Senior Scientist

Sgs; Mississauga; On-site; CAD 74,000 - 85,000; Full time

Benefits offered by this job

Health, Dental & Vision

Paid time off

Job summary

SGS is seeking a senior analyst to lead method development, validation and transfer of analytical methods for biopharmaceutical testing. The role requires independent project leadership, mentoring analysts and delivering results under GMP guidelines.

You will execute experiments, review data and communicate with clients, managing small to mid-sized projects to ensure timely completion and compliance in a fast-paced laboratory environment in Mississauga.

Qualifications

• MSc in a relevant field with 5 years of lab experience.
• Ability to independently lead method development, validation and transfer for biopharmaceutical testing.
• Experience with GMP laboratory environments and complex data analysis.

Responsibilities

• Lead method development, validation and transfer for biopharmaceutical testing.
• Oversee analysts and guide projects within Analytical Operations.
• Conduct experiments following SOPs, deviations, Change Control and cGMP guidelines.
• Communicate with clients and manage small to mid-sized projects to deadline.

Skills

Cell culture

ELISA

Flow cytometry

qPCR

ddPCR

Microplate readers

Education

MSc in a relevant field

Job description

• Compensation: CAD 73,500 - CAD 85,000 - hourly

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 formethod 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

• 80% coverage Health, Dental and Vision
• Paid time off

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.

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