Clinical-Scientific - Quality Control Chemist - Pioneer Data Systems
Bothell, WA 98021
About the Job
Position Details:
Our client, a world-leading Pharmaceutical Company in Bothell, WA is currently looking for a Method Transfer Lead Scientist to join their expanding team.
Job Title: Method Transfer Lead Scientist / Biologics / REMOTE WORK
Duration: 18 months contract, extendable up to 36 months
Location: Bothell, WA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Position Summary:
Method Transfer Lead (MTL), Scientist, is a QC expert within the Development QC group. This individual contributor has good understanding of analytical method transfer and/or validation to ensure that method transfer and/or validation comply with cGMP and regulatory expectations.
Position Responsibilities:
Support Project Lead for method transfer and/or validation internally and externally for assigned program(s).
Author or review protocols and reports for method transfer and/or method validation or method bridging, and other technical development reports associated with methods.
Plan and track method transfer and/or method validation deliverables.
Collaborate and interact with internal global QC testing sites/labs and external testing sites/labs, project leads and functional reps.
Review method transfer and/or method validation assays, perform data verification, non-routine data mining, and in-depth data analysis
Represent QC in intra-department project/initiative or cross-functional teams in support of program and company goals.
Organizational Relationships:
QC TT team
QCSV-Portfolio
PGS (Pharmaceutical Global Supply)
Analytical R&D
Education And Experience:
Bachelor's degree in life science (Post-graduate degree in a related field is a plus) in biology, biochemistry or any related technical discipline
8 years relevant experience in pharmaceutical/biological drug product development, analytical chemistry and/or QC in a regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required
Technical Skills Requirements:
Expertise in designing and evaluating method validation and transfer studies including approaches such as partial re-validation, co-validation, and cross-validation.
Technical writing skills for authoring methods, validation, and transfer studies/protocols/reports.
Expert knowledge of scientific principles and expertise of mAb, Client, vaccine, gene therapy, able to design and evaluate the design of study/experiment.
Have good mindset and technical skills of analytical methods and plate-based method. Candidate with binding ELISA, cytotoxicity, resProA, res DNA and host cell protein method experiences are preferred but not required.
Good project management skills and experience managing multiple projects at the same time is essential
Possess strong data interpretation, method troubleshooting, skills and sounds scientific judgement
Good time management skills with attention to detail and desire to achieve team and individual goals
Good communication skills to lead a team and influence other leaders or cross-functional team members.
Understand of regulatory guidance and requirements (ICH, CFR, general guidance) pertaining to method transfer and method validation, regulatory submission such as IND, IMPD, BLA or NDA, etc.
Physical Position Requirements:
Non-lab based position.
Hard Skills:
1. Method Transfer Validation in QC
2. Protocols and Reporting
3. Good understanding of analytical and biochemical methodology
Preferred Skills:
1. Binding and Cell based assays
2. more than 8yrs experience
Interview Process:
1st Teams bridge
2nd Panel Teams (Camera On)
Comments:
Non-lab based position.
Open to Fully Remote (prefer Hybrid local to Bothell)
Minimum Education:
Bachelor's degree in life science (Post-graduate degree in a related field is a plus) in biology, biochemistry or any related technical discipline
8 years relevant experience in pharmaceutical/biological drug product development, analytical chemistry and/or QC in a regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required
Our client, a world-leading Pharmaceutical Company in Bothell, WA is currently looking for a Method Transfer Lead Scientist to join their expanding team.
Job Title: Method Transfer Lead Scientist / Biologics / REMOTE WORK
Duration: 18 months contract, extendable up to 36 months
Location: Bothell, WA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Position Summary:
Method Transfer Lead (MTL), Scientist, is a QC expert within the Development QC group. This individual contributor has good understanding of analytical method transfer and/or validation to ensure that method transfer and/or validation comply with cGMP and regulatory expectations.
Position Responsibilities:
Support Project Lead for method transfer and/or validation internally and externally for assigned program(s).
Author or review protocols and reports for method transfer and/or method validation or method bridging, and other technical development reports associated with methods.
Plan and track method transfer and/or method validation deliverables.
Collaborate and interact with internal global QC testing sites/labs and external testing sites/labs, project leads and functional reps.
Review method transfer and/or method validation assays, perform data verification, non-routine data mining, and in-depth data analysis
Represent QC in intra-department project/initiative or cross-functional teams in support of program and company goals.
Organizational Relationships:
QC TT team
QCSV-Portfolio
PGS (Pharmaceutical Global Supply)
Analytical R&D
Education And Experience:
Bachelor's degree in life science (Post-graduate degree in a related field is a plus) in biology, biochemistry or any related technical discipline
8 years relevant experience in pharmaceutical/biological drug product development, analytical chemistry and/or QC in a regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required
Technical Skills Requirements:
Expertise in designing and evaluating method validation and transfer studies including approaches such as partial re-validation, co-validation, and cross-validation.
Technical writing skills for authoring methods, validation, and transfer studies/protocols/reports.
Expert knowledge of scientific principles and expertise of mAb, Client, vaccine, gene therapy, able to design and evaluate the design of study/experiment.
Have good mindset and technical skills of analytical methods and plate-based method. Candidate with binding ELISA, cytotoxicity, resProA, res DNA and host cell protein method experiences are preferred but not required.
Good project management skills and experience managing multiple projects at the same time is essential
Possess strong data interpretation, method troubleshooting, skills and sounds scientific judgement
Good time management skills with attention to detail and desire to achieve team and individual goals
Good communication skills to lead a team and influence other leaders or cross-functional team members.
Understand of regulatory guidance and requirements (ICH, CFR, general guidance) pertaining to method transfer and method validation, regulatory submission such as IND, IMPD, BLA or NDA, etc.
Physical Position Requirements:
Non-lab based position.
Hard Skills:
1. Method Transfer Validation in QC
2. Protocols and Reporting
3. Good understanding of analytical and biochemical methodology
Preferred Skills:
1. Binding and Cell based assays
2. more than 8yrs experience
Interview Process:
1st Teams bridge
2nd Panel Teams (Camera On)
Comments:
Non-lab based position.
Open to Fully Remote (prefer Hybrid local to Bothell)
Minimum Education:
Bachelor's degree in life science (Post-graduate degree in a related field is a plus) in biology, biochemistry or any related technical discipline
8 years relevant experience in pharmaceutical/biological drug product development, analytical chemistry and/or QC in a regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required
Source : Pioneer Data Systems