Requirements
- Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biotechnology Engineering, or a closely related discipline
- At least five years of experience as a process engineer in pharmaceutical, biopharmaceutical, or life sciences manufacturing settings
- Familiarity with Good Manufacturing Practices (GMP) and quality standards applicable to clinical and commercial production
- Proficient in using Microsoft Office applications
- Skilled in identifying and resolving process issues and improving operational efficiency
- Hands-on experience with change control systems, documentation practices, and regulatory requirements
- Strong organizational abilities and effective time management with a track record of meeting deadlines
- Clear and effective communication skills, both written and verbal
- High level of accuracy and follow-through on tasks and projects
- Capable of working autonomously in a fast-changing, evolving work environment
- Proven ability to handle uncertain situations and adapt to changing priorities
- Committed to ongoing professional growth and skill development
- Able to establish collaborative relationships across global teams and departments
Nice to Have
- Experience with Single Use Technology (SUT), particularly in monoclonal antibody (mAb) production processes
- Background in commissioning and operating biopharmaceutical manufacturing facilities
Benefits
- 401K plan with employer matching contributions
- Discretionary profit-sharing program
- Annual bonus opportunity, including sales incentives for eligible roles
- Comprehensive paid time off and holiday schedule, including seasonal shutdowns, sick leave, and volunteer days
- Healthcare coverage including medical, dental, prescription drugs, and vision
- Health Savings Account (HSA) and Flexible Spending Account (FSA) options
- Wellness and work-life balance initiatives
- Long-Term Incentive Program, based on job level and performance
- Life and disability insurance coverage
- Concierge service for employee convenience
- Pet insurance benefits
- Tuition reimbursement for continuing education
- Employee referral bonus program
Compensation
Competitive compensation package including annual bonus and long-term incentives
Work Arrangement
On-site with potential for travel
Team
Global, cross-functional team environment
Required (13)
- Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biotechnology Engineering, or a related field
- Minimum 5 years’ experience as a process engineer in Pharma, Biopharma, and/or Life Science industries in a manufacturing/operations role.
- Knowledge and understanding of Good Manufacturing Practices (GMP) and quality compliance issues related to both clinical and commercial manufacturing.
- Proficiency in Microsoft Office Suite
- Strong troubleshooting and process optimization capabilities
- Experience with change control, documentation, and regulatory compliance
- Strong organizational and time management skills with the ability to meet deadlines
- Excellent written and verbal communication skills
- Strong attention to detail and follow-through
- Ability to work independently and adapt in a dynamic, fast-paced environment
- Demonstrated ability to manage ambiguity and shifting priorities
- Commitment to continuous learning and development
- Ability to build relationships and collaborate across a global organization
Preferred (2)
- Knowledge and experience of Single Use Technology (SUT), preferably in monoclonal antibody (mAb) processing.
- Experience with starting up and operating a biopharma manufacturing facility
Not specified
