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Business Process Manager
1201 North Kinzie Avenue Kankakee, IL 60915 US
Job Description
*Depending on experience
The Process Owner will lead key process transformation, design, and improvement efforts across three distinct equipment-related projects at Kankakee site. This role requires close collaboration with Manufacturing, Quality, and Facilities & Engineering to ensure systems meet internal customer, business, and patient needs. The incumbent will serve as a subject matter expert (SME) and provide coaching, documentation ownership, and compliance support throughout the lifecycle of each project.
Project-Specific Focus Areas
Candidates may be assigned to one or more of the following projects based on expertise:
Lift Systems (Immediate Need)
- Experience with mechanical lifting equipment in biopharma environments
- Emphasis on ergonomics, safety, and GMP compliance
Acrylic Columns (Starts January)
- Familiarity with column design and qualification protocols
- Integration into purification processes
Bulk Chemical Delivery Systems (Major Project)
- Knowledge of bulk chemical handling, piping, and delivery systems
- Experience with acids, bases, and cleaning/passivation agents
In addition to core Process Owner duties, candidates should demonstrate:
URS Development
- Collaborate with design teams to define user requirements
- Align system functionality with operational, safety, and compliance needs
Design Review & Risk Assessment
- Participate in P&ID reviews, HAZOP, FMEA
- Provide feedback on usability and accessibility
Equipment & System Testing Support
- Support FAT, SAT, and CQV activities (IV, OV, IOQ, PQ)
- Report functional gaps or deviations
Training & Operational Readiness
- Contribute to SOP and Work Instruction development
- Support hands-on training and knowledge transfer
System Performance Monitoring & Continuous Improvement
- Identify performance deviations and collaborate on improvements
Compliance & Documentation Review
- Ensure GMP/GDP compliance in documentation
- Support audit and inspection readiness
Qualifications:
- Bachelor’s in Mechanical, Chemical, or Manufacturing Engineering (or equivalent)
- 4+ years of relevant experience with BS; 2+ years with MS
- Prior experience in pharmaceutical manufacturing preferred
- Strong knowledge of GMP, FDA, and regulatory standards
- Proficiency in Microsoft Office and technical writing
- Strong interpersonal and collaboration skills
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
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