Posted 1mo ago

Senior Director, Mid-Atlantic CMC (5362)

@ WuXi Biologics
United States
$160k-$274k/yrRemoteFull Time
Responsibilities:Lead CMC projects, Coordinate cross-functional teams, Support regulatory submissions
Requirements Summary:PhD in Biochemistry or related field; 8-20 years pharma/biotech CMC, process development, analytics; strong cross-functional and regulatory experience; fluent English and Chinese; remote work in the United States.
Technical Tools Mentioned:GMP, ICH Guidelines, Regulatory Submissions
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Job Description

Career Opportunities: Senior Director, Mid-Atlantic CMC (5362)

Requisition ID 5362 - Posted  - Work From Home - United States









































 


Job Title – Senior Director, CMC 

Work Location - United States (Remote)

 

 

 

Summary:Opportunity for Director through the Executive level, depending upon experience.  Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting WuXi Biologic’s services at conferences/trade shows

 

Responsibilities:Provide technical and portfolio leadership to support IND and BLA, enabling CMC activities.Collaborate with CMC functional areas to ensure the successful execution of various CMC projects and the delivery of results on time and within budget.Provide strategic thinking and technical guidance for the project teams, in product development and manufacturing strategyLead CMC projects with a good understanding of potential technical challenges and meeting the regulatory requirements and ICH’s guidelinesServe as the center of solution and decision maker for technical issuesCoordinate efforts and facilitate communication to ensure alignment between WuXi Biologics and clientsWork with a high-performance team to ensure the best quality services, IP, and EHS compliance.  Support corporate business development to enhance the current service offering and develop new clients

 

Qualifications: PhD in Biochemistry, Molecular Biology, Biochemical/Chemical Engineering or related discipline.Technical experience at large pharma or biotech companies.Depending upon the titles, a minimum of 8-20 years of relevant pharmaceutical or biotech industry experience in cell line development, CMC process development, analytical sciences, and/or GMP manufacturingDemonstrates good understanding of the pharmaceutical industry and large molecule drug development.Working knowledge and understanding of current regulations and industry trends for large molecule and Antibody-Drug Conjugate (ADC) product development, manufacture, and testingBiologics manufacturing experienceAbility to effectively work across all levels, functions, sites, and companies. Excellent verbal and written communication skills in both English and ChineseCandidate should possess strong and effective project management, problem solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business and operational areas.Experience in writing regulatory documents and submissions and the ability to work on multiple CMC projects at a time.Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred but not required. Must be a self-starter, self-motivated, and highly flexible in this homebased position with about 10%-15% travel.Must be organized and detail-oriented.

 

 

The pay range for this job opportunity ranges from $160,000 - $274,000The job description does not intend to list all the duties and responsibilities assigned to this position. An employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and the company's business needs. The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.










 




































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Requisition ID 5362 - Posted  - Work From Home - United States


Job Title – Senior Director, CMC 

Work Location - United States (Remote)

 

 

 

Summary:Opportunity for Director through the Executive level, depending upon experience.  Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting WuXi Biologic’s services at conferences/trade shows

 

Responsibilities:Provide technical and portfolio leadership to support IND and BLA, enabling CMC activities.Collaborate with CMC functional areas to ensure the successful execution of various CMC projects and the delivery of results on time and within budget.Provide strategic thinking and technical guidance for the project teams, in product development and manufacturing strategyLead CMC projects with a good understanding of potential technical challenges and meeting the regulatory requirements and ICH’s guidelinesServe as the center of solution and decision maker for technical issuesCoordinate efforts and facilitate communication to ensure alignment between WuXi Biologics and clientsWork with a high-performance team to ensure the best quality services, IP, and EHS compliance.  Support corporate business development to enhance the current service offering and develop new clients

 

Qualifications: PhD in Biochemistry, Molecular Biology, Biochemical/Chemical Engineering or related discipline.Technical experience at large pharma or biotech companies.Depending upon the titles, a minimum of 8-20 years of relevant pharmaceutical or biotech industry experience in cell line development, CMC process development, analytical sciences, and/or GMP manufacturingDemonstrates good understanding of the pharmaceutical industry and large molecule drug development.Working knowledge and understanding of current regulations and industry trends for large molecule and Antibody-Drug Conjugate (ADC) product development, manufacture, and testingBiologics manufacturing experienceAbility to effectively work across all levels, functions, sites, and companies. Excellent verbal and written communication skills in both English and ChineseCandidate should possess strong and effective project management, problem solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business and operational areas.Experience in writing regulatory documents and submissions and the ability to work on multiple CMC projects at a time.Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred but not required. Must be a self-starter, self-motivated, and highly flexible in this homebased position with about 10%-15% travel.Must be organized and detail-oriented.

 

 

The pay range for this job opportunity ranges from $160,000 - $274,000The job description does not intend to list all the duties and responsibilities assigned to this position. An employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and the company's business needs. The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.



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Job Title – Senior Director, CMC 

Work Location - United States (Remote)

 

 

 

Summary:Opportunity for Director through the Executive level, depending upon experience.  Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting WuXi Biologic’s services at conferences/trade shows

 

Responsibilities:Provide technical and portfolio leadership to support IND and BLA, enabling CMC activities.Collaborate with CMC functional areas to ensure the successful execution of various CMC projects and the delivery of results on time and within budget.Provide strategic thinking and technical guidance for the project teams, in product development and manufacturing strategyLead CMC projects with a good understanding of potential technical challenges and meeting the regulatory requirements and ICH’s guidelinesServe as the center of solution and decision maker for technical issuesCoordinate efforts and facilitate communication to ensure alignment between WuXi Biologics and clientsWork with a high-performance team to ensure the best quality services, IP, and EHS compliance.  Support corporate business development to enhance the current service offering and develop new clients

 

Qualifications: PhD in Biochemistry, Molecular Biology, Biochemical/Chemical Engineering or related discipline.Technical experience at large pharma or biotech companies.Depending upon the titles, a minimum of 8-20 years of relevant pharmaceutical or biotech industry experience in cell line development, CMC process development, analytical sciences, and/or GMP manufacturingDemonstrates good understanding of the pharmaceutical industry and large molecule drug development.Working knowledge and understanding of current regulations and industry trends for large molecule and Antibody-Drug Conjugate (ADC) product development, manufacture, and testingBiologics manufacturing experienceAbility to effectively work across all levels, functions, sites, and companies. Excellent verbal and written communication skills in both English and ChineseCandidate should possess strong and effective project management, problem solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business and operational areas.Experience in writing regulatory documents and submissions and the ability to work on multiple CMC projects at a time.Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred but not required. Must be a self-starter, self-motivated, and highly flexible in this homebased position with about 10%-15% travel.Must be organized and detail-oriented.

 

 

The pay range for this job opportunity ranges from $160,000 - $274,000The job description does not intend to list all the duties and responsibilities assigned to this position. An employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and the company's business needs. The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.