Top 19 R&d engineer Jobs in Pittsfield, Ma

Senior Process Engineer
SHARP STERILE MANUFACTURING LLC —Lee, MA
- $90,000 - $140,000 a year
- Full-time
- 3 years
- Ability to lift 50 pounds
- Math
Quick Apply
Senior Formulation Scientist
SHARP STERILE MANUFACTURING LLC —Lee, MA
- $87,000 - $120,000 a year
- Full-time
- 3 years
- Ability to lift 50 pounds
- Math
Quick Apply
14d
Process Engineer
Crane NXT —Dalton, MA
- $80,000 - $112,000 a year
- Full-time
- Engineering
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Process Engineer
Crane Currency —Dalton, MA
- $80,000 - $112,000 a year
- Engineering
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quality Assurance Manager
Minerals Technologies —Adams, MA
- Full-time
- Management
- 5 years
- English
- Disability insurance
- Health insurance
Lead Hardware Engineer
General Dynamics Mission Systems, Inc —Pittsfield, MA
- $142,696 - $158,303 a year
- Full-time
- 6 years
- Master's degree
- Assembly
- Paid parental leave
- Health insurance
Advanced Electrical Power Engineer
General Dynamics Mission Systems, Inc —Pittsfield, MA
- $124,397 - $138,003 a year
- Full-time
- 3 years
- Master's degree
- Assembly
- Paid parental leave
- Health insurance
Technical Architect
Synagex —Pittsfield, MA
- $100,000 - $130,000 a year
- Full-time
- Azure
- Business development
- Mentoring
- Health insurance
- 401(k)
Quick Apply
Obsolescence Refresh Hardware Electrical Lead
General Dynamics Mission Systems, Inc —Pittsfield, MA
- $118,519 - $131,482 a year
- Full-time
- 3 years
- Master's degree
- Continuous improvement
- Paid parental leave
- Health insurance
Project Manager (New Product Development) - X-Ray Optical Systems
XOS —East Greenbush, NY
- $90,000 - $110,000 a year
- Full-time
- Experience equivalent to degree accepted
- In-person
- Senior level
- Health insurance
- Dental insurance
Program Finance Analyst 2
The Charles Stark Draper Laboratory, Inc. —Pittsfield, MA
- $75,000 - $156,000 a year
- Full-time
- Mid-level
- Office
- 3 years
Quick Apply
Electrical Facilities Design Lead
General Dynamics Mission Systems, Inc —Pittsfield, MA
- $124,397 - $138,003 a year
- Full-time
- 3 years
- Master's degree
- Team management
- Paid parental leave
- Health insurance

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Senior Process Engineer
SHARP STERILE MANUFACTURING LLC —Lee, MA
Due diligence on manufacturing process design and risk analysis to ensure operation safety, efficiency and quality. Able to lift up to 50lbs.
$90,000 - $140,000 a year
Quick Apply
Senior Formulation Scientist
SHARP STERILE MANUFACTURING LLC —Lee, MA
Due diligence on manufacturing process design and risk analysis to ensure operation safety, efficiency and quality. Able to lift up to 50lbs.
$87,000 - $120,000 a year
Quick Apply
14d

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Analytical Chemist, R&D
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Associates degree or higher in chemistry or related field is desired. We have a need for a research and development laboratory technician who will assist with…

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r&d engineer jobs near pittsfield, ma

Senior Process Engineer

SHARP STERILE MANUFACTURING LLC -
Lee, MA

Quick Apply

Job Details

Full-time
$90,000 - $140,000 a year

Qualifications

Manufacturing facility experience
Pharmaceutical company experience
Pharmaceutical manufacturing facility experience

Full Job Description

Position Summary

The Senior Process Engineer is responsible for designing, developing, optimizing and troubleshooting manufacturing processes in a manner that meets safety, quality and operational performance expectations. This position provides leadership and creativity in the formulation development, process development and optimization, scale up and manufacturing. The key function of this role is to identify and solve problems in the manufacturing process transfer and scale up, and deliver effective, safe and efficient manufacturing processes for parenteral drug products. The Senior Process Engineer is hands-on, able to handle multiple tasks with sound planning and communication and providing training and support to peers.

Duties and Responsibilities

Analyze organic or inorganic pharmaceutical excipients to determine chemical or physical compatibilities with active drug molecules for the development of stable pharmaceutical product
Evaluate changes in the composition/stability of pharmaceutical products due to changes in variables such as heat, light, or chemical catalysts for quantitative or qualitative analysis
Propose and prepare formulations with different excipients or solvents to conduct experiments and analytical testing at laboratory scale
Propose and develop lyophilization product and process or other complex formulation process such as liposome, TFF and viscous product
Take an active part in scale-up and technology transfer of newly developed products from R&D to manufacturing
Identify and order materials required to perform development and manufacturing
Identify tooling and equipment required to perform development and manufacturing
Create documents for laboratory/manufacturing operations and quality such as master batch records, study protocols, engineering batch record, process characterization reports, standard operating procedures (SOP), etc. Review these documents for their compliance with cGMP and FDA standards
Due diligence on manufacturing process design and risk analysis to ensure operation safety, efficiency and quality
Propose testing procedures for analyzing CQA and coordinate with quality control testing to ensure the quality of finished drug product
Compile and analyze test information to determine process or equipment operating efficiency or to diagnose malfunctions
Analyze in-process and release testing results to design, analyze, and control pharmaceutical manufacturing processes through the measurement of critical process parameters (CPP) which affect the critical quality attributes (CQA) of the pharmaceutical product
Maintain ownership of assigned laboratory instruments to ensure proper working order and troubleshoot malfunctions when needed
Study effects of various manufacturing techniques or packaging configuration on the composition or stability of pharmaceutical product
Develop, improve or customize equipment, formulas, processes or analytical methods to maintain quality of pharmaceutical product
Write technical papers or reports or prepare standards and specifications for processes, facilities, products, or tests
Carry out all job responsibilities in a safe manner
Develop equipment and processes that meet safety codes, policies and guidelines
Provide for the safety and well-being of operators, maintenance, and other personnel
Confer with scientists or engineers to conduct analyses of research projects, interpret test results or develop procedure and standard tests
Other duties as assigned

Regulatory Responsibilities

Conduct business in a responsible manner that complies with all state, FDA, OSHA, EPA, and DEP regulations, or otherwise as applicable
Provide leadership in daily operations, and have employees incorporate these compliance practices into their daily routines

Supervisory Responsibilities

Lead/support validation activities including equipment validation and process validation
Lead problem solving and investigate quality events related to formulation process or batch records
Propose and lead process improvement initiatives to improve operating performance and laboratory safety procedures to ensure compliance with the cGMP and FDA standards
Lead or participate in root cause analysis and quality event investigation such as OOS and deviations
Supervise, mentor and develop team members or relevant personnel across departments

Experience

A minimum of three (3) years of experience in pharmaceutical research and manufacturing

Education

Bachelor’s degree or above in Chemical Engineering, Chemistry, Biology or Pharmaceutical Science

Knowledge, Skills & Abilities

Experience in sterile manufacturing is preferred
Experience in lyophilization and terminal sterilization techniques are a plus
Knowledge of parenteral drug product manufacturing
Proficient with calculation, data analysis, statistics and applied mathematics
Exceptional computer skills including Microsoft Office, Visio or other related software
Excellent writing skills
Attention to detail

Physical Requirements

Ability to sit for prolonged periods of time
Ability to stand for prolonged periods of time
Able to lift up to 50lbs

Quick Apply

Refine Your Search

r&d engineer jobs in pittsfield, ma

Senior Process Engineer

Senior Formulation Scientist

Process Engineer

Process Engineer

Quality Assurance Manager

Lead Hardware Engineer

Advanced Electrical Power Engineer

Technical Architect

Obsolescence Refresh Hardware Electrical Lead

Project Manager (New Product Development) - X-Ray Optical Systems

Program Finance Analyst 2

Electrical Facilities Design Lead

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