Production Engineer - Devens MA

VetJobs • Devens, MA

3d • $40 - $49 • Onsite

About The Position

The Production Engineer/Scientist 1 in the Single Use Facility advances the biologics pipeline by following established work instructions and current Good Manufacturing Practices (cGMPs). The role is based in a state-of-the-art facility that uses single-use technology and reports to the Director of Downstream Operations.

The position masters routine manufacturing assignments and provides daily technical oversight of manufacturing processes. It provides in-depth training, supports a culture of compliance and innovation, guides shift personnel in troubleshooting, supports investigations, analyzes process and equipment data, and identifies and implements process improvements.

Requirements

• Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, or Biomedical Engineering) or Life Sciences (Chemistry, Biochemistry, or Microbiology).
• 0 or more years of experience, with no more than 2 years of industry experience.
• Knowledge of science generally attained through a STEM degree.
• Strong academic performance.
• Passion for science and a strong interest in manufacturing operations as a career.
• Fast learner with scientific curiosity, good interpersonal skills, and attention to detail.

Nice To Haves

• Previous pharmaceutical internships or co-op experience and/or university research experience.
• Excellent oral communication skills.
• Demonstrated leadership in professional, school, or community settings.
• Proficiency with common computer tools and web-based applications.
• Prior experience participating successfully on work teams emphasizing personal accountability, attention to detail, collaboration, and results.

Responsibilities

• Master and perform routine manufacturing assignments, including complex assignments requiring initiative to resolve problems and make recommendations.
• Provide in-depth training.
• Use production equipment, process automation, and supporting business systems to support downstream biologics production in accordance with Good Manufacturing Practices and standard operating procedures.
• Ensure less experienced manufacturing personnel comply with SOPs and work instructions, and help ensure their training is completed on time.
• Under area management direction, lead coordination and implementation of special projects such as validation, or support routine process investigations.
• Revise and create process documents.
• Champion area-specific work-safety and operational-improvement initiatives.
• Support continuous improvement by taking ownership of improvements to work processes, equipment, and the safe work environment; advise the Shift Manager on improvements that may optimize processes.
• Guide shift personnel in troubleshooting, support investigations, analyze process and equipment data, and identify and implement process improvements.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level