Specialist Engineering – Sterile Drug Product ExManfg Techology Job
- Employer
- Merck
- Location
- West Point PA
- Closing date
- Mar 1, 2017
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Job Details
Specialist Engineering – Sterile Drug Product ExManfg Techology-CHE005199
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.
The Global Technical Operations, Biological-Sterile (GTO Bio-Sterile) External Manufacturing organization, is seeking a highly motivated individual to fill an open position in the GTO Bio-Sterile External Manufacturing team to support sterile drug product manufacture at contract manufacturing sites. Our team strives to not only provide technical excellence to our work but to be strong partners, collaborators and leaders within the small and large molecule lines of business at Merck as well as externally to identify and incorporate new and innovative approaches.
The Team is seeking a highly motivated individual to partner with the Operations, Quality, Procurement, and Regulatory groups to provide technical support for the Global Change Control Process across the network and Subject Matter Expertise for initiatives. Incumbent will support multiple CMOs with tactical work and process analysis for sterile processes, formulation, filling, visual inspection and packaging. This will include change control, data analysis, investigation support, on-site support for manufacturing, risk assessments and other initiatives. The incumbent will also support regulator inspections, filings, and tech transfers for sterile drug products. The incumbent will have technical and leadership skills in addition interpersonal and communication skills, as they will be part of high performance teams.
Qualifications
Education:
- Required: Bachelor degree in an Engineering or Science Related field
Required:
- Ability to work effectively across boundaries to build strong collaborative relation with other internal GSTC partner groups, Small and Large Molecule Sites and external partners.
- Demonstrated strategic ability to develop innovative solutions for undefined problems and business processes to meet the needs of key stakeholders and project sponsors.
- A minimum of two (2) years experience in biological/pharmaceutical/chemical manufacturing
- Ability to travel up to 25% depending on site needs or vendor support required.
Preferred:
- Proven analytical and technical problem-solving abilities.
- Ability to work both independently and as a part of a team, using strong collaboration skills.
- Demonstrated effective written and verbal communication skills; ability to influence peers.
- Knowledge of regulatory requirements with regard to raw materials used in vaccine manufacturing.
- Change Execution Management training.
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: Chemical Engineering
Job Title:Spclst, Engineering
Primary Location: NA-US-PA-West Point
Employee Status: Regular
Travel: Yes, 25 % of the Time
Number of Openings: 1
Shift (if applicable): 1st
Hazardous Materials: No
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.
The Global Technical Operations, Biological-Sterile (GTO Bio-Sterile) External Manufacturing organization, is seeking a highly motivated individual to fill an open position in the GTO Bio-Sterile External Manufacturing team to support sterile drug product manufacture at contract manufacturing sites. Our team strives to not only provide technical excellence to our work but to be strong partners, collaborators and leaders within the small and large molecule lines of business at Merck as well as externally to identify and incorporate new and innovative approaches.
The Team is seeking a highly motivated individual to partner with the Operations, Quality, Procurement, and Regulatory groups to provide technical support for the Global Change Control Process across the network and Subject Matter Expertise for initiatives. Incumbent will support multiple CMOs with tactical work and process analysis for sterile processes, formulation, filling, visual inspection and packaging. This will include change control, data analysis, investigation support, on-site support for manufacturing, risk assessments and other initiatives. The incumbent will also support regulator inspections, filings, and tech transfers for sterile drug products. The incumbent will have technical and leadership skills in addition interpersonal and communication skills, as they will be part of high performance teams.
Qualifications
Education:
- Required: Bachelor degree in an Engineering or Science Related field
Required:
- Ability to work effectively across boundaries to build strong collaborative relation with other internal GSTC partner groups, Small and Large Molecule Sites and external partners.
- Demonstrated strategic ability to develop innovative solutions for undefined problems and business processes to meet the needs of key stakeholders and project sponsors.
- A minimum of two (2) years experience in biological/pharmaceutical/chemical manufacturing
- Ability to travel up to 25% depending on site needs or vendor support required.
Preferred:
- Proven analytical and technical problem-solving abilities.
- Ability to work both independently and as a part of a team, using strong collaboration skills.
- Demonstrated effective written and verbal communication skills; ability to influence peers.
- Knowledge of regulatory requirements with regard to raw materials used in vaccine manufacturing.
- Change Execution Management training.
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: Chemical Engineering
Job Title:Spclst, Engineering
Primary Location: NA-US-PA-West Point
Employee Status: Regular
Travel: Yes, 25 % of the Time
Number of Openings: 1
Shift (if applicable): 1st
Hazardous Materials: No
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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