Bioanalytical Scientist LC-MS/MS
Pharmaron
- Pay
- $85K to $93K
- a year
- Location
- Germantown, MD
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 22
- 2 days ago
Career path
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About the company
Pharmaron
Pharmaceuticals · 10,001+ employees
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore . Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
What you'll do
- Collaborate with Lead Scientists to execute LC-MS/MS assay development, validation, and sample analysis activities in accordance with study requirements and applicable regulatory guidance.
- Maintain compliance with laboratory safety policies, company SOPs, and study-specific plans, including completion and self-review of required training documentation and refresher training.
- Support staff training, mentoring, and technical development as needed.
- Oversee assigned laboratory equipment scheduling, maintenance, and calibration.
- Develop and review SOPs and contribute to departmental process improvements.
- Apply knowledge of FDA bioanalytical method validation guidance and applicable regulatory requirements.
- Prepare data tables and reports in Watson™ LIMS and support data transfers and preclinical and clinical data management activities.
- Coordinate procurement of reference materials, control plasma, and study-specific consumables.
- Support responses to Quality Assurance (QA) audit findings.
- Support onboarding and initial training of new hires.
- May serve as a line manager for Associate Bioanalytical Scientists.
- Serve as the primary sponsor contact for assigned studies, leading client communications and providing updates on study progress and deliverables.
- Plan and oversee study execution, including experimental design, data interpretation, and preparation, review, and finalization of study reports.
- Review study-related documents, including laboratory manuals, clinical protocols, and data transfer agreements.
- Coordinate with sample management, report writing, and QA teams to ensure appropriate sample handling, report completion, audit readiness, and resolution of study findings.
- Oversee study documentation and archiving, including correspondence and electronic raw data.
- Provide scientific and technical support for business development activities, including client visits.
- Participate in and present at scientific conferences.
What you need
- BS I: PhD in relevant field with at least 0-1 year of experience, OR Master of Science in relevant field with at least 2-3 years relevant experience, OR Bachelor of Science in relevant field with at least 4 years relevant experience.
- BS II: PhD in relevant field with at least 1-2 year of experience, OR Master of Science in relevant field with at least 3-4 years relevant experience, OR Bachelor of Science in relevant field with at least 5 years relevant experience.
- Education: a bachelor's degree or a postgraduate degree
Key skills
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Perks
- Medical, Dental & Vision Insurance
- 401(k) Retirement Plan
- Paid Time Off
- Paid Sick Leave
- Company Holidays
- Health Savings Account
- Employee Assistance Program
- Professional development
See full description on company page, apply now