Jobs in the United States

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Added 40 mins ago
Retail Contingent
Tapestry, Inc.
Hanover, MD
The Sales Support Associate role is an integral part of the store’s overall success and efficiency; demanding direct attention to our brand commitment when servicing our customers. Leaving…
Added 47 mins ago
CR
Seasonal Associate
Carter's Retail Inc.
Pleasanton, CA
- $16 to $18.25 USD / hour
As a Seasonal Associate, you will be the first face of the brand for growing families. You’ll congratulate new parents and grandparents, introduce them to our new baby essentials, help them…
Added 51 mins ago
SM
Estate Planning & Trust Associate
Strauss Malk & Feder LLP
Northbrook, IL
- $135,000 to $175,000 USD / year
Strauss Malk & Feder LLP is seeking a Trusts & Estates associate attorney to join our growing estate planning group. This is an excellent opportunity for an attorney who possesses a…
Added 1 hour ago
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Added 1 hour ago
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VH
Health Technician (Optometry)
Veterans Health Administration
Wenatchee, WA
- $36,409 to $65,599 USD / year
Assists in creating, implementing, and preparing written and oral reports for the completion of continuous or problem focused Process Improvement and Quality Assurance processes.
Added 2 hours ago
VH
Health Technician (Optometry)
Veterans Health Administration
Wenatchee, WA
- $36,409 to $65,599 USD / year
Assists in creating, implementing, and preparing written and oral reports for the completion of continuous or problem focused Process Improvement and Quality Assurance processes.
Added 2 hours ago
VH
Registered Nurse - Associate Chief Nurse of Mental Health
Veterans Health Administration
Prescott, AZ
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As the Associate Chief Nurse of Mental Health, you will provide program management to ensure coordination of care, including oversight of nursing clinical practice, administrative, and…

Cambrex

Manager, Cleaning Validation

Charles City, IA, United States

Apply on careers.cambrex.com About employer

Applications open in a new tab.

Job details

Apply by: Nov 13, 2027
Experience: Minimum 7 years of relevant experience in pharmaceutical, biopharmaceutical, API, chemical, or other regulated manufacturing environments.
Posting language: English
Posted: Nov 13, 2026

Original job description

Responsibilities

Leadership and People Management

Directly supervise, coach, and develop validation professionals and/or contractors supporting cleaning validation activities, as applicable.

Establish priorities, assign work, monitor progress, and ensure cleaning validation commitments are completed safely, compliantly, and on schedule.

Set performance expectations, support employee development, and provide technical guidance and training.

Communicate validation risks, project status, resource needs, and significant compliance or scheduling issues to site leadership.

Promote a culture of safety, accountability, collaboration, technical excellence, and continuous improvement.

Cleaning Validation Program Leadership

Serve as the site subject matter expert for cleaning validation and cleaning verification activities.

Develop, implement, maintain, and continuously improve the site cleaning validation program, policies, procedures, templates, and standards.

Establish scientifically sound, risk-based validation strategies for manufacturing equipment, processes, products, and facilities.

Develop approaches for equipment grouping, product grouping, worst-case selection, sampling strategy, acceptance criteria, clean and dirty hold times, campaign length, and ongoing verification requirements.

Evaluate new products, processes, equipment, cleaning agents, and process changes to determine cleaning validation requirements before GMP implementation.

Ensure cleaning validation activities are integrated with change control, deviation, CAPA, equipment qualification, process validation, and the overall validation lifecycle.

Validation Execution and Documentation

Lead the preparation, execution, review, and approval of cleaning validation master plans, protocols, studies, technical assessments, and final reports.

Ensure validation documentation is accurate, complete, scientifically justified, and compliant with cGMP requirements and Cambrex procedures.

Partner with Analytical Development and Quality Control on analytical methods used to identify and quantify residues from API manufacturing processes.

Establish acceptance limits and sampling plans based on toxicological or health-based exposure limits, product characteristics, process knowledge, equipment design, analytical capability, and regulatory expectations.

Assess manufacturing procedures, equipment configurations, cleaning instructions, analytical methods, and process changes for impact to validated cleaning processes.

Maintain lifecycle documentation and ensure validated status is preserved following equipment, product, process, or cleaning procedure changes.

Technical Leadership and Risk Management

Lead quality risk assessments and gap analyses related to cleaning processes and validation requirements.

Investigate deviations, failures, atypical results, and adverse trends; determine root cause and ensure appropriate corrective and preventive actions are implemented.

Provide technical expertise regarding equipment cleanability, hard-to-clean locations, sampling locations, cleaning parameters, residue limits, process controls, and validation strategy.

Use data and trend analysis to confirm the continued effectiveness and state of control of validated cleaning processes.

Identify opportunities to standardize cleaning approaches, reduce compliance risk, and improve validation efficiency without compromising product quality or patient safety.

Cross-Functional, Regulatory, and Compliance Support

Partner with Manufacturing, Engineering, Quality Assurance, Quality Control, Analytical Development, Process Development, EHS, and Technical Services to execute validation activities.

Provide cleaning validation input for equipment design, modification, commissioning, qualification, technology transfer, new product introduction, and manufacturing process changes.

Support project teams and manufacturing schedules by coordinating validation scope, resources, timelines, and required documentation.

Ensure cleaning validation activities comply with cGMP, data integrity expectations, site procedures, and applicable FDA, ICH, and other regulatory requirements.

Support customer audits and regulatory inspections as the cleaning validation subject matter expert, including presentation of technical rationale and documentation.

Lead or support responses and remediation associated with validation-related audit findings or regulatory observations.

Maintain inspection readiness of cleaning validation records, procedures, and program governance.

Qualifications/Skills

Strong technical knowledge of cleaning validation, cleaning verification, and validation lifecycle management in pharmaceutical or API manufacturing.
Knowledge of cGMP requirements, quality risk management, change control, deviation, CAPA, and data integrity principles.
Understanding of pharmaceutical or chemical equipment cleaning, sampling techniques, residue testing, analytical methods, and health-based exposure limits.
Strong technical writing, protocol development, investigation, root-cause analysis, and problem-solving skills.
Demonstrated project management skills and ability to manage multiple priorities and timelines.
Proven ability to lead cross-functional technical teams and communicate effectively with employees, leaders, customers, and regulatory inspectors.
Strong attention to detail, sound technical judgment, and commitment to documentation quality and compliance.

Education, Experience & Licensing Requirements

Bachelor's degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences, Biology, Engineering, or a related scientific or technical discipline required; advanced degree preferred.
Minimum 7 years of relevant experience in pharmaceutical, biopharmaceutical, API, chemical, or other regulated manufacturing environments.
Minimum 3 years of direct experience with cleaning validation, process validation, equipment validation, or related validation activities, including significant cleaning validation responsibility.
At least 2 years of experience in a leadership, supervisory, technical lead, or project lead role preferred.
Experience authoring and executing validation protocols, reports, risk assessments, investigations, and validation strategies required.
Experience supporting FDA, customer, or other regulatory inspections preferred.
Experience with API or small-molecule pharmaceutical manufacturing strongly preferred.

Physical Demands, Work Environment, and Travel

Work is performed in office, laboratory, warehouse, mechanical, and pharmaceutical manufacturing environments.

Ability to walk, stand, bend, reach, climb stairs and ladders, and move throughout the manufacturing facility.

Ability to wear required personal protective equipment, including safety glasses, safety shoes, protective clothing, hearing protection, and other PPE as required.

Potential exposure to chemicals, solvents, powders, dust, noise, fumes, odors, moving equipment, and varying temperatures.

Ability to work outside normal business hours when needed to support validation execution, manufacturing schedules, shutdowns, investigations, audits, or inspections.

Occasional travel, generally less than 10% of total work time.

Other Duties

Please note that this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee. Duties, responsibilities, and activities may change at any time with or without notice.

All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities.

Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

Cambrex is committed to providing a safe and productive work environment. All offers of employment are contingent on the successful completion of a comprehensive pre-employment screen. The pre-employment screen may consist of several components including but not limited to a drug test, criminal record check, identity verification, reference checks, education and employment verification, and may vary based on federal, state, and local laws. Refusal to submit to testing will result in disqualification of further employment consideration.

All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law.

Apply on careers.cambrex.com About employer

More about this job

Skills

Cleaning
Good manufacturing practices
Leadership
Inspection
Quality assurance
Quality control
Team leadership
Characteristics of products
Risk management
Brush the equipment
Technical writing
Root cause analysis
Problem solving
Project management
Attention to detail
Documentation
Regulatory compliance
Chemical engineering
Pharmaceutical processes
Personal protective equipment
Vulnerable sector check

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Work requirements

Jobs in the United States