Work Schedule Rotational shift nights/weekends
Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc… allowed, Cold Room/Freezers -22degreesF/-6degrees C, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Our colleagues bring our Mission to life every day, enabling customers to make the world healthier, cleaner, and safer. We support our teams with the resources needed to achieve individual career goals while advancing solutions to some of the world’s toughest challenges—from protecting the environment to ensuring food safety and developing life‑saving therapies.
Position Summary As a Team Leader in Formulation Manufacturing, you will lead a team responsible for the preparation of media and buffers, equipment preparation, and cleaning activities in a cGMP environment. You will ensure operational readiness, compliance, and efficient execution of manufacturing processes while driving continuous improvement and supporting new product introductions.
This role combines technical expertise with people leadership to deliver high‑quality pharmaceutical and biotechnology products.
Key Responsibilities
Ensure
operational readiness
for media and buffer preparation, equipment preparation, and cleaning activities
Lead and support the
day-to-day execution
of manufacturing operations in compliance with cGMP requirements
Manage, coach, and develop a team of operators to ensure high performance and engagement
Own and maintain
Work Instructions and SOPs , ensuring they are up to date and followed
Support
Technology Transfer
of new products and contribute to CVQ, PQ, and Process Validation activities
Participate in
New Product Introduction (NPI)
activities
Collaborate with cross-functional teams (Quality, Engineering, PCS, Maintenance) to resolve issues and improve processes
Drive
Manufacturing Excellence
initiatives to ensure robust and efficient operations
Support the definition and optimization of
process parameters
during routine manufacturing campaigns
Ensure compliance with
safety, quality, and regulatory requirements
Lead or support
investigations, deviations, and change controls
as required
Qualifications & Requirements
Bachelor’s degree (or higher) in Chemistry, Biochemistry, Biology, Engineering, or a related field
Minimum 2 years of experience in pharmaceutical/biotechnology manufacturing in a cGMP environment
Strong knowledge of
cGMP and regulatory requirements
Proven ability to
lead, coach, and develop teams
Strong
technical troubleshooting
and problem‑solving skills
Experience with
process validation, technology transfer, and manufacturing systems
Knowledge of
Lean principles and continuous improvement methodologies
is a plus
Excellent
communication and organizational skills
Experience with
documentation, deviations, and change control systems
Ability to work in a
cleanroom environment
and follow aseptic practices
Flexibility to work shifts, including weekends if required
What We Offer
A dynamic and innovative work environment
Opportunities for career development and growth
The chance to contribute to life‑saving therapies and global health improvements
#J-18808-Ljbffr
Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc… allowed, Cold Room/Freezers -22degreesF/-6degrees C, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Our colleagues bring our Mission to life every day, enabling customers to make the world healthier, cleaner, and safer. We support our teams with the resources needed to achieve individual career goals while advancing solutions to some of the world’s toughest challenges—from protecting the environment to ensuring food safety and developing life‑saving therapies.
Position Summary As a Team Leader in Formulation Manufacturing, you will lead a team responsible for the preparation of media and buffers, equipment preparation, and cleaning activities in a cGMP environment. You will ensure operational readiness, compliance, and efficient execution of manufacturing processes while driving continuous improvement and supporting new product introductions.
This role combines technical expertise with people leadership to deliver high‑quality pharmaceutical and biotechnology products.
Key Responsibilities
Ensure
operational readiness
for media and buffer preparation, equipment preparation, and cleaning activities
Lead and support the
day-to-day execution
of manufacturing operations in compliance with cGMP requirements
Manage, coach, and develop a team of operators to ensure high performance and engagement
Own and maintain
Work Instructions and SOPs , ensuring they are up to date and followed
Support
Technology Transfer
of new products and contribute to CVQ, PQ, and Process Validation activities
Participate in
New Product Introduction (NPI)
activities
Collaborate with cross-functional teams (Quality, Engineering, PCS, Maintenance) to resolve issues and improve processes
Drive
Manufacturing Excellence
initiatives to ensure robust and efficient operations
Support the definition and optimization of
process parameters
during routine manufacturing campaigns
Ensure compliance with
safety, quality, and regulatory requirements
Lead or support
investigations, deviations, and change controls
as required
Qualifications & Requirements
Bachelor’s degree (or higher) in Chemistry, Biochemistry, Biology, Engineering, or a related field
Minimum 2 years of experience in pharmaceutical/biotechnology manufacturing in a cGMP environment
Strong knowledge of
cGMP and regulatory requirements
Proven ability to
lead, coach, and develop teams
Strong
technical troubleshooting
and problem‑solving skills
Experience with
process validation, technology transfer, and manufacturing systems
Knowledge of
Lean principles and continuous improvement methodologies
is a plus
Excellent
communication and organizational skills
Experience with
documentation, deviations, and change control systems
Ability to work in a
cleanroom environment
and follow aseptic practices
Flexibility to work shifts, including weekends if required
What We Offer
A dynamic and innovative work environment
Opportunities for career development and growth
The chance to contribute to life‑saving therapies and global health improvements
#J-18808-Ljbffr
