Director, CMC Biologics Job
- Employer
- Merck
- Location
- West Point PA
- Closing date
- Aug 8, 2016
View more
- Sector
- Science, Computer Science and IT, Information Science and Technology, Life Sciences, Cell and Molecular Biology, Microbiology/Virology, Physical Sciences and Engineering, Chemistry, Biochemistry, Doctors, Infectious Disease, Veterinary Medicine, Pharmaceutical, Quality Assurance, Regulatory Affairs, Law
- Organization Type
- Corporate
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Job Details
Director, CMC Biologics-REG002453
Description
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
For this Director role, responsibilities may include, but are not limited to:
- As an individual contributor uses facilitative leadership skills to lead team within CMC Biologics responsible for the preparation of new filing applications and maintenance of chemistry, manufacturing and control (CMC) documentation for worldwide registration.
- Requires continual correspondence and interaction with regulatory agencies and other scientists to support either new or in-line product filings worldwide.
- Maintain working knowledge of current governmental and worldwide requirements for initial registration, re-registration and post-approval changes.
- Assures that filed information on the current manufacturing and testing procedures is kept updated for each product using appropriate departmental systems.
- Ensures consistency in practices, champions best practices and promotes operational excellence
- Leads others in the biopharmaceutical industry and drives regulators to reduce the regulatory burden of bringing new medicines to market and making post approval improvements in CMC Biologics
- Uses breadth and depth of regulatory, scientific, and technical knowledge to inform strategy development and execution by manufacturing, technical and development teams and to ensure quality of all regulatory interactions and submissions
- Supports talent development within team and within department
Qualifications
Education:
- Required:
- Bachelor's OR Masters degree in science
- Preferred:
- Ph.D.
- Degree concentration in Biochemistry, Molecular Biology, Engineering, Microbiology, or Virology
Required:
- At least 10 years of biologics experience within the pharmaceutical industry.
- Experience in Regulatory CMC
- Development, manufacturing or quality assurance experience .
- Prior Biologics License Application (BLA) or Investigational New Drug (IND) experience in a leadership role.
- Demonstrated sound understanding of related fields (e.g., manufacturing, process development, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving.
- Proven experience in critically reviewing detailed scientific information and assessing whether technical arguments are presented clearly and conclusions are adequately supported by data.
- Expected to develop and possess an expert knowledge of Industry Association Whitepapers, HA regulations & guidance documents.
- He/she is expected to utilize the expert knowledge and reputation to influence the content of new Industry Association Whitepapers, HA guidance & regulations.
- Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner.
- Strong listening skills.
- Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
- Must have a proven record of working with and influencing multi-disciplinary teams and external experts and must have demonstrated leadership, communication, problem solving and decision making skills.
- The candidate must be proficient in English; additional language skills are a plus.
- The candidate may be required to travel on a periodic basis.
Preferred :
- At least 10 years of relevant experience in support of biologics
Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.
Search Firm Representatives Please Read Carefully:
Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Visa sponsorship is not available for this position.
For more information about personal rights under Equal Employment Opportunity, visit:
EEOC Poster
EEOC GINA Supplement
Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.
Job: Regulatory Affairs - CMC
Job Title:Dir, Regulatory Affairs-CMC
Primary Location: NA-US-PA-West Point
Other Locations: NA-US-NJ-Kenilworth
Employee Status: Regular
Travel: Yes, 10 % of the Time
Number of Openings: 1
Shift (if applicable): 1st
Company Trade Name:Merck
Description
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
For this Director role, responsibilities may include, but are not limited to:
- As an individual contributor uses facilitative leadership skills to lead team within CMC Biologics responsible for the preparation of new filing applications and maintenance of chemistry, manufacturing and control (CMC) documentation for worldwide registration.
- Requires continual correspondence and interaction with regulatory agencies and other scientists to support either new or in-line product filings worldwide.
- Maintain working knowledge of current governmental and worldwide requirements for initial registration, re-registration and post-approval changes.
- Assures that filed information on the current manufacturing and testing procedures is kept updated for each product using appropriate departmental systems.
- Ensures consistency in practices, champions best practices and promotes operational excellence
- Leads others in the biopharmaceutical industry and drives regulators to reduce the regulatory burden of bringing new medicines to market and making post approval improvements in CMC Biologics
- Uses breadth and depth of regulatory, scientific, and technical knowledge to inform strategy development and execution by manufacturing, technical and development teams and to ensure quality of all regulatory interactions and submissions
- Supports talent development within team and within department
Qualifications
Education:
- Required:
- Bachelor's OR Masters degree in science
- Preferred:
- Ph.D.
- Degree concentration in Biochemistry, Molecular Biology, Engineering, Microbiology, or Virology
Required:
- At least 10 years of biologics experience within the pharmaceutical industry.
- Experience in Regulatory CMC
- Development, manufacturing or quality assurance experience .
- Prior Biologics License Application (BLA) or Investigational New Drug (IND) experience in a leadership role.
- Demonstrated sound understanding of related fields (e.g., manufacturing, process development, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving.
- Proven experience in critically reviewing detailed scientific information and assessing whether technical arguments are presented clearly and conclusions are adequately supported by data.
- Expected to develop and possess an expert knowledge of Industry Association Whitepapers, HA regulations & guidance documents.
- He/she is expected to utilize the expert knowledge and reputation to influence the content of new Industry Association Whitepapers, HA guidance & regulations.
- Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner.
- Strong listening skills.
- Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
- Must have a proven record of working with and influencing multi-disciplinary teams and external experts and must have demonstrated leadership, communication, problem solving and decision making skills.
- The candidate must be proficient in English; additional language skills are a plus.
- The candidate may be required to travel on a periodic basis.
Preferred :
- At least 10 years of relevant experience in support of biologics
Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.
Search Firm Representatives Please Read Carefully:
Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Visa sponsorship is not available for this position.
For more information about personal rights under Equal Employment Opportunity, visit:
EEOC Poster
EEOC GINA Supplement
Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.
Job: Regulatory Affairs - CMC
Job Title:Dir, Regulatory Affairs-CMC
Primary Location: NA-US-PA-West Point
Other Locations: NA-US-NJ-Kenilworth
Employee Status: Regular
Travel: Yes, 10 % of the Time
Number of Openings: 1
Shift (if applicable): 1st
Company Trade Name:Merck
Company
Our vision is to make a difference in the lives of people globally through our innovative medicines, vaccines, biologic therapies, consumer health and animal products. We aspire to be the best healthcare company in the world and are dedicated to providing leading innovations and solutions for tomorrow.
We have made it our mission to provide innovative, distinctive products and services that save and improve lives, satisfy customer needs and to be recognized as a great place to work
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