Sr. Scientist I, Bioassay Development
Pharmaron
Summary
The Senior Scientist I will work as part of a team in a laboratory environment to complete client/Sponsor driven projects.
Job description
Key Responsibilities
- Leading Development and Validation of new assays including GxP assays.
- Serving as Principal Investigator (PI) for multiple projects as assigned.
- Contributing to study design, execution, and troubleshooting of projects both internally and in collaboration with clients.
- Acting as Technical and administrative lead for studies, reviewing all documentation related to study execution.
- Authoring and reviewing Protocols, Reports, Deviations, and Audit responses.
- Mentoring and training scientists on techniques and assays.
- Supervising up to three direct reports.
- Performing a QC function to review data and reports to ensure the accuracy of all laboratory-related processes.
- Maintaining regular communication with QAU, scientists, PIs, and other project staff as well as external clients.
- Adhering to all laboratory standards as defined in each written SOP.
- Additional duties and responsibilities as required.
What We're Looking For
- BS in a scientific field with 4 to 6 years of relevant experience, MS with 2-4 years of relevant experience, or PhD with at least 1 year of relevant experience.
- Experience with immunoassays and cell based assay techniques is critical.
- Strong experience with GLP and cGMP as well as assay development and validation is required.
- Must be detail oriented with the ability to multi-task and work as part of a team to complete projects.
- Strong oral and written communication skills and the ability to work without the supervision in a team environment.
- Will participate in client meetings.
- Excellent computer skills are required.
- Must be proficient in Microsoft Office including Word, Excel (formulas, graphs and charts), and PowerPoint.
Requirements
- BS in a scientific field with 4 to 6 years of relevant experience, MS with 2-4 years of relevant experience, or PhD with at least 1 year of relevant experience.
- Experience with immunoassays and cell based assay techniques is critical.
- Strong experience with GLP and cGMP as well as assay development and validation is required.
- Must be detail oriented with the ability to multi-task and work as part of a team to complete projects.
- Strong oral and written communication skills and the ability to work without the supervision in a team environment.
- Will participate in client meetings.
- Excellent computer skills are required.
- Must be proficient in Microsoft Office including Word, Excel (formulas, graphs and charts), and PowerPoint.
Benefits
- Medical, Dental & Vision
- 401(k) Matching
- Paid Time Off
- Paid Sick Leave
- Company Holidays
- Health Savings Account
- Flexible Spending Accounts
- Life Insurance
- AD&D Insurance
- Short-term Disability
- Long-term Disability
- Employee Assistance Program
- Fertility Support
- Maternity Resources
Company overview
Pharmaron is a premier global life sciences service provider founded in 2004, offering comprehensive research, development, and manufacturing services throughout the entire drug discovery and development process. As a leading Contract Research Organization (CRO) and Contract Development and Manufacturing Organization (CDMO), Pharmaron provides integrated solutions across multiple therapeutic modalities including small molecules, biologics, and cell and gene therapy (CGT) products. The company's extensive service portfolio encompasses synthetic and medicinal chemistry, biology services, DMPK (drug metabolism and pharmacokinetics), pharmacology, toxicology, radiochemistry, CMC (chemistry, manufacturing, and controls), and clinical development services. With over 10,000 employees worldwide and facilities across China, the United States, and Europe, Pharmaron supports pharmaceutical and biotechnology companies in accelerating their R&D programs from early discovery through commercial manufacturing. The company is publicly listed on both the Shenzhen and Hong Kong stock exchanges and maintains a strong commitment to scientific excellence, regulatory compliance, and technological innovation in the life sciences sector.