Senior Scientist
- Mississauga, ON, Canada
Salary Range: $73,500 - $85,000 CAD annually · Full-time
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Job details
- Pay
- Salary Range: $73,500 - $85,000 CAD annually
- Job type
- Full-time
- Apply by
- Experience
- Minimum of MSc in a relevant field with 5 years of relevant laboratory work experience required.
- Posting language
- English
- Posted
Original job 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.
- 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 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.
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.
More about this job
Responsibilities
Develop, validate, transfer, optimize, and troubleshoot analytical methods for biopharmaceutical products and raw materials, while conducting experiments in accordance with SOPs, cGMP, and related quality systems. Lead projects and client technical discussions, oversee and mentor analysts, prepare and review technical documentation, and support failure investigations and corrective actions.
Requirements
Requires a relevant MSc and at least five years of relevant laboratory experience, including experience in a GMP laboratory. Candidates must be able to independently lead end-to-end method projects, perform complex laboratory and data analysis, guide analysts, manage client discussions, and work under pressure, including extended hours and shift work.
Skills
- Method Development
- Method Validation
- Method Transfer
- Biopharmaceutical Testing
- Raw Material Testing
- GMP Laboratory Practices
- Analytical Operations
- Instrumental Analysis
- Data Analysis
- Troubleshooting
- Project Management
- Client Technical Discussions
- Technical Writing
- Failure Investigation
- Mentoring and Guidance
- cGMP Compliance
Benefits
- Health Coverage
- Dental Coverage
- Vision Coverage
- Paid Time Off
- RRSP Program Eligibility
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Healthcare
- Management & Leadership
- Manufacturing
Keywords
- Biopharmaceutical Products
- Raw Materials
- Method Development
- Method Validation
- Method Transfer
- Analytical Operations
- GMP
- cGMP
- Standard Operating Procedures
- Deviations
- Change Control
- Laboratory Testing
- Bench Analysis
- Instrumental Analysis
- Data Analysis
- Method Optimization
- Troubleshooting
- Project Management
- Client Management
- Technical Documentation
- SOPs
- Proposals
- Failure Investigations
- Investigation Protocols
- Corrective Actions
- Quality of Results
- Analyst Mentoring