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 Process Engineer Cleaning Validation. Job in Wilson, North Carolina, United States in Merck & Co., Inc.. Nelest.com
Home  |  Contact  |  About Us
|   Register  |  Sign In

Senior Process Engineer Cleaning Validation

col-narrow-left   

Job ID:

22228

Location:

Wilson, NC 

Job function:

Engineering
col-narrow-right   

Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Process Engineer Cleaning Validation

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.

The Senior Specialist Engineer for Cleaning Validation is responsible for providing technical support to the Bottle/Blister/Oral Granules Integrated Production Teams in determining best method for providing optimum performance in equipment, systems, documentation, cleaning validation and quality compliance. Also, responsible for process performance support and troubleshooting for products manufactured at MMD-Wilson.

Primary Duties:






-Responsible for the primary cleaning validation support at Merck Wilson. This includes responsibility for cleaning validation assessments, calculations, validations, product contact surface area swab sampling, equipment design, equipment qualification, process demonstration, process validation and ownership of site master cleaning validation plan.
-Responsible for investigating process deviations and authoring process deviation documentation including technical assessments and product disposition to ensure a constant state of compliance in all processes at Merck Wilson.
-Provides technical assistance to packaging operations in the resolution of processing problems for in-line products.
-Provides written scientific justification for proposed changes by conducting literature search, designing and executing experiments, analytically reviewing current and past data, and demonstrating the impact of process changes on product quality, production efficiency, productivity or cleaning validation.
-Provides technical assistance for quality and regulatory activities including site inspections, preparation of technical documents for NDA supplements, FDA observation, and environmental process issues.
-Responsible for completing all process engineering/process development activities with the highest regard for all Merck Divisional policies and Wilson site procedure for safety, quality, and regulatory compliance.
-Provides technical support in critically evaluating quality standard specifications and methods for raw materials and intermediate and final products.










Travel: Yes, 20 % of the Time

Job Requirements:

Qualifications

Education Minimum Requirement:

Required Qualifications:


-B.S. in Chemical/ Mechanical/Electrical Engineering or Pharmaceutical Sciences and a minimum of four years of experience in Pharmaceutical unit operations or Process Design.

OR


-M.S. in Chemical/Mechanical/Electrical Engineering or Pharmaceutical Sciences and a minimum of three years of experience in pharmaceutical unit operations, or process design.


Required Experience and Skills:


-Demonstrated technical writing and analytical skills.
-Proven communication ability.

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:

27895

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 Process Engineer Cleaning Validation

col-narrow-left   

Job ID:

22228

Location:

Wilson, NC 

Job function:

Engineering
col-narrow-right   

Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Senior Process Engineer Cleaning Validation

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.

The Senior Specialist Engineer for Cleaning Validation is responsible for providing technical support to the Bottle/Blister/Oral Granules Integrated Production Teams in determining best method for providing optimum performance in equipment, systems, documentation, cleaning validation and quality compliance. Also, responsible for process performance support and troubleshooting for products manufactured at MMD-Wilson.

Primary Duties:






-Responsible for the primary cleaning validation support at Merck Wilson. This includes responsibility for cleaning validation assessments, calculations, validations, product contact surface area swab sampling, equipment design, equipment qualification, process demonstration, process validation and ownership of site master cleaning validation plan.
-Responsible for investigating process deviations and authoring process deviation documentation including technical assessments and product disposition to ensure a constant state of compliance in all processes at Merck Wilson.
-Provides technical assistance to packaging operations in the resolution of processing problems for in-line products.
-Provides written scientific justification for proposed changes by conducting literature search, designing and executing experiments, analytically reviewing current and past data, and demonstrating the impact of process changes on product quality, production efficiency, productivity or cleaning validation.
-Provides technical assistance for quality and regulatory activities including site inspections, preparation of technical documents for NDA supplements, FDA observation, and environmental process issues.
-Responsible for completing all process engineering/process development activities with the highest regard for all Merck Divisional policies and Wilson site procedure for safety, quality, and regulatory compliance.
-Provides technical support in critically evaluating quality standard specifications and methods for raw materials and intermediate and final products.










Travel: Yes, 20 % of the Time

Job Requirements:

Qualifications

Education Minimum Requirement:

Required Qualifications:


-B.S. in Chemical/ Mechanical/Electrical Engineering or Pharmaceutical Sciences and a minimum of four years of experience in Pharmaceutical unit operations or Process Design.

OR


-M.S. in Chemical/Mechanical/Electrical Engineering or Pharmaceutical Sciences and a minimum of three years of experience in pharmaceutical unit operations, or process design.


Required Experience and Skills:


-Demonstrated technical writing and analytical skills.
-Proven communication ability.

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:

27895
Copyright © 2016 NELEST.COM All rights reserved