort from factors such as dust, fumes or

odours

, temperature extremes, loud noise, strong drafts, or bright lights.

Use of Personal

Protective equipment may be

required

and may include any of the following: s

afety glasses, safety shoes, lab coat, gloves,

hair net, beard cover,

safety apron, respirator

on occasionally

.

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