Impress employers and recruiters.
Choose from hundreds of resume examples.

Impress employers and recruiters.
Choose from hundreds of resume examples.

Target Resume Now

About the Role

Serves as a technical resource supporting company objectives with respect to engineering design, process, and implementation of chemical process and controls. Projects include manufacturing systems, sterile filing systems, process piping, utility systems, new facility construction and upgrades, and other applications.

Responsibilities

• Engage in technical discussions with potential suppliers
• Organize and write specifications based on needs and requirements
• Launch calls for tenders (Request for Proposal, Request for Service)
• Ensure the solution designed respects established specifications
• Ensure technical choices deviating from specifications are documented and validated
• Execute projects and tasks within approved deadlines and budget
• Work in partnership with external companies
• Propose and apply solutions to mitigate work delays
• Proactively alert site management to potential problems
• Ensure successful commissioning of the project
• Monitor installations and commissioning of equipment
• Coordinate suppliers and vendors, ensuring compliance to health and safety instructions
• Possess adequate technical expertise for problem resolution
• Respect data in specifications
• Communicate with Production to coordinate activities with production constraints
• Assist with commissioning activities and putting equipment into production
• Carry out an assessment after each commissioning
• Serve in an expert role in writing qualification protocols, executing tests, and approving reports
• Participate in operator training
• Work with internal customers to define training requirements and provide technical content
• Organize training in collaboration with suppliers
• Study technical needs associated with new site investments
• Participate in project groups
• Collect and analyze needs from internal stakeholders
• Define technical solutions and implementations
• Respect technical, regulatory, and quality requirements
• Take into account necessary parameters (water production, energy, etc.)
• Respect flows, workshop ergonomics, and safety constraints
• Ensure documentation of completed projects is updated
• Collect technical drawings from vendors for review
• Create technical drawings of the factory and update according to approved documentation practices

Requirements

• Minimum 3 years in either a manufacturing environment, or equipment and packaging technology
• Experience in a regulated environment (FDA) is a plus
• Hands-on experience with small molecule solids and liquids manufacturing equipment is a benefit
• Experience in sterile manufacturing is preferred but not required
• Strong background in technical troubleshooting and problem-solving
• Detailed knowledge of equipment operation and validation requirements
• Ability to work in a matrix organization with cross-functional teams
• Ability to specify, procure, oversee installation, and commission systems and processing equipment
• Strong project management skills
• Proficient knowledge of pharmaceutical cGMP requirements and systems is a plus
• Must be able to work on a computer for extended periods
• Must wear safety glasses and other protective items as required
• Ability to travel for business (Domestic and International)

Skills

• Engineering design
• Process and controls implementation
• Technical troubleshooting
• Problem-solving
• Equipment operation and validation
• Project management
• Pharmaceutical cGMP requirements

Location

• Rochester, NY

Work Type

• Full-time

Experience Level

• Minimum 3 years

Education Level

• Bachelor’s degree in Chemical Engineering or related discipline with equivalent experience
• Master’s Degree considered a plus
• Associate’s degree with highly relevant experience will be considered

Salary/Compensations

• 80,000.00 - 95,000.00 USD

Benefits

• 100% employer-paid medical premiums
• 401(k) contributions: 6% match plus an additional 4% company-funded contribution
• HSA contributions with wellness incentives
• Annual performance bonuses and merit increase eligibility

About the Company

• French pharmaceutical industrial group striving to make healthcare solutions accessible
• World leader in sterile single dose with 10 sites on 4 continents and over 2400 employees
• Unither Manufacturing LLC. in Rochester (NY) specializes in Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules, with over 360 employees
• Dynamic company driven by a spirit of victory, pursuing strong growth while maintaining a close relationship with customers and employees
• Culture based on 5 values: Respect, Responsibility, Trust, Courage and Innovation
• Committed to providing employees with autonomy, encouraging initiatives, and offering working conditions conducive to development and potential expression
• Site values the meaning of work and entrusts employees with a high level of responsibility

Equal Opportunity

• Unither is an Equal Opportunity Employer.
• Committed to providing reasonable accommodations for qualified individuals with disabilities and to ensuring equal employment opportunity for all applicants.