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Sr. Process Engineer

Minneapolis, MN

COMPANY DESCRIPTION

Syner-G BioPharma Group and Sequoia Biotech Consulting recently merged in September 2024, uniting two industry leaders to create a new force in life sciences consulting. By combining our expertise in product development, regulatory strategy, quality and compliance and commercial manufacturing, we are positioned to deliver fully integrated solutions across the development continuum. 
 
We are helping to enhance human health. This merger strengthens our ability to accelerate groundbreaking therapies and help clients navigate the complex life sciences landscape with greater agility and confidence. Together, we form a leading life sciences consultancy dedicated to empowering organizations to overcome complex challenges and accelerate the speed to market, scale and quality of life-saving innovations.  

We work across a diverse range of clients and projects, supporting many organizations through the most critical phases of the drug discovery, approval, product development, technology transfer and commercial manufacturing process. We also equip our partners with the tools, knowledge and expertise to streamline operations, enhance quality and ensure compliance. 

Syner-G BioPharma Group was recently honored with BioSpace's prestigious "Best Places to Work" 2025 award, for the second consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation. 

At Syner-G and Sequoia, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact. 

For more information, visit www.Sequoiabiotech.com/ or www.Synergbiopharma.com

 

POSITION OVERVIEW:

We are seeking a Project Engineer with extensive experience in equipment for manufacturing and packaging. This role involves leveraging expertise in project management and process improvements to drive compliance, efficiency, and innovation. The ideal candidate will have a strong understanding of regulatory requirements, technical excellence, and the ability to work cross-functionally to support critical business initiatives, with a particular emphasis on product management.

KEY RESPONSIBILITIES:

(This list is not exhaustive and may be supplemented and changed as necessary.)

  • Maintain and enhance manufacturing and packaging quality systems to ensure compliance with FDA, EMA, and related regulations.
  • Develop and improve standard operating procedures (SOPs), work instructions, and quality documentation related to manufacturing and packaging processes with a focus on lifecycle management.
  • Lead and implement change management strategies for manufacturing and packaging, supporting product lifecycle changes and minimizing operational impact.
  • Manage and review equipment change requests to ensure timely, accurate, and compliant updates.
  • Collaborate with regulatory, quality, and manufacturing teams to evaluate and execute changes, supporting a first-time-right approach.
  • Plan, execute, and oversee manufacturing and packaging projects from concept through implementation, ensuring alignment with product launch timelines and regulatory requirements.
  • Develop project scopes, timelines, and resource plans to ensure seamless coordination with cross-functional teams.
  • Identify project risks and implement risk mitigation strategies including process improvements, supply chain redundancy, and regulatory compliance.
  • Analyze existing manufacturing and packaging workflows, identify opportunities for process improvements, and implement best practices to increase efficiency and reduce risk.
  • Drive continuous improvement initiatives to streamline manufacturing and packaging processes, enhancing compliance, productivity, and cost-effectiveness.
  • Provide technical expertise and troubleshooting support for manufacturing and packaging issues, including root cause analysis and corrective action planning.
  • Support manufacturing operations including support, issue trending, and improvement projects.
  • Ensure that all manufacturing and packaging specifications meet regulatory/process standards.
  • Serve as a key liaison between quality assurance, manufacturing, regulatory affairs, and supply chain to align manufacturing strategies with overall business objectives.
  • Support product launches, updates, and regulatory requirements by coordinating with cross-functional teams to achieve timely and compliant product releases.
  • Act as a product manager for manufacturing and packaging equipment, ensuring that product development aligns with market needs and regulatory standards.
  • Monitor market trends and competitor products to identify opportunities for innovation and improvement in manufacturing and packaging equipment.
  • Develop and maintain product roadmaps, ensuring alignment with business goals and customer needs.
  • Collaborate with marketing and sales teams to develop product positioning and messaging that differentiates our products in the market.

QUALIFICATIONS AND REQUIREMENTS:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the education, experience, skills, knowledge, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.

Education:

  • Bachelor’s degree in Engineering, regulatory affairs, or a related field.

Technical Experience:

  • Minimum of 7-11 years of experience in pharmaceutical manufacturing and packaging, with specific expertise in equipment management.
  • Deep understanding of cGMP, FDA, EMA, and USP guidelines relevant to manufacturing and packaging.
  • Proficiency with quality systems including change control and quality events, proficiency in manufacturing and packaging equipment, and compliance.
  • Demonstrated success in managing multiple projects in parallel.

Knowledge, Skills, and Abilities:

  • Excellent communication skills with the ability to work effectively across departments and influence stakeholders.
  • Strong project management skills, with the ability to manage multiple projects simultaneously.
  • Strong leadership and team management abilities.
  • Detail-oriented with strong analytical and problem-solving capabilities.
  • Ability to work in a fast-paced, dynamic environment.

ESSENTIAL FUNCTIONS:

Physical Demands:

The physical demands described here are representative of the requirements that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reach with hands and arms; talk and listen. The employee is frequently required to walk and sit, as well as to lift and carry objects such as books and files weighing up to 25 pounds. The employee is occasionally required to stand, stoop, or kneel. Specific vision abilities required by this position include close vision and the ability to adjust focus.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job, including moderate noise level, an indoor temperate environment, and light levels that are bright and conducive to minimal eye strain, typical for an office environment.

TOTAL REWARDS PROGRAM:

We define total rewards as compensation, benefits, remote work/flexibility, development, recognition, and our culture with programs that support each of our reward pillars. This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy our generous flexible paid time off program, company-paid holidays, flexible working hours, and fully remote work options for most positions and the ability to work “almost anywhere”. However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India.

COMPENSATION:

Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $125,000.00 yearly in our lowest geographic market up to $156,000.00 yearly in our highest geographic market. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.

Applicants must have current work authorization when accepting a position at Syner-G. Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time.

LEGAL STATEMENT 
 

Syner-G BioPharma Group and Sequoia Biotech Consulting are proud to be an Equal Employment Opportunity and Affirmative Action employers. All employment decisions, including the recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment (if necessary) are made without regard to the employee’s race, color, creed, religion, sex, pregnancy or childbirth, personal appearance, family responsibilities, sexual orientation or preference, gender identity, political affiliation, source of income, place of residence, national or ethnic origin, ancestry, age, marital status, military veteran status, unfavorable discharge from military service, physical or mental disability, or on any other basis prohibited by applicable law. Syner-G BioPharma is an E-Verify employer. 

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