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Validation Engineering Specialist I
3 months ago
Summary:
Provides specialized knowledge and information, which is directly needed to support operations. Completes protocols and reports related to the validation of manufacturing processes, packaging processes and cleaning. Review all finished reports prior to final approval. Ensure documents conform to all ThermoFisher Standard Operating Procedures (SOPs), client requirements and Good Manufacturing Practices.
- Prepare and execute validation protocols (new and existing clients) and write reports.
- Review/verify data and performs statistical analysis.
- Monitor the production scheduling and coordination of validation activities as required.
- Attend client meetings as validation representative.
- Provide technical/validation expertise and support to Quality Operations/Business or Project management/operations/Pharmaceutics and Process Technology (PPT).
- Document review of peer protocols and reports.
- Maintain cleaning program and trending cleaning results.
- Support equipment swabbing.
- Attend client meetings as validation representative (as required).
- Support special projects (as required).
- Maintain a safe working environment and report potential hazards.
- Perform alternating or rotating shifts (if required).
Education:
Minimum post secondary diploma in Chemistry, Engineering, Science or related field.
Experience:
One year related experience in the pharmaceutical industry.
Equivalency:
Equivalent combinations of education, training, and relevant work experience may be considered.
- Strong written and oral skills.
- Detail oriented and organized, with a high degree of accuracy and thoroughness.
- Excellent interpersonal skills, communication and organizational skills.
- Strong judgment, decision making and trouble shooting skills.
- Ability to multi-task, meeting tight deadlines in a fast paced environment.
- Mini-Tab and data analysis knowledge an asset.
- Demonstrated computer proficiency with Microsoft Office programs.
- 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 Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion.
Effectively 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. Model 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:
Position requires ordinary ambulatory skills and physical coordination sufficient to move about lab/lab office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally.
Disclaimer:
This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as a comprehensive statement of work, responsibilities, or requirements. Managers and supervisors may assign other duties as needed. Nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully align with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
