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, (
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

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

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: 

FAX : 303-581-0839 

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


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