Scientist, Analytical Chemistry

Altasciences

$85K — $102K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS/MS in biological or pharmaceutical sciences with 4+ years experience; PhD with 2+ years post-grad experience preferred.
  • Experience in method development, execution, and scientific report writing.
  • Analytical background with GLP experience preferred.
  • Proficiency in Microsoft Office suite and experience with Empower software is a plus.
  • Strong communication skills to engage diverse audiences.
  • Advanced math skills for data analysis and interpretation.

Responsibilities

  • Perform study work in compliance with GLP regulations and maintain documentation accordingly.
  • Plan and manage timelines for assigned studies effectively.
  • Review analytical data to ensure regulatory compliance and accuracy.
  • Assist clients with inquiries regarding study and assay design.
  • Provide scientific guidance during the validation of methods for preclinical studies.
  • Prepare and modify SOPs as needed and provide support to laboratory staff.
  • Design analytical methods and write study reports based on critical data reviews.

Benefits

  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs
  • Telework options when applicable
  • Training & Development Programs
  • Employee Referral Bonus Program
Full Job Description
About the Role
As an Analytical Chemistry Scientist in the Dose Concentration Analysis (DCA) team, you will provide technical and scientific expertise in the required assay for method development, validation/qualification and execution of analytical projects in support of preclinical/clinical studies. This will require rigorous attention to detail, excellent communication skills and the ability to work effectively on interdisciplinary teams of study directors, quality assurance, and other departmental personnel. Bring your strong schedule and work management skills to perform contracted projects according to the timeline provided and excellent data analysis skills with the ability to critically review data for scientific/technical merit and accuracy. Excellent communication skills for interacting with clients and possible clients will be necessary. Finally, our scientists need the ability to understand and conduct work under appropriate regulatory requirements.

What You'll do Here
  • Perform all study work in compliance with GLP regulations and maintain all related documentation in accordance with SOPs, protocol, and analytical plans
  • Accountable for planning and managing timeline of assigned studies
  • Review analytical data to ensure accuracy, completeness, consistency and regulatory compliance
  • Respond to client inquires as needed to assist in study and assay design
  • Provide scientific guidance and participate in the validation/qualification of new and current methods that are used in support of preclinical/clinical studies
  • Prepare and modify SOPs as needed
  • Provide indirect or direct line support of laboratory staff as assigned
  • Design and execute appropriate analytical methods; critically review data and write study reports
  • Serve as responsible/contributing scientist/principal investigator on GLP studies and as scientific resource for junior staff, peers and study directors
  • Interact with clients through execution of analytical studies and provide on-time communication
  • Work with departmental management to sustain analytical businesses with good science and regulation compliance
  • Maintain all related study work documentation in accordance with standard operating procedures (SOPs), study protocol, and analytical plans
  • Prepare abstracts and posters for presentation at scientific conferences


What You'll Need to Succeed
  • BS/MS in a biological or pharmaceutical science or related field with 4+ years in a related field; PhD and 2+ years relevant post-graduate experience
  • Experience with method development, execution, analysis and writing scientific reports required
  • Analytical background required; GLP experience preferred
  • Intermediate computer skills including Microsoft Office suite
  • English proficiency required to read, write, review, interpret and summarize scientific material
  • Effective communication to diverse groups: clients, vendors, internal and external colleagues
  • Advanced maths skills as required for data analysis, interpretation and graphical presentation skills
  • Remain current with state-of-the-art technology
  • Remain current with regulatory guidance and industry standards related to analysis
  • Multi-tasking and strong organizational and project management skills
  • Experience with Empower software preferred


Work Authorization & Sponsorship

Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.

What We Offer

The pay range estimated for this position is $85,000 - $102,000 annually. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.

Benefits

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:
  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs
  • Telework when applicable.


Altasciences' Incentive Programs Include:
  • Training & Development Programs
  • Employee Referral Bonus Program


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