Bell International Laboratories
Validation Engineering Specialist
Bell International Laboratories, Eagan, Minnesota, United States
The Validation Engineering Specialist is responsible for the execution of qualification and validation activities at Bell International Laboratories, with a focus on Over-the-Counter (OTC) products, including sunscreens and skincare formulations. The role requires a strong technical and quality background in the pharmaceutical and/or personal care industry. The successful candidate will work cross-functionally with Quality Assurance, Quality Control, and Production teams to support new and ongoing validation initiatives.
Responsibilities
Perform Facility, Utility, and Equipment Qualifications.
Assist in executing Performance Qualifications and Process Validations.
Support the implementation and documentation of Cleaning Validation activities.
Conduct Computer System Validations.
Assist with updating SOPs and participate in training sessions as needed.
Aid Process Engineering, Quality Assurance, Production, and other SMEs in the development and execution of pFMEAs.
Aid other departments in process trials, validation runs, and pilot batches to establish reliable manufacturing processes for new formulations.
Execute validation projects as assigned, ensuring on-time completion.
Prepare and present technical reports, project updates, and validation metrics to senior management.
Ensure qualification and validation processes comply with regulatory requirements (e.g., FDA, OTC monographs) and internal quality standards.
Support quality assurance initiatives by conducting risk assessments, participating in audits, and implementing corrective actions as necessary.Provide technical support for the selection, installation, and qualification of manufacturing equipment and for the development process related documentation (i.e. batch records).
Requirements Required Skills/Abilities
Background in the pharmaceutical industry.
Familiarity with industry best practices for risk assessment.
Knowledge of Facility, Utility and Equipment Qualification requirements.
Understanding of Process Performance Qualification and Process Validation requirements.
Working knowledge of Computer System Validation Requirements.
Working knowledge of Cleaning Validation Requirements.
Strong technical and/or regulatory expertise.
Detailed record keeping and communication of results to others.
Project skills appropriate for leadership of validation projects.
Excellent written, verbal, and interpersonal communication skills.
High level of initiative, innovation, critical thinking, and problem-solving skills
Ability to work cross-functionally & at all levels within the organization including senior leadership.
Ability to prioritize multiple responsibilities and manage deadlines accordingly.
Communicate effectively and professionally both internally and externally.
Exceptional attention to detail and high level of accuracy & organization.
Ability to work as part of a team and excel independently in fast-paced environment.
Ability to adapt quickly to changing circumstances.
Demonstrated leadership skills.
Proficient with Microsoft Office.
RequiredEducation and Experience
Bachelor’s degree in chemistry or other physical science or a related field.
Minimum of 3+ years of experience in pharmaceutical and/or personal care validation, with at least 1 year in Rx or OTC manufacturing.
Demonstrated expertise in the development, execution, and maintenance of validation systems.
Strong knowledge of cGMP, FDA regulations, and OTC compliance standards.
Preferred Education and Experience
Lean Six Sigma Certification (Green Belt or higher) is a plus.
Physical Demands
Regular standing, walking, reaching, and handling of materials and equipment.
Frequent lifting and moving of objects weighing up to 30 pounds.
Occasional bending, crouching, stooping, and kneeling.
Repetitive hand, finger, and arm motions.
The ability to wear required Personal Protective Equipment (PPE).
Visual acuity to inspect product quality and packaging.
Exposure to manufacturing noise, temperature variations, and materials.
Additional Information EEO Statement Bell International Laboratories provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
$67k/yr – $90k/yr Full Time Onsite Monday-Friday Eagan, MN
Health Dental Vision Long Term Disability Life Insurance Critical Care Insurance Accident Insurance PTO Sick Leave Parental Leave 401(k)
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Responsibilities
Perform Facility, Utility, and Equipment Qualifications.
Assist in executing Performance Qualifications and Process Validations.
Support the implementation and documentation of Cleaning Validation activities.
Conduct Computer System Validations.
Assist with updating SOPs and participate in training sessions as needed.
Aid Process Engineering, Quality Assurance, Production, and other SMEs in the development and execution of pFMEAs.
Aid other departments in process trials, validation runs, and pilot batches to establish reliable manufacturing processes for new formulations.
Execute validation projects as assigned, ensuring on-time completion.
Prepare and present technical reports, project updates, and validation metrics to senior management.
Ensure qualification and validation processes comply with regulatory requirements (e.g., FDA, OTC monographs) and internal quality standards.
Support quality assurance initiatives by conducting risk assessments, participating in audits, and implementing corrective actions as necessary.Provide technical support for the selection, installation, and qualification of manufacturing equipment and for the development process related documentation (i.e. batch records).
Requirements Required Skills/Abilities
Background in the pharmaceutical industry.
Familiarity with industry best practices for risk assessment.
Knowledge of Facility, Utility and Equipment Qualification requirements.
Understanding of Process Performance Qualification and Process Validation requirements.
Working knowledge of Computer System Validation Requirements.
Working knowledge of Cleaning Validation Requirements.
Strong technical and/or regulatory expertise.
Detailed record keeping and communication of results to others.
Project skills appropriate for leadership of validation projects.
Excellent written, verbal, and interpersonal communication skills.
High level of initiative, innovation, critical thinking, and problem-solving skills
Ability to work cross-functionally & at all levels within the organization including senior leadership.
Ability to prioritize multiple responsibilities and manage deadlines accordingly.
Communicate effectively and professionally both internally and externally.
Exceptional attention to detail and high level of accuracy & organization.
Ability to work as part of a team and excel independently in fast-paced environment.
Ability to adapt quickly to changing circumstances.
Demonstrated leadership skills.
Proficient with Microsoft Office.
RequiredEducation and Experience
Bachelor’s degree in chemistry or other physical science or a related field.
Minimum of 3+ years of experience in pharmaceutical and/or personal care validation, with at least 1 year in Rx or OTC manufacturing.
Demonstrated expertise in the development, execution, and maintenance of validation systems.
Strong knowledge of cGMP, FDA regulations, and OTC compliance standards.
Preferred Education and Experience
Lean Six Sigma Certification (Green Belt or higher) is a plus.
Physical Demands
Regular standing, walking, reaching, and handling of materials and equipment.
Frequent lifting and moving of objects weighing up to 30 pounds.
Occasional bending, crouching, stooping, and kneeling.
Repetitive hand, finger, and arm motions.
The ability to wear required Personal Protective Equipment (PPE).
Visual acuity to inspect product quality and packaging.
Exposure to manufacturing noise, temperature variations, and materials.
Additional Information EEO Statement Bell International Laboratories provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
$67k/yr – $90k/yr Full Time Onsite Monday-Friday Eagan, MN
Health Dental Vision Long Term Disability Life Insurance Critical Care Insurance Accident Insurance PTO Sick Leave Parental Leave 401(k)
#J-18808-Ljbffr