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Research Associate

Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe.

ACTIVE

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description Gilead Sciences in Edmonton, Alberta, Canada is seeking a knowledgeable and motivated professional capable of working effectively in a multi-disciplinary team environment. The successful candidate will assume a full-time employment role in the capacity of Senior Research Associate, Process Development in Gilead Alberta’s Manufacturing Science and Technology (MSAT) department. This individual will assist, primarily from lab-based activities, process chemistry activities for pharmaceutical APIs. These activities will include scale-down model development and qualification, process optimization, robustness studies, formal process characterization and risk assessments, and process validation. In addition, this individual will support process technology transfer activities, due diligence, and facility fit assessment for internal and external manufacturing facilities. Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. By joining Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases. Essential Duties and Job Functions: + Plan and safely execute assigned experiments, with increasing independence, which support Manufacturing Science and Technology (MSAT) department activities and project goals. + Make key observations during reaction, work-up and isolation. + Interpret data effectively, draw conclusions, summarize results and communicate to project and leadership teams. + Demonstrate an ability to recognize anomalous or inconsistent results. + Recommend alternatives, research new methods and techniques, and proactively seek out senior personnel to discuss potential solutions to problems. + Provide regular updates (written and verbal) to the project team supervision. + Use strong verbal communication and interpersonal skills to provide insight into the processes used to achieve experimental results. + Work with collaborative communication and problem-solving spirit. Knowledge, Experience and Skills: + Excellent verbal and written communication skills and strong interpersonal collaboration skills. + Strong desire to work in multi-disciplinary teams, learn new skills and proactively solve problems. + Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems. + Familiarity with modern purification and analytical techniques, including HPLC, NMR, mass spec. + Well-versed in job related software (e.g. Chemdraw, Microsoft Word/Excel/PowerPoint) and scientific literature searching tools (SciFinder, Reaxys, etc.). + Familiarity with statistical analysis to evaluate correlations, shifts and trends of chemical processes, and experience of Design of Experiments (DOE) is an asset. + Experience with kinetic studies or process analytical technologies (PAT) is an asset. + Experience with continuous manufacturing is an asset. + Previous experience in manufacturing under GMP is an asset but not required. Minimum Qualifications: + MSc in Organic Chemistry (or related discipline) and 0+ years of experience OR + BSc in Chemistry and 2+ years of experience (Organic Chemistry focused) For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Gilead Sciences, Inc.

Senior Research Associate (Process Chemist)

Scientist

For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description Scientist – Process Development – Edmonton, Alberta Job Responsibilities: Responsible for developing chemical processes for the manufacturing of drug substances Demonstrates technical knowledge, scientific creativity, and collaboration skills in the development and execution of research for the preparation of novel chemical substance Plans, executes and analyzes laboratory experimentation to advance the knowledge of production and quality attributes of drug substances + Proposes alternative chemistry, including new route selection and step optimization + Provides regular updates to supervision and proposes future research directions + In collaboration with senior scientists, develops project strategy for manufacturing of drug substances to support clinical studies and commercialization + May be responsible for the day to day management of project team members and research assignments, including designing and interpreting of experimentation + Prepares and reviews technical documents including research reports, process development reports, and documentation for the manufacturing of chemical substances e.g. Master Batch Records (MBRs) + Collaborates across functional areas including analytical chemistry, quality assurance, and manufacturing to accomplish project goals + Provides technical support for manufacturing processes performed under cGMP in laboratory manufacturing and large-scale manufacturing operations + Ensures that all experimentation is carried out in accordance with appropriate standard operating procedures (SOPs), maintaining quality, safety, and environmental standards Basic Qualifications: + PhD in Organic Chemistry (or related discipline) OR + MSc in Organic Chemistry with 4+ years of industry expereince OR + BSc in Organice Chemistru with 6+ years of industry experience Preferred Qualifications: + PhD in Organic Chemistry (or related discipline) + Experience in planning and executing multi-step synthesis of organic molecules + Experience scaling up synthetic routes and developing safe processes + Familiarity with purification and analytical techniques, including HPLC, LCMS and NMR + Strong desire to work in multi-disciplinary teams, learn new skills and solve problems + Excellent verbal and written communication skills, and strong interpersonal collaboration skills + Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems + Strong organizational and planning skills Scientist – Process Development – Edmonton, Alberta Job Responsibilities: Responsible for developing chemical processes for the manufacturing of drug substances Demonstrates technical knowledge, scientific creativity, and collaboration skills in the development and execution of research for the preparation of novel chemical substance Plans, executes and analyzes laboratory experimentation to advance the knowledge of production and quality attributes of drug substances + Proposes alternative chemistry, including new route selection and step optimization + Provides regular updates to supervision and proposes future research directions + In collaboration with senior scientists, develops project strategy for manufacturing of drug substances to support clinical studies and commercialization + May be responsible for the day to day management of project team members and research assignments, including designing and interpreting of experimentation + Prepares and reviews technical documents including research reports, process development reports, and documentation for the manufacturing of chemical substances e.g. Master Batch Records (MBRs) + Collaborates across functional areas including analytical chemistry, quality assurance, and manufacturing to accomplish project goals + Provides technical support for manufacturing processes performed under cGMP in laboratory manufacturing and large-scale manufacturing operations + Ensures that all experimentation is carried out in accordance with appropriate standard operating procedures (SOPs), maintaining quality, safety, and environmental standards Basic Qualifications: + PhD in Organic Chemistry (or related discipline) OR + MSc in Organic Chemistry with 4+ years of industry expereince OR + BSc in Organice Chemistru with 6+ years of industry experience Preferred Qualifications: + PhD in Organic Chemistry (or related discipline) + Experience in planning and executing multi-step synthesis of organic molecules + Experience scaling up synthetic routes and developing safe processes + Familiarity with purification and analytical techniques, including HPLC, LCMS and NMR + Strong desire to work in multi-disciplinary teams, learn new skills and solve problems + Excellent verbal and written communication skills, and strong interpersonal collaboration skills + Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems + Strong organizational and planning skills People Leader Accountabilities: •Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. •Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose. •Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem. For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Scientist, Process Development

Manage site process safety operations including: + providing training and guidance to process chemistry personnel in hazards evaluation of chemical processes in the laboratory, + acting as process safety SME for other departments across all areas and levels, + providing process safety assessments for active pharmaceutical ingredient (API) manufacturing performed under cGMP including documentation related to batch records and specifications. Responsible for process safety assessments and investigations for the manufacturing of drug substances, including: + use of appropriate methods and techniques (e.g., DSC, ARC, RC1) to support process development activities and other project goals, + interpretation of data and presentation of process hazard evaluation results.

For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description Senior Scientist – Process Safety and Development KEY RESPONSIBILITIES Manage site process safety operations including: + providing training and guidance to process chemistry personnel in hazards evaluation of chemical processes in the laboratory, + acting as process safety SME for other departments across all areas and levels, + providing process safety assessments for active pharmaceutical ingredient (API) manufacturing performed under cGMP including documentation related to batch records and specifications. Additional: + Continue to develop the process safety evaluation system and procedures for the site, and act as a corporate resource on process safety issues. + Participate in the recruitment, selection, management, development, and evaluation of staff. Strong emphasis on developing colleagues, including mentorship of individuals and project teams. FOCUS AREAS Responsible for process safety assessments and investigations for the manufacturing of drug substances, including: + use of appropriate methods and techniques (e.g., DSC, ARC, RC1) to support process development activities and other project goals, + interpretation of data and presentation of process hazard evaluation results. Additional: + Responsible for the continuous improvement of process safety systems on site, and at the corporate level as required, with a particular focus on personnel and process safety. + Maintain alignment with corporate process safety goals, and direct personnel with interpretation of and compliance with process safety requirements. + Maintain full working knowledge of up-to-date, state-of-the art principles and theories, and regulatory guidance, and applying such knowledge to the development of personnel and systems. + Develop, manage, and promote site process safety programs and systems, including development of process safety assessment tools, training programs, and other tools to support site safety culture and performance. QUALIFICATIONS + Ph.D. in chemistry (or related science or engineering) and 2+ years of relevant experience, OR MS/MA in a related scientific discipline with 6+ years’ industry experience; OR BS/BA in a related scientific discipline with 8+ years’ industry experience + Pharmaceutical/fine chemical industry experience in process safety and development is preferred. + Application of sound and scientific judgment to make timely decisions. + Strong collaboration, communication, and writing skills are required. For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Senior Scientist, Process Safety & Development

OTHER

The candidate will join Q-Block Computing Research for the experimental developments of cavity-coupled neutral atom tweezer array for quantum simulation and computation, as well as commercialization research in quantum communication and sensing. Job summary: As a Senior Quantum Scientist, you will collaborate with other team members, design research projects, and manage a small team of researchers.

Salary range: NegotiableJob type: Full timeLocation: On-site (Edmonton, AB & Wetaskiwin, AB)Job Description: Q-Block Computing is seeking a Senior Quantum Scientist to join our innovative team in Canada. This role offers an exciting opportunity to contribute to the development of cutting-edge quantum technologies in sensing, communication, and computation.  The candidate will join Q-Block Computing Research for the experimental developments of cavity-coupled neutral atom tweezer array for quantum simulation and computation, as well as commercialization research in quantum communication and sensing. Job summary: As a Senior Quantum Scientist, you will collaborate with other team members, design research projects, and manage a small team of researchers. Job duty includes the opportunities for project development and grant proposal writing to initiate government-sponsored research programs. Responsibilities<ul><li>Collaborate with cross-functional teams to design and execute complex atomic molecular optical (AMO) physics experiments.</li><li>Lead a small research team, and mentor junior researchers.</li><li>Contribute to a culture of continuous learning and knowledge sharing within the team.</li><li>Analyze data and interpret results to inform engineering decisions and enhance laboratory capabilities.</li><li>Stay updated with the latest research in quantum science and technology.</li><li>Monthly progress reporting and follow best practices in research data management.</li></ul>Qualification<ul><li>PhD in Physics, Engineering, or a related field with a minimum of 4 years of professional experience.</li><li>Proven track record in experimental quantum information science, or related areas, with particular focus on atomic molecular optical physics.</li></ul>Skills<ul><li>Strong attention to detail, authenticity, and a sense of responsibility in all laboratory tasks</li><li>Critical thinking and problem-solving mindset</li><li>Ability to adapt to fast-moving R&D environment</li><li>Strong communication skills and the ability to work collaborative in a dynamic team environment</li></ul>Benefits<ul><li>Extended health care benefits (inc. dental and vision)</li><li>Life insurance</li></ul>Equal Opportunity: Q-Block Computing is an equal opportunity employer. We are committed to treating all employees and applicants for employment with respect and dignity. If you require assistance and/or reasonable accommodation due to a disability during the application or recruiting process, please feel free to notify us.All interested candidates are encouraged to apply.

Q-Block Computing

Senior Quantum Scientist

BreezyHR

The candidate will join Q-Block Computing Research for the experimental developments of cavity-coupled neutral atom tweezer array for quantum simulation and computation, as well as commercialization research in quantum communication and sensing. Job duty includes research progress reports, laboratory design and implementation, as well as the opportunities to further your skills in experimental atomic molecular optical (AMO) physics.

Salary

Salary range: $57,600 - $115,200Job type: Full timeLocation: On-site (Edmonton, AB & Wetaskiwin, AB)Job Description: Q-Block Computing is seeking a Quantum Scientist to join our innovative team in Canada. This role offers an exciting opportunity to contribute to the development of cutting-edge quantum technologies in sensing, communication, and computation.  The candidate will join Q-Block Computing Research for the experimental developments of cavity-coupled neutral atom tweezer array for quantum simulation and computation, as well as commercialization research in quantum communication and sensing. Job summary: As a Quantum Scientist, you will collaborate with other team members and achieve laboratory milestones under the guidance of senior leaders. Job duty includes research progress reports, laboratory design and implementation, as well as the opportunities to further your skills in experimental atomic molecular optical (AMO) physics.Responsibilities<ul><li>Collaborate with cross-functional teams to design and execute complex atomic molecular optical (AMO) physics experiments.</li><li>Contribute to a culture of continuous learning and knowledge sharing within the team.</li><li>Analyze data and interpret results to inform engineering decisions and enhance laboratory capabilities.</li><li>Stay updated with the latest research in quantum science and technology.</li><li>Monthly progress reporting and follow best practices in research data management.</li></ul>Qualification:<ul><li>Masters/PhD in Physics, Engineering, or a related field.</li><li>Experience in experimental quantum information science, or related areas, with a preference on atomic molecular optical physics.</li></ul>Skills<ul><li>Strong attention to detail, authenticity, and a sense of responsibility in all laboratory tasks</li><li>Critical thinking and problem-solving mindset</li><li>Ability to adapt to fast-moving R&D environment</li><li>Strong communication skills and the ability to work collaborative in a dynamic team environment</li></ul>Benefits<ul><li>Extended health care benefits (inc. dental and vision)</li><li>Life insurance</li></ul>Equal Opportunity: Q-Block Computing is an equal opportunity employer. We are committed to treating all employees and applicants for employment with respect and dignity. If you require assistance and/or reasonable accommodation due to a disability during the application or recruiting process, please feel free to notify us.All interested candidates are encouraged to apply.

Quantum Scientist

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Environmental Manager

Given the importance of keeping one another safe it is expected that you comply with our Health, Safety & Environment (HSE) policy at all times as well as client HSE policies when working at client locations. · Collaborate closely with project coordinators, other project managers, project directors, technical leads, engineers, scientists, and technicians.

Are you ready to elevate your career and make a significant impact on a high-profile national program? WSP is seeking a motivated and skilled Project Manager to join our Remediation Program Management (RPM), Upstream team. Your Key Responsibilities: · Collaborate closely with project coordinators, other project managers, project directors, technical leads, engineers, scientists, and technicians. · Develop technical service offers, work plans, and financial proposals. · Prepare tender documents and ensure they meet client expectations. · Interface with clients to ensure their needs are met and measure project progress and quality. · Plan, manage, and control projects to achieve the set technical, financial, and administrative objectives. · Lead field staff, conduct site visits, and ensure compliance with safety and quality standards. · Mentor and train junior staff involved in the projects. · Ensure adherence to the company's health, safety, and quality management requirements. · Analyze and interpret data and review technical reports. What We Are Looking For: · A bachelor's or master's degree in engineering, geology, or another environmental specialty. · At least 5 years of experience in contaminated site assessments. · Strong knowledge of provincial regulations and best practices in environmental assessments and remediations. · The ability to work well under pressure and meet tight deadlines. · Attention to detail and adaptability. · Excellent teamwork skills and the ability to collaborate with colleagues across Canada. · A strong sense of responsibility and autonomy. · Excellent communication and writing skills in English. · A safety-conscious attitude and understanding of health and safety procedures in the workplace. · Fieldwork experience in environmental assessments and/or remediations. · A valid driver's license and the ability to travel from the office to work sites. Join Us and Make a Difference: At WSP, you will have the opportunity to work on exciting projects, collaborate with a dedicated team, and contribute to meaningful environmental solutions. If you are ready to take the next step in your career and make a real impact, apply today! WSP is one of the world's leading professional services firms. Our purpose is to future proof our cities and environments. We have over 65,000 team members across the globe. In Canada, our 12,000+ people are involved in everything from environmental remediation to urban planning, from engineering iconic buildings to designing sustainable transportation networks, from finding new ways to extract essential resources to developing renewable power sources for the future. At WSP : + 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 Please Note: Health and Safety is a core paramount value of WSP. Given the importance of keeping one another safe it is expected that you comply with our Health, Safety & Environment (HSE) policy at all times as well as client HSE policies when working at client locations. Offers of employment for safety-sensitive positions involving fieldwork are contingent upon candidates being able to perform key physical tasks of the job as described in the job posting and interview. This may include the ability to work in a variety of environmental conditions, such as remote or isolated areas, working alone, and in inclement weather (within safe and reasonable limits). WSP welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process. WSP is committed to the principles of employment equity. Only the candidates selected will be contacted. WSP does not accept unsolicited resumes from agencies. For more information please READ THE FULL POLICY. (https://www.wsp.com/en-CA/careers/notice-to-staffing-agencies)

WSP USA

Environmental Scientist and Project Manager

WSP-Parsons Brinckerhoff

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Chemist Jobs in Riviere Qui Barre

Gilead Sciences, Inc.

Gilead Sciences, Inc.

Gilead Sciences, Inc.

Q-Block Computing

Q-Block Computing

WSP USA