Sr Process Engineer

Ferring Pharmaceuticals Inc.; Lake Hiawatha (NJ); On-site; USD 120,000 - 138,000; Full time

Job summary

An established industry player is seeking a Sr Process Engineer to join their dynamic team. This role involves supporting cross-functional teams in executing complex projects related to pharmaceutical manufacturing equipment. You will ensure compliance with cGMP, support validation activities, and contribute to process improvements. The ideal candidate will have a strong engineering background with a focus on aseptic processing and lyophilization. Join a company that values innovation and offers competitive compensation, flexible benefits, and personal development opportunities.

Benefits

Healthcare

401k with Match

Disability Coverage

Life Insurance

Tuition Reimbursement

Paid Time Off

Holidays

Paid Parental Leave

Qualifications

• 5+ years of engineering experience in pharma or biotech.
• Extensive knowledge of cGMP and industry standards.

Responsibilities

• Ensure compliance with cGMP for all tasks.
• Support design and commissioning of process equipment.

Skills

cGMP Compliance

Troubleshooting Skills

Data Analysis

Communication Skills

Problem-Solving

Education

Bachelor's in Mechanical Engineering

Bachelor's in Chemical Engineering

Bachelor's in Electrical Engineering

Tools

Data Analysis Tools

Automation Interfaces

Quality Systems Software

Job description

Job Description:

As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence fosters an entrepreneurial spirit and a long-term perspective, enabling us to grow and scale while remaining agile and true to our 'people first' philosophy. Built on over 70 years of commitment to science and research, Ferring is relentless in its pursuit of discoveries and therapies to help people build families, stay healthy, and combat disease.

Position Overview:

The Sr Process Engineer will support cross-functional teams in executing complex projects related to pharmaceutical manufacturing equipment. Responsibilities include participation in equipment design, FAT/SAT, capital planning, and integration with site systems. The role ensures compliance with cGMP and site procedures, supports validation activities (IQ/OQ), and contributes to process improvements and investigations. Coordination with vendors, users, and fabricators is essential, along with occasional off-hours support. The individual acts as a subject matter expert for regulatory interactions, supports automation and control systems, and collaborates closely with Quality and Regulatory teams on documentation and change controls.

Responsibilities:

• Ensure full compliance with cGMP requirements and internal procedures for all tasks.
• Support design, fabrication, and commissioning of process equipment, including developing capital plans and executing equipment initiatives.
• Coordinate activities with equipment users and external fabricators.
• Review and provide feedback on design documentation, SOPs, and validation protocols.
• Assist with integration of equipment into site networks and monitoring systems.
• Support validation during IQ and OQ execution.
• Investigate deviations and lead CAPA implementation.
• Provide on-call support during off-hours to ensure production continuity.
• Manage engineering activities and prioritize tasks to meet deadlines, including hands-on support.
• Assist in programming, troubleshooting, and maintaining PLCs and monitoring systems.
• Coordinate on-site activities with vendors and contractors.
• Lead FMEA and risk assessments on equipment.
• Support operations in cleanroom environments and participate in daily meetings.
• Contribute to process improvement initiatives and collaborate on projects and quality issues.
• Serve as SME during audits and inspections.
• Work with QA and Regulatory teams on documentation for submissions and change controls.

Requirements:

• Bachelor's degree in Mechanical, Chemical, or Electrical Engineering.
• At least 5 years of engineering experience in pharma or biotech, focusing on aseptic processing and lyophilization.
• Extensive knowledge of cGMP and industry standards related to pharmaceutical manufacturing and validation.
• Proven troubleshooting skills for complex mechanical and process systems.
• Experience supporting design, commissioning, and maintenance of pharma equipment.
• Strong analytical, problem-solving, and data analysis skills.
• Proficiency with data analysis tools, automation interfaces, and quality systems software.
• Excellent communication and organizational skills.
• Willingness to provide on-call, off-shift, and weekend support.

Physical Requirements:

• Work on-site in manufacturing and cleanroom environments.
• Stand, walk, climb, and access elevated or confined spaces as needed.
• Lift up to 25 pounds and wear PPE as required.
• Tolerance to noise, vibration, and temperature variations.
• Support production or projects during off-hours as needed.

Role based in Parsippany, NJ.

Ferring + You:

We offer competitive compensation, flexible benefits, personal support, and development opportunities. Our culture is welcoming and equitable, reflecting our 'People First' philosophy.

Compensation & Benefits:

The base salary range for this role is $120,000 to $138,000, with additional incentive bonuses based on performance. Benefits include healthcare, 401k with match, disability coverage, life insurance, wellness benefits, tuition reimbursement, paid time off, holidays, and paid parental leave.

Equal Opportunity Statement:

Ferring is an equal opportunity employer, committed to diversity and nondiscrimination. We maintain a drug-free workplace.

Join us to make a difference and be part of a team that values your contributions.