Process and Package Engineer

Reposted An Hour Ago
Be an Early Applicant
75006, Carrollton, TX, USA
In-Office
Senior level
Beauty • Pharmaceutical • Manufacturing
The Role
Lead and support scale-up of lab formulas to production, plan and execute bulk pilot and fill line trials, specify and evaluate packaging and equipment, create manufacturing and line trial protocols, coordinate cross-functional teams (RID, Operations, Quality), train production staff, and optimize processes for successful, sustainable commercial production runs.
Summary Generated by Built In

Position Summary: The Process and Packaging Engineer will be responsible for seamless and efficient bulk pilot and fill line trials. Function as liaison between RID/Operations/Production to support formula development packaging, bulk and finished goods. This role is responsible for transferring lab formulas from lab to production, developing, and optimizing production processes that efficiently enable successful production run.

Essential Functions, Duties and Responsibilities Other duties may be assigned.

  • Create manufacturing instructions by translating lab processes and observations into practical, scalable production procedures, including batch instructions and support for pilot and line trials.
  • Perform upstream processing and ensure scalability during pilot development.
  • Identify innovative technologies to improve efficiency, enhance quality, and reduce costs for both existing and new products.
  • Lead and support line trials by tracking execution, identifying issues, adjusting processes, and communicating findings to stakeholders.
  • Develop equipment specifications such as fill weight, torque, seal testing, crimping, and commercial run targets in partnership with Quality and Operations.
  • Evaluate packaging suitability and component compatibility while considering equipment capabilities and production readiness.
  • Assess packaging for NPD and changes to existing components, ensuring proper selection for each product.
  • Coordinate packaging components with Operations, RID, and Quality Assurance.
  • Support bulk pilot, first bulk, and fill runs, coordinating batching and filling activities and serving as technical liaison for OTC validation documentation.
  • Create line trial protocols and manufacturing instructions that define clear, product specific process control parameters.
  • Develop process and packaging workflows across all stages of the product lifecycle.
  • Train Compounders and Supervisors on new processes and packaging procedures.
  • Collaborate with RID scientists to ensure formulations meet release specifications and can be successfully scaled and filled.
Qualifications

Skills and Qualifications: 

  • Minimum 5 years of experience in engineering or R&D, ideally within FMCG or related industries.
  • Master’s degree in engineering preferred, or equivalent experience.
  • Experience in CPGs, especially skin care, home, beauty, and personal care technologies; experience with scale up and aerosol products.
  • Process or packaging engineering experience in a GMP environment with OTC products.
  • pFMEA and Lean experience is a plus.
  • Knowledge of bulk processes and packing equipment, including hygienic and sustainability design principles.
  • Experience designing sustainable packaging solutions that balance protection, functionality, and customer experience.
  • Knowledge of innovation management workflows in the personal care industry.
  • Ability to thrive in dynamic environments and adapt approaches as needed.
  • Experience identifying cost effective packaging solutions that meet functional and aesthetic requirements.
  • Strong critical thinking and problem solving skills.
  • Excellent verbal and written communication skills.
  • Demonstrated analytical and critical thinking.
  • Strong project and time management skills with the ability to coordinate multiple workstreams and timelines.

 

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be provided to enable individuals with disabilities to perform essential functions.


Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform 'the essential functions’ of this job.


The employee must regularly lift and /or move up to 25 pounds, frequently lift and/or move up to 50 pounds. While performing the duties of this Job I the employee is regularly required to use hands to finger! handle or feel and reach with hands and arms. The employee is frequently required to stand, sit, and climb or balance. The employee is occasionally required to walk; stoop kneel, crouch, or crawl; talk or hear and taste or smell. The worker is required to have visual acuity to determine the accuracy, neatness, thoroughness of work assigned (i.e., custodial, food services, general labor, etc.}.

 

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.

 

Skills Required

  • Minimum 5 years of experience in a relevant engineering or R&D field
  • Master's degree in engineering or equivalent combination of education and experience
  • Previous experience in CPGs, especially skin care, home, beauty, and personal care product technologies
  • Experience with scale up and aerosol products
  • Proven experience in process or packaging engineering in a GMP environment with OTCs
  • Knowledge of bulk processes/packing equipment principles and hygienic and sustainability design
  • Experience identifying cost-effective packaging solutions that meet functional and aesthetic requirements
  • Knowledge of innovation management workflows in the personal care business
  • Analytical, critical thinking, and effective verbal and written communication skills
  • Project and time management skills to coordinate multiple work streams and timelines
  • Ability to train compounders and supervisors on new processes and packaging procedures
  • Ability to regularly lift/move up to 25 pounds and frequently up to 50 pounds
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The Company
Year Founded: 1988

What We Do

Swiss American CDMO is a full-service Contract Development & Manufacturing Organization (CDMO) that develops and manufactures topical skin and wound care products for global brands. They specialize in creating innovative solutions for cosmetic, OTC drug, and medical device regulatory pathways.

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