Senior Scientist (Cell Biology)

Job summary

The Senior Scientist is responsible for the development, validation, and transfer of analytical methods for biopharmaceutical products while overseeing laboratory analysts. They also lead technical discussions with clients, manage projects, and ensure compliance with cGMP guidelines and company SOPs.

Job details

Company Description We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Job Description Responsible for method development, validation and transfer of methods used in testing of biopharmaceutical products or raw materials. Responsible for complex decision making and re-evaluation, optimisation and troubleshooting of methodologies as required by clients. Responsible for providing guidance to and overseeing analysts within the Analytical Operations regarding the performance of their activities related to department. Responsible for leading technical discussions with clients and managing small to mid-sized projects to ensure completion in a timely manner to the satisfaction of both SGS and client management. Execute experiments, following the company’s Standard Operating Procedures, Deviations and Change Control programs and cGMP guidelines. Write and Review technical data, documents, SOPs and proposals as required. Assist in the failure investigations within other SGS groups and design investigation protocols and suggest corrective actions. Qualifications Minimum of MSc in a relevant field with 5 years of relevant laboratory work experience required. Ability to independently lead projects for method development, validation and transfer of methods used in testing of biopharmaceutical products or raw materials. handle end to end delievery of projects. Independently perform routine and complex bench, instrumental and data analysis. Experience with he following techniques: Cell culture, ELISA, Flow cytometer, Microplate readers, qPCR & ddPCR Experience working in a GMP lab environment. Complex decision making and evaluation, optimisation and troubleshooting of methodologies as required by clients. Mentoring, guiding and overseeing analysts within the assigned projects. Leading technical discussions with clients and ensure completion in a timely manner to the satisfaction of both SGS and client management Able to work well under pressure during high (peak) work loads and balancing conflicting demands of high volume versus the quality of results. Extended hours and shift work is required. Additional Information Salary Range: $73,500 - $85,000 CAD annually Some Benefit Highlights: 80% coverage Health, Dental and Vision Paid time off RRSP Program Eligibility SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression and Indigenous status, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities, or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. Accommodations are available on request for qualified candidates during each stage of the recruitment process. Please note that candidates applying for Canadian job openings should be authorized to work in Canada. Compensation: CAD 73500 - CAD 85000 - hourly

What you’ll do

The Senior Scientist is responsible for the development, validation, and transfer of analytical methods for biopharmaceutical products while overseeing laboratory analysts. They also lead technical discussions with clients, manage projects, and ensure compliance with cGMP guidelines and company SOPs.

Requirements

Candidates must hold at least a Master of Science degree in a relevant field and possess a minimum of 5 years of laboratory experience. Proficiency in GMP lab environments, project leadership, and complex analytical troubleshooting is essential.

Benefits

• Health insurance
• Dental insurance
• Vision insurance
• Paid time off
• RRSP program

Listed skills

• Quality assurance · Preferred
• Data analysis · Preferred
• Troubleshooting · Preferred
• Project management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Method development
• Method validation
• Biopharmaceutical testing
• GMP lab environment
• Project management
• Data analysis
• Technical writing
• SOP compliance
• Failure investigation
• Mentoring
• Troubleshooting
• Analytical operations
• Change control
• Instrumental analysis
• Quality assurance
• Method Development
• Time Off Management
• Shift Work
• Data Analysis
• Biopharmaceuticals
• Management
• Good Manufacturing Practices
• Change Control
• Decision Making
• Standard Operating Procedure
• Mentorship
• Operations
• Troubleshooting (Problem Solving)
• Investigation
• Balancing (Ledger/Billing)

Job areas

• Science & Research
• Healthcare
• Management & Leadership
• Engineering
• Scientist
• Quality Control Analyst
• Physical and Engineering Science Technicians Not Elsewhere Classified
• Quality Control Analysts
• Life, Physical, and Social Science Technicians, All Other

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