JobMonkey, Inc.
Life Technologies (Thermo Fisher Scientific). Ohio, Cincinnati
JobMonkey, Inc., Cincinnati, Ohio, United States, 45208
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.
Education
Bachelor's Degree in a related scientific field required
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
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
#J-18808-Ljbffr
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.
Education
Bachelor's Degree in a related scientific field required
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
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
#J-18808-Ljbffr