Technical Writer II

Mississauga - Canada

Monthly Salary: $ 50800 - 76150

Posted on: 22 hours ago

Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard Office Hours (40/wk)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

Summary:

Prepare and revise master batch records (MBRs) for manufacturing and packaging and provides input supportsand assistancesthe Technical Operations Pharmaceutics & Process Technology (PPT) and Operations groups. Assist with maintaining up to date MBR templates and completes improvement projects related to technical writing.

Essential Functions:

Work closely with the Technical Operations PPT Engineers andCommercial departments in the generation and approval ofMBRs.

Generate and develop all master batch records used in Good Manufacturing Practices environment.

Generate labels for Packaging and Processing (as required).

Generate recipes and documents in FTPS (Factory Talk Pharmasuite).

Attend key project team meetings client teleconferences and on-site visits(as required).

Create change controls(asrequired).

Assist Technical Operations and PPT group(as required).

May be required to assist with report generation from Systems Applications and Products (SAP).

Update and maintain MBR templates to comply with current practices in Operations and PPT.

Maintain a safe working environment and reports potential hazards.

Perform alternating or rotating shift work(as required)

REQUIRED QUALIFICATIONS

Education:

College Diploma in Science/Technical related field.

Experience:

Minimum3yearsrelated experience.

Equivalency:

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

Knowledge Skills and Abilities:

Strongwritten and oral communication skills.Must be well organized and detail oriented.Ablity to to lead improvement projects.Knowledge of Good Manufacturing Practices and ability to follow Standard Operating Procedures (SOPs). Ability to work under pressure and meet tight deadlines. Proficiency with Microsoft Office applications.Proficiency with the English Language.

Standards and Expectations:

Followall Environmental Health & Safety Policies and Procedures. Work harmoniously 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 SOPs and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems in order to maintain a smooth and efficient workflow (visual management scheduling systems shared assets). 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 identifies areas for improvement in the execution ofdepartmentprocedures. Communicate risks to timelines of deliverables in a proactive manner. Consistently strives to improve skills and knowledge in pharmaceutical development (an asset).

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: safety glasses safety shoes lab coat gloveshair net beard coversafety apron respiratoroccasionally.

Compensation

The salary range estimated for this position based in Canada is $50800.00$76150.00.

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards OfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues ...