Staff Engineer, MSAT Validation

Work Schedule

Environmental Conditions

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier cleaner and safer. Whether our customers are accelerating life sciences research solving complex analytical challenges improving patient diagnostics and therapies or increasing productivity in their laboratories we are here to support them.

Location/Division Specific Information

Greenville NC

How will you make an impact

The Staff Engineer MSAT Validation supports sterile and aseptic manufacturing by leading validation activities across processes cleaning and media fill (aseptic process simulation) programs. This role helps maintain validated state support compliant manufacturing operations and drive effective science- and risk-based validation strategies.

This position may support one or more validation disciplines based on business needs including process validation cleaning validation and media fill/aseptic process simulation. The role is expected to provide technical leadership on complex validation work while collaborating across functions in a sterile manufacturing environment.

What will you do

• Lead and/or support process validation (PPQ) cleaning validation and media fill (aseptic process simulation) activities for sterile/aseptic manufacturing processes.
• Develop validation strategies for new and existing products processes and cleaning procedures using lifecycle and risk-based approaches.
• Author review and execute validation protocols reports risk assessments and related technical documentation.
• Perform data analysis and technical assessment to support validation conclusions and ongoing maintenance of the validated state.
• Support investigations deviations change controls and CAPAs associated with validation and aseptic manufacturing activities.
• Partner cross-functionally with Manufacturing Quality MS&T/Manufacturing Science and Regulatory teams to deliver validation programs.
• Ensure validation activities align with cGMP and applicable global regulatory expectations including FDA and EMA requirements.
• Support internal and external audits and inspections and contribute to continuous improvement of validation and contamination control strategies.

How will you get here

*Must be Legally authorized to work in the United States without sponsorship.

*Must be able to pass a comprehensive background check to include drug screening.

Education

• Bachelors degree in Engineering Chemistry Life Sciences or a related field.

Experience

• 8 years of experience in pharmaceutical and/or biotechnology validation.
• Experience in sterile/aseptic manufacturing environments (required).
• Strong experience in one or more of the following: process validation/PPQ cleaning validation or media fill/aseptic process simulation.
• Experience with validation lifecycle activities and risk-based approaches.

Knowledge Skills Abilities

• Strong understanding of aseptic processing contamination control and validated-state principles.
• Strong knowledge of cGMP and applicable regulatory requirements and expectations.
• Technical writing and documentation expertise including validation protocols and reports.
• Data analysis technical assessment and problem-solving skills.
• Ability to lead complex validation projects independently and manage multiple priorities.
• Strong cross-functional collaboration communication and stakeholder management skills.
• Ability to support audits inspections investigations deviations change controls and CAPAs.

The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job. They are not a comprehensive list of all the duties and responsibilities associated with it.

Competitive wages & Excellent benefits package

• Review our companysTotal Rewards
• Medical Dental & Vision benefits-effective Day 1
• Paid Time Off & Holidays
• 401K Company Match up to 6%(after 1 year)
• Tuition Reimbursement eligible after 90 days
• Employee Referral Bonus
• Employee Discount Program
• Recognition Program
• Charitable Gift Matching
• Company Paid Parental Leave
• We will provide the vital equipment for your role including: computer monitor keyboard mouse etc.
• We also provide any Personal Protective Equipment you may need including: lab coats safety glasses safety shoes etc.

For more information on our benefits please visit: Experience:

Staff IC