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Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Division / Site Information

Pharma Services Group/ Cincinnati, Ohio

With the support of over 800 talented employees, Thermo Fisher Scientific’s oral solid dose (OSD) site in Cincinnati, Ohio offers a range of drug development and commercial manufacturing service

Thermo Fisher Scientific is a global leader in serving science, with revenues of more than $40 billion and approximately 130,000 colleagues worldwide. This role sits within our **Manufacturing Sciences** organization, supporting GMP manufacturing operations for therapeutic and diagnostic products. The position operates in a regulated manufacturing environment where collaboration, technical excellence, and continuous improvement are essential to success.

Discover Impactful Work

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Every day, our colleagues bring our Mission to life—enabling our customers to make the world healthier, cleaner, and safer. In this role, you will work at the critical intersection of research and manufacturing, helping ensure robust, compliant, and scalable processes that support life-changing therapies and diagnostics.

Day in the Life

As a **Manufacturing Sciences Scientist II** , you will play a key role in supporting reliable and compliant manufacturing operations by applying scientific and technical expertise.

Key Responsibilities Include:

+ Support manufacturing operations through process optimization, troubleshooting, and continuous improvement initiatives

+ Participate in technology transfer activities from development into GMP manufacturing

+ Support process validation, scale-up, and ongoing process monitoring efforts

+ Apply scientific principles to investigate deviations, perform root cause analysis, and implement corrective and preventive actions

+ Collaborate with Manufacturing, Quality, Engineering, and other cross-functional teams to resolve technical challenges

+ Execute and interpret analytical testing using techniques such as HPLC, spectroscopy, and related laboratory instrumentation

+ Ensure compliance with cGMP regulations, internal quality systems, and safety requirements

+ Author, review, and maintain technical documentation, protocols, reports, and SOPs

+ Provide technical training and support to manufacturing and laboratory personnel

+ Support aseptic processing activities and work in cleanroom environments as required

+ Provide occasional weekend or off-hours support to meet manufacturing needs.

Keys to Success

Education

Bachelor’s Degree in a related scientific field** **required

Education

Experience in product or process development, including scale-up and technology transfer processes for both immediate and controlled release dosage forms preferred.

1-3 years of experience in a manufacturing environment preferred

Experience working in cGMP-regulated environment

Project Management experience preferred

Hands-on experience with analytical techniques and laboratory instrumentation

Experience supporting process validation, technology transfer, and scale-up activities preferred

Familiarity with aseptic techniques and cleanroom operations

Experience with risk assessment tools and root cause analysis methodologies

Knowledge, Skills, and Abilities

Knowledge

Strong understanding of cGMP requirements, regulatory compliance, and quality systems

Skills

Proficiency with Microsoft Office Suite and manufacturing/quality systems

Strong technical writing, documentation, and data analysis skills

Effective project management and organizational capabilities

Abilities

Ability to work independently while contributing effectively within cross-functional teams

Strong problem-solving and troubleshooting capabilities

Excellent written and verbal communication skills

Ability to train, mentor, and support team members

Additional language skills are a plus

Physical Requirements / Work Environment

Ability to work in controlled manufacturing and cleanroom environments

Must be able to wear required personal protective equipment (PPE)

Ability to lift up to** **35 lbs

Ability to stand for extended periods

Benefits

We offer competitive remuneration, an annual incentive plan bonus, healthcare, and a wide range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization and outstanding career and development prospects. Our culture is built on** **integrity, intensity, involvement, and innovation** **.

Our Total Rewards Include:

Medical, Dental, and Vision benefits effective Day 1

Paid Time Off and designated paid holidays

Retirement Savings Plan

Tuition Reimbursement

Other

Relocation assistance:** **Not provided

Must be legally authorized to work in the United States without sponsorship now or in the future

Must be able to pass a comprehensive background check, including a drug screening

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.