Similar posts
Senior QC Scientist - Analytical Method Development
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Senior QC Scientist - Analytical Method Development - Contract - Lexington, MA
天涯社区官网 is seeking a Senior QC Scientist specializing in Analytical Method Development.
Primary Responsibilities:
The successful candidate will transfer and validate next-generation analytical procedures for testing viral vectors, cell banks, and gene therapy products. They will collaborate with external partners and internal teams to support clinical and commercial product pipelines, ensuring compliance with regulatory guidelines.
Skills & Requirements:
- BS in Chemistry/Biochemistry or related science.
- Experience in analytical laboratory settings, particularly with method validation and transfer.
- Understanding of industry testing requirements and standards.
- Excellent time management and organizational skills.
- Ability to work under pressure and manage changing priorities.
- Familiarity with FDA and EMA guidance documents.
Core competencies:
- Computer literacy (MS Word, Excel, and LIMS).
- Good/effective communication and organizational skills with the ability to work well with others and independently.
- Ability to work collaboratively with cross-functional departments.
The Senior QC Scientist - Analytical Method Development's responsibilities will be:
- Transfer and validate analytical methods for cGMP production.
- Author protocols and reports related to QC method transfer and validation.
- Support document generation for application filings.
- Perform statistical analyses during method validation studies.
- Monitor analytical method performance and system suitability.
- Assist with data trending and compile trend reports.
- Present findings to cross-functional teams and communicate solutions.
- Maintain subject matter expertise in gene therapeutic product quality methods.
- Ensure laboratory procedures are current and facilitate updates.
- Complete documentation in line with cGMP standards.
- Maintain QC lab compliance with industry standards.
- Troubleshoot analytical testing methods as needed.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
天涯社区官网 is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
天涯社区官网 Staffing is an equal opportunity employer.
Related jobs
Highly Competitive
Augsburg, Germany
天涯社区官网 is seeking a Sr. Quality Management Research & Discovery Specialist to join a dynamic team in the medical devices sector.
Highly Competitive
Philadelphia, USA
天涯社区官网 is working alongside a pharmaceutical company to recruit for a Quality Assurance Operations Specialist I. This temporary contract position is based in Philadelphia, Pennsylvania.
Highly Competitive
Visp, Schweiz
天涯社区官网 is seeking a dedicated Scientist QC Raw Materials to join a team focused on quality control within the Primary Packaging and Raw Material sector.
US$55 - US$63 per hour + Highly Competitive Salary
Cambridge, USA
天涯社区官网 is seeking a Quality Assurance Specialist to join our team. In this role, you will focus on maintaining quality and regulatory standards within manufacturing processes.
Highly Competitive Salary
Solothurn, Switzerland
天涯社区官网 is seeking a dedicated Materials Planning Specialist to support manufacturing planning for clinical and commercial programs.
Highly Competitive Salary
Philadelphia, USA
天涯社区官网 is seeking a Manufacturing Associate to join our team in Philadelphia.
Highly Competitive
Visp, Switzerland
天涯社区官网 is currently working alongside a contract manufacturing organisation to recruit for a QA Project Leader for Drug Product. This temporary contract position is based in Visp, Switzerland.
Highly Competitive
Bern, Switzerland
天涯社区官网 sucht einen engagierten Qualitätssicherungsspezialisten für unser Team.