Process Scientist Jobs

Experience in technology transfer to manufacturing facilities, including CDMOs

Support the development plans and activities for cGMP antibody production and be accountable for resulting project deliverables

Develop and execute downstream processes and their technology transfer to CDMOs

Author and review process descriptions, technical reports, technology transfer documentation, SOPs, batch records, regulatory filings and other documentation as needed

Working knowledge of Project Management or PMP certification is an advantage.

Good knowledge of vaccines/biologics, Quality principles, and GMP.

Demonstrated expertise in upstream processes and process industrialization/ Knowledge of upstream bacterial culture techniques as well as cell and viral growth.

Excellent verbal and technical writing skills.

Generation of protocols and reports for the feasibility studies occurring in BSL3 laboratory.

Coordinating activity in the lab with multiple teams for upstream studies and execution of the pilot runs.

Experience in biosynthesis, fermentation, bioprocess scale-up;

Experience with analytical methods (chromatography, HPLC, GC, MS);

Experience with operation and maintenance of bioreactors;

Develop and execute analytic procedures for product and byproduct identification via assays and chromatography;

Optimize the product and intermediates clean up procedures, assess purity;

Optimize bioreactor conditions, reagents and microorganisms to increase efficiency and yield of fermentation experiments;

12. Knowledge of Good Laboratory Practices and Good Management Practices is an asset.

·M.Sc. in Bioanalytical Chemistry or Biochemistry with minimum 5 years project management, preferably within the CRO industry.

2.Manage both clinical and preclinical studies / projects following SOPs, Study Plans, and GLP.

4.Skilled in plasma and serum and other tissue extraction.

1.Comprehensive and up-to-date knowledge of Bioanalytical Chemistry.

2.Experience running pharmacokinetic studies and analyzing pharmacokinetic data.

· Certified and/or experienced in the supervisory responsibilities under WSIB, OSHA, and First Aid an asset

Strong interpersonal, verbal, and written communication skills

Strong analytical, problem solving, and decision making skills

Team facilitation/leadership skills and commitment to employee development and continuous improvement methodologies

Comprehensive extended Health and Dental Benefits effective day 1

· Very strong knowledge of processing equipment and automation

Prior experience in enzyme engineering, microbiology, x-ray crystallography is preferable, but not required.

Candidate should possess a Doctoral degree and have a strong background in chemical biology or a related area.

Qualified candidates must have at least one first author paper published or accepted in a peer-reviewed journal.

For Current Gilead Employees And Contractors

Post-Doctoral Scientist – Process Development

Conduct UV irradiation of aqueous suspensions of bacteria or nucleic acids

Develop and execute qPCR methods

Conduct critical review of published literature

Plan, execute, and analyze experiments

A minimum of a Bachelor’s degree in related Science/Engineering field

Excellent interpersonal communication skills, with experience preparing scientific documents and delivering scientific presentations, as well as working in team settings

Use extensive knowledge and expertise in mammalian cell culture and assay development to design, conduct, and analyze experiments

Master’s degree with 3-5 years or PhD degree with 0-1 years of relevant experience (academic or industry) needed

Fully responsible for several scientific platforms and technical areas within the mesenchymal cell product portfolio

Serve as an in-house technical expert and scientific resource, responsible for research project planning, timelines, and budget

Facilitate internal collaborations to move a product from research to launch, and participate in interdepartmental communications and collaborations

In depth knowledge in one of these areas is required: metamaterials and plasmonics, flat optics, silicon photonics.

Some of the typical responsibilities will include:

Learning and developing micro and nano-fabrication processes while operating in a Class 100 cleanroom environment.

Characterizing nanostructures and materials in and out of a cleanroom. Collecting and measuring data and developing characterization models.

Learn photonics and nanofabrication physics and apply them to rapidly evolving photonic devices with application in disruptive technologies.

Effectively contribute to early-stage prototyping and intellectual property development.

Excellent organizational, project and time management capabilities.

Developing and optimizing additive formulations in support of polyethylene product development and/or variable cost management.

Compensation will be commensurate with education and experience

M.Sc. or Ph.D. in Chemistry with minimum 1- 4 years of relevant experience.

Related experience in the field of polymer chemistry, plastics processing and/or polymer additives.

Experience with experimental design and statistical analysis.

•Time management and prioritization skills to meet deadlines and targets.

As a Sales Scientist for CARO Analytical Services’ growing laboratory network, your main responsibilities will include:

•Working closely with other teams, including customer service and operations to ensure a positive customer service experience.

•Minimum 3 years of experience in sales or in a science-capacity role.

•Experience working in chemistry, environmental science or technology sector is an asset.

•Excellent people skills, strong business acumen and relationship-building skills.

Knowledge, Experience & Technical Skills Requirement

Directly interact with management teams of innovative clinical-stage pharmaceutical and VC-backed biotech companies from across Canada, US and Europe.

Experience in screening construct design and optimizing protein expression in a drug discovery platform is ideal.

Experience in downstream applications such as structural biology and biophysics will be an asset.

In-depth understanding and hands-on experience in developing, optimizing, and executing platforms suitable for robust protein production for various downstream applications.

Deep knowledge and a demonstrated track record in enzymology and protein biochemistry in various therapeutic areas.

with knowledge in ingredient functionality & commercialization

Minimum: BS in Food Science with 3-5 years of experience

• Anti-Slip / Steel toed shoes are a requirement for this position

Food Industry Manufacturing environment (Preferred in Biscuit Snacking),

Be actively involved in laboratory management including inventory management and supply chain responsibilities

Partner closely to provide manufacturing support to our research, assay development, downstream formulation, and engineering teams to achieve performance requirements.

Manage multiple tasks and changing priorities in a fast-paced environment

Contribute to departmental strategies and provide input on lab requirements and improvements

Sc or post-graduate degree in chemistry, biochemistry, bioengineering, or related field with 2 years of hands on laboratory experience

Experience with execution of experiments in a wet lab preferably in an industry setting

Thorough understanding and hands-on experience of developing downstream processes for use in a cGMP manufacturing environment

Experience in technology transfer to manufacturing facilities, including CDMOs

Experience in leading and managing cross-functional projects is required

Create the development plans for clinical protein production and be accountable for resulting project deliverables

Provide oversight and guidance on downstream processes and their technology transfer to CDMOs

Author and review process descriptions, technical reports, technology transfer documentation, SOPs, batch records, regulatory filings and other documentation as needed

Prior experience working with Google Suite, Principles of Quality by Design, Product LifeCycle Management (PLM) and SAP interface is highly desired

Prior experience in cell culture and/or cell culture media development is an asset

General knowledge of biological raw materials, ISO 9001, ISO 14001 are desired

Experience in contributing to cross-functional projects is required

Nurture collaborations to deliver non conformance investigation reports on time and ensure all non conformance investigation related activities are documented appropriately

Provide technical support towards Media production services and batch record documentation as required

Experience in technology transfer to manufacturing facilities, including CDMOs

Support the development plans for clinical antibody production and be accountable for resulting project deliverables

Develop and execute upstream antibody production processes and their technology transfer to CDMOs

Author and review process descriptions, technical reports, technology transfer documentation, SOPs, batch records, regulatory filings and other documentation as needed

Client management and communication experience.

Project management and Client interaction.

Two years of experience as Study Director and/or Principal Investigator for bioanalysis.

Has extensive knowledge of GLP.

Possess excellent communication, interpersonal and teamwork abilities.

Has extensive knowledge of Microsoft Word and Excel, ThermoFisher Watson LIMS and Sciex Analyst software.

We value our people and our reputation

We are locally dedicated with international scale

We are future focused and challenge the status quo

We foster collaboration in everything we do

We have an empowering culture and hold ourselves accountable