Job Title: Senior Pharmaceutical Engineer
Date Posted: 06-10-2008
Job Location: Massachusetts-Boston North
Job Type: Full Time
Education Level: Bachelors Degree
Work Experience: 7+ to 10 Years
Job Shift: First Shift
Yearly Salary:DOE (Depend on Experience)
Company Name: JM Hyde Consulting, Inc
Contact Information: JM Hyde Consulting,   JM Hyde Consulting, (marilyn.bettinger@jmhyde.com)
Job Description:
Senior Pharmaceutical Engineer 

 

Positions available at JMHC offices located in: North Andover, MA

Date: March 2006

Work Term: Full Time

 

JM Hyde Consulting, Inc., (“JMHC”) has been a leader in providing process design, control
systems, and validation expertise to the pharmaceutical, biopharmaceutical and related biotech
industries since 1993. JMHC provides services on large- and small-scale projects. Services
include process and control systems design, and commissioning and validation support for new
and existing pharmaceutical facilities. 

 

JMHC offers a generous compensation package: 

Competitive Salary 
Flexible Work Environment 
PPO Health Care Plan (100% Company Paid) 
Dental Plan (100% Company Paid) 
Disability Plan (100% Company Paid) 
Flexible Benefits Account 
Matching 401K Retirement Plan (50% match up to the Federal legal limit) 
Travel/Overtime Bonus Program 
Paid Time Off Program (PTO) 


The Senior Pharmaceutical Engineer will be responsible for contributing as needed in any of
the four JMHC expertise areas: process design, control systems, commissioning, and validation;
and have the ability to manage project teams and mentor junior staff. 



We are seeking candidates with experience in these areas: 

 

Process Design: 
Client consultation regarding technical approaches to projects 
PFDs, P&IDs, component data sheets, equipment specification, and O&M manual development
Clean water systems, CIP, SIP, and pharmaceutical process equipment 
 

Control Systems: 
The design, programming, testing and start-up of PLCs, SCADA and HMI interfaces, and
integrated systems 
User, Functional, and Detailed Design Specifications review and development
DCS and Delta V

Commissioning:
Conducting FATs and SATs, and preparation of Turn-over Packages
Start-up of Clean Water Systems, CIP and pharmaceutical process equipment 
CIP Cycle Development

Validation: 
Installation, Operational and Performance Qualification Validation protocols development,
execution and final report preparation
Temperature Mapping and SIP Validation
Qualification data analysis with respect to pre-defined acceptance criteria 
Protocol discrepancies or deviations generation and resolution
Internal quality systems and procedures development and maintenance


 Additional Requirements: 

Strong verbal and written communication skills
Manage project teams and mentor junior staff  
A minimum of 7-12 years’ industry experience related to GMP drug manufacture, process design,
automation, commissioning, or validation 
A BS or higher degree in chemical engineering, or a related engineering or scientific
discipline, or significant related experience 
Strong computer knowledge including Microsoft Office 
A willingness to travel

Please e-mail resume and cover letter of interest to: 

E-mail: careers-co@jmhyde.com 
FAX : 303-581-0839 

Web site: www.jmhyde.com 
Direct applicants only. No recruiters or phone calls, please!

 

EOE
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