採用
Work Schedule
Second Shift (Afternoons)
Environmental Conditions
Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse
Job Description Summary:
Responsible for reviewing all data, lab notebooks, and completed Certificates of Analysis (C of A) and Stability reports generated in the Laboratory. Verify and confirm the integrity and traceability of all data generated and reported.
This position is M-F 3:00pm-11:30m.
Essential Functions:
-
Review all regular technical documents (e.g., batch testing, stability testing, method development and validation, raw materials and packaging components) and raw data generated in the Laboratory with high quality and deliver within standard time.
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Release Raw Material and Packaging Components in SAP
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Release of Product Certificate of Analysis using applicable LIMS software
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Ensure the test methods, protocols and Standard Operating Procedures (SOPs) have been followed by the scientists/chemists.
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Verify the integrity and traceability of all data generated and reported.
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Follow up with scientist/chemists to ensure that all necessary corrections are corrected in accordance with Good Manufacturing Practices’ standards.
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Notify department supervisor/manager regarding omissions, incomplete testing results or other irregularities.
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Write/Update SOPs and initiate change control when necessary.
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Adhere to assigned schedules and standard times.
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Maintain a safe working environment and report potential hazards.
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Perform alternating or rotating shift work (as required).
REQUIRED QUALIFICATIONSEducation:
Bachelor of Science in Chemistry or related science.
Experience:
Minimum 3 years of previous pharmaceutical analytical development experience.
Equivalency*:*
Equivalent combinations of education, training, and relevant work experience may be considered.
Knowledge, Skills and Abilities:
Basic understanding the common analytical technologies (e.g., High Performance Liquid Chromatography (HPLC), Gas Chromatography, Ultraviolet (UV) spectroscopy, and titration. Knowledge in Empower, LIMS Nugensis and Trackwise software. Excellent written and oral communication skills. Good working knowledge of Good Manufacturing Practices, International Conference of Harmonization (ICH) and United States Food & Drug Administration (FDA) requirements. Strong organizational skills and detail oriented. Ability to meet deadlines and prioritize. 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 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, 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 regular 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, gloves, hair net, beard cover, safety apron, respirator on occasionally.
Compensation
The salary range estimated for this position based in Ontario is $50,800.00–$76,150.00.
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Thermo Fisherについて

Thermo Fisher
PublicThermo Fisher Scientific Inc. is an American life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.
10,001+
従業員数
Waltham
本社所在地
$200B
企業価値
レビュー
3.0
10件のレビュー
ワークライフバランス
3.5
報酬
3.8
企業文化
3.2
キャリア
3.5
経営陣
2.1
45%
友人に勧める
良い点
Good benefits and compensation
Nice people to work with
Learning opportunities and skill development
改善点
Poor management and leadership issues
Disengaged or unsupportive management
Frequent reorganizations and chaos
給与レンジ
2,092件のデータ
Junior/L3
Mid/L4
Junior/L3 · DATA ANALYST
1件のレポート
$130,000
年収総額
基本給
$100,000
ストック
-
ボーナス
-
$130,000
$130,000
面接体験
8件の面接
難易度
3.0
/ 5
期間
14-28週間
内定率
12%
体験
ポジティブ 12%
普 通 63%
ネガティブ 25%
面接プロセス
1
Application Review
2
Recruiter Screen
3
Hiring Manager Interview
4
Panel Interview
5
Final Interview
6
Offer
よくある質問
Technical Knowledge
Behavioral/STAR
Past Experience
Culture Fit
Industry Specific
ニュース&話題
Thermo Fisher Scientific launches Applied Biosystems™ PowerFlex™ Thermal Cycler - BioSpectrum India
BioSpectrum India
News
·
1d ago
Ninety One North America Inc. Makes New Investment in Thermo Fisher Scientific Inc. $TMO - MarketBeat
MarketBeat
News
·
1d ago
Ninety One UK Ltd Has $517.14 Million Stock Position in Thermo Fisher Scientific Inc. $TMO - MarketBeat
MarketBeat
News
·
1d ago
Thermo Fisher Scientific Inc. $TMO Stock Holdings Lifted by Ninety One SA Pty Ltd - MarketBeat
MarketBeat
News
·
1d ago