Quality Control Assay Development Scientist
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Job Detail
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Job Description
Vector BioMed is a state-of-the-art contract development and manufacturing organization (CDMO) specializing in best-in-class lentiviral vectors. We are looking for a highly motivated and experienced Scientist to join our growing team. Responsibilities include Developing, Qualifying, and Validating Analytical Methods commonly used for-in-process, stability, and release testing of GMP manufactured viral vectors in a QC setting. The ideal candidate will have a strong background in assay development and qualification of methods used to characterize GMP manufactured biologics.
- Responsible for assay development/qualification/validation and generation of reports. Methods may include cell-based assays, molecular assays (PCR), Immunoassays, Flow cytometry, etc.
- Responsible for method transfer from internal and external clients.
- Work collaboratively within a team to achieve QC objectives for timely testing of manufactured products and contribute to, or lead, troubleshooting activities.
- Draft, Review, and Follow written procedures and adhere to good documentation practices.
- Participate as a team member on cross functional teams and be given project assignments to train, develop problem solving, and increase technical expertise.
- Proactively identify and implement changes to business and QC processes that improve efficiency and robustness.
- Adhere to quality standards for job training and ensure GMP compliance.
Qualifications:
- Advanced degree (Master’s or Ph.D.) in relevant scientific discipline with a minimum of 4 years experience with Assay Development/Qualification and method transfer supporting cGMP operations in biotech / life sciences (Position title commensurate with experience).
- Experience with mammalian cell culture, aseptic technique, Molecular Biology (digital PCR, sequencing, etc.), Flow Cytometry, Immunoassays; Bioinformatics experience is a plus
- Experience writing and performing method qualification/validation protocols, data analysis, performing method transfer, and writing method qualification/validation reports; experience in cell and gene therapy is a plus.
- Direct experience in the following activities related to Analytical Method Qualification and/or Validation:
- Designing studies
- Drafting and Executing protocols
- Analyzing results to define assay performance characteristics based on regulatory guidance and fit-for-purpose best-practices
- Writing reports
- Excellent communication, interpersonal, and leadership skills, with the ability to collaborate effectively with cross-functional teams and stakeholders at all levels.
- Proven ability to problem-solve, prioritize tasks, and make decisions in a fast-paced and dynamic environment.
- Experience working in GMP environment beneficial.
- Proficiency in statistical data analysis software (e.g., JMP, GraphPad, Minitab, etc.) and Microsoft Office Suite (Word, Excel, PowerPoint, etc.).
Benefits:
- A competitive salary and potential for annual bonus
- Opportunities for learning and growth
- Company-paid holidays and paid time off
- Health, dental, and vision care
- 401K plan
- Short-Term and Long-Term Disability benefits
- Life insurance
- On-site gym
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Application ends in 1d 20h 14min