Query SELECT `session_id` FROM `user_session_data_storage` WHERE `session_id` = ? : 
Statement could not be executed (HY000 - 145 - Table './db05/user_session_data_storage' is marked as crashed and should be repaired)
Query INSERT INTO `user_session_data_storage` SET `last_activity` = NOW(), `session_id` = ? : 
Statement could not be executed (HY000 - 145 - Table './db05/user_session_data_storage' is marked as crashed and should be repaired)
Senior Specialst, Quality Assurance. Job in West Point, Pennsylvania, United States in Merck & Co., Inc.. Nelest.com
Home  |  Contact  |  About Us
|   Register  |  Sign In

Senior Specialst, Quality Assurance

col-narrow-left   

Job ID:

22202

Location:

West Point, PA 

Job function:

Business Development
col-narrow-right   

Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Specialst, Quality Assurance

Job Description:

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. Description: The Senior Specialist of Quality Systems, Quality Assurance reports to the WP Site Lead Quality System Associate Director. This position is critical to maintaining the clinical supply chain for investigational product. Specifically this position supports clinical investigations, clinical complaints, deviation management, change management records and Corrective Action Preventive Action s (CAPAs) associated with these events. Areas of focus will be to undertake tasks as it relates to complex supply chains and supply types. Additional support may be required for direct responsibility for Global Clinical Supply (GCS) Integrated Process Team (IPT) and process support. Support Trackwise system business owner responsibilities to include, but not be limited to, user management, system/user training, system configuration and user acceptance testing. Responsibilities:
  • Manage, process and approve Investigations, CAPA extension requests and change management records.
  • Review and approve Quality complaints.
  • Support stock recovery activities.
  • Support Audits (Health Authority, Internal, Divisional).
  • Share in the support of the PSQTS system responsibilities owned by the Quality System Team.
Travel: Yes, 5 % of the Time Description Senior Specialst, Quality Assurance-CLI004578 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. Description: The Senior Specialist of Quality Systems, Quality Assurance reports to the WP Site Lead Quality System Associate Director. This position is critical to maintaining the clinical supply chain for investigational product. Specifically this position supports clinical investigations, clinical complaints, deviation management, change management records and Corrective Action Preventive Action s (CAPAs) associated with these events. Areas of focus will be to undertake tasks as it relates to complex supply chains and supply types. Additional support may be required for direct responsibility for Global Clinical Supply (GCS) Integrated Process Team (IPT) and process support. Support Trackwise system business owner responsibilities to include, but not be limited to, user management, system/user training, system configuration and user acceptance testing. Responsibilities:
  • Manage, process and approve Investigations, CAPA extension requests and change management records.
  • Review and approve Quality complaints.
  • Support stock recovery activities.
  • Support Audits (Health Authority, Internal, Divisional).
  • Share in the support of the PSQTS system responsibilities owned by the Quality System Team.

Job Requirements:

Qualifications Education Requirements:
  • Bachelor's Degree, Scientific or Engineering Discipline Major.
Required:
  • Minimum 5 years' experience in Pharmaceutical or related industry.
  • Strong leadership skills for the ability to lead teams of a cross-functional and multi-level nature, including senior management representatives.
  • Excellent verbal and written communication and presentation skills.
  • Computer skills, knowledge and competency in PowerPoint, Excel, and Word.
  • Ability to independently manage multiple priorities and projects.
  • Working knowledge of Good Manufacturing Practices, including EU requirements.
Preferred:
  • Strong knowledge of clinical development areas.
  • Quality Experience.
  • Project Management skills.
  • Knowledge and competency in Trackwise.
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.

Zip Code:

19486

Company Info
Merck & Co., Inc.

Kenilworth, NJ, United States

Phone:
Web Site: merck.com

Company Profile

Company Info


Merck & Co., Inc.
Kenilworth, NJ, United States
Phone:
Web Site: merck.com

Senior Specialst, Quality Assurance

col-narrow-left   

Job ID:

22202

Location:

West Point, PA 

Job function:

Business Development
col-narrow-right   

Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Specialst, Quality Assurance

Job Description:

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. Description: The Senior Specialist of Quality Systems, Quality Assurance reports to the WP Site Lead Quality System Associate Director. This position is critical to maintaining the clinical supply chain for investigational product. Specifically this position supports clinical investigations, clinical complaints, deviation management, change management records and Corrective Action Preventive Action s (CAPAs) associated with these events. Areas of focus will be to undertake tasks as it relates to complex supply chains and supply types. Additional support may be required for direct responsibility for Global Clinical Supply (GCS) Integrated Process Team (IPT) and process support. Support Trackwise system business owner responsibilities to include, but not be limited to, user management, system/user training, system configuration and user acceptance testing. Responsibilities:
  • Manage, process and approve Investigations, CAPA extension requests and change management records.
  • Review and approve Quality complaints.
  • Support stock recovery activities.
  • Support Audits (Health Authority, Internal, Divisional).
  • Share in the support of the PSQTS system responsibilities owned by the Quality System Team.
Travel: Yes, 5 % of the Time Description Senior Specialst, Quality Assurance-CLI004578 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. Description: The Senior Specialist of Quality Systems, Quality Assurance reports to the WP Site Lead Quality System Associate Director. This position is critical to maintaining the clinical supply chain for investigational product. Specifically this position supports clinical investigations, clinical complaints, deviation management, change management records and Corrective Action Preventive Action s (CAPAs) associated with these events. Areas of focus will be to undertake tasks as it relates to complex supply chains and supply types. Additional support may be required for direct responsibility for Global Clinical Supply (GCS) Integrated Process Team (IPT) and process support. Support Trackwise system business owner responsibilities to include, but not be limited to, user management, system/user training, system configuration and user acceptance testing. Responsibilities:
  • Manage, process and approve Investigations, CAPA extension requests and change management records.
  • Review and approve Quality complaints.
  • Support stock recovery activities.
  • Support Audits (Health Authority, Internal, Divisional).
  • Share in the support of the PSQTS system responsibilities owned by the Quality System Team.

Job Requirements:

Qualifications Education Requirements:
  • Bachelor's Degree, Scientific or Engineering Discipline Major.
Required:
  • Minimum 5 years' experience in Pharmaceutical or related industry.
  • Strong leadership skills for the ability to lead teams of a cross-functional and multi-level nature, including senior management representatives.
  • Excellent verbal and written communication and presentation skills.
  • Computer skills, knowledge and competency in PowerPoint, Excel, and Word.
  • Ability to independently manage multiple priorities and projects.
  • Working knowledge of Good Manufacturing Practices, including EU requirements.
Preferred:
  • Strong knowledge of clinical development areas.
  • Quality Experience.
  • Project Management skills.
  • Knowledge and competency in Trackwise.
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.

Zip Code:

19486
Copyright © 2016 NELEST.COM All rights reserved