Process Engineer III

Sanofi; Framingham (MA); On-site; USD 74,000 - 108,000; Full time

Job summary

A leading healthcare company seeks a Process Engineer III in Framingham, MA, responsible for supporting mammalian cell culture processes and enhancing manufacturing operations. The ideal candidate will bring a strong background in bioprocess engineering, excellent communication skills, and a Bachelor’s or Master’s degree in a relevant field, with opportunities for career progression and a comprehensive rewards package.

Benefits

Health and wellness programs

14 weeks gender-neutral parental leave

Career advancement opportunities

Supportive team environment

Qualifications

• 5 years of industry experience for Bachelor's, or 3 years for Master's.
• Experience in technology transfer and commercial manufacturing operations.
• Understanding of Good Manufacturing Practices.

Responsibilities

• Provide technical support for commercial products at CMOs.
• Review manufacturing processes and production data.
• Lead cross-functional teams and projects.

Skills

Biologics development

Bioprocess engineering

Technical writing

Communication skills

Statistical analysis

Education

Bachelor's degree in engineering or science

Master's degree in engineering or science

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

job requisition id R2808440

Job Title: Process Engineer III

Location: Framingham, MA

About the Job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.

The Recombinant Mammalian DS Platform function within global MSAT is the owner of Life Cycle Management of mammalian cell culture based DS Processes within Sanofi biologics manufacturing network. We deliver innovative, robust, and cost-effective next generation processes, enable launch of new products, and provide commercial manufacturing support. The function is responsible for tech transfer activities including process fit-gap assessment, process validation, prepare dossier sections, & PAI support to enable launch of new and LCM products.

Our expansive portfolio covers 17 products, 5 modalities, 3 expression systems within 12 internal and external global sites in US and EU. We will be supporting launch of 20 new products in next 5 years including monoclonal and multi-specific antibodies, fusion protein, antibody-drug conjugate. In recent years we have successfully established second-generation manufacturing process with continuous process platform. We are pursuing future innovations such as digital labs, factory of future and advanced analytics-based process understanding and control.

The successful candidate will work with a group of scientists and engineers responsible for support of commercial mammalian cell culture processes in the external manufacturing MSAT group. This group support commercial operations across a diverse network of manufacturing facilities and external partners. Key responsibilities may differ among employees with same job title and may change over time in accordance with business needs.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities

Provide technical support and routine process monitoring for commercial products manufactured at CMOs.

Reviews manufacturing processes, deviations, and/or development and production data.

Reviews manufacturing batch records, protocols, and control strategies.

Provide technical support and data analysis for investigations and deviation resolution.

Represent upstream team as an SME or technical lead in cross-site, cross-functional teams.

Recommends changes or additional experiments to improve quality, productivity, recovery, and overall efficiency.

Interacts with colleagues and external partners from various functions, such as Engineering, Manufacturing, and Quality departments

Oversees and reports on overall manufacturing progress.

Designs and conducts necessary experiments, interprets results.

May provide technical guidance to less experienced staff.

May lead small technical project teams and implement project plans.

May lead technology transfer efforts of small project teams between groups/organizations.

May support regulatory filings

About You

Basic Qualifications

Bachelor’s degree in engineering or science with 5 years of industry experience or master’s degree in engineering or science with 3 years of industry experience

Experience in biologics development, bioprocess engineering, technology transfer, and / or commercial manufacturing operations

Experience with Good Manufacturing Practices and supporting a commercial facility

Preferred Qualifications

Experience with Good Manufacturing Practices and supporting a commercial facility

Experience in cell culture (direct lab experience a plus)

Experience with equipment qualification and process validation

Familiarity with formal root cause analysis and/or risk assessment

Experience working with statistical analysis software and investigative data analysis

Experience with project leadership

Experience communicating with cross functional teams

Strong technical writing and communication skills

Proficient in Microsoft Word, Excel, and PowerPoint

Special Working Conditions

Ability to gown and gain entry to manufacturing areas

Ability to travel (up to 20% of time)

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SG
#LI-GZ

#LI-Onsite
#vhd

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

North America Applicants Only

The salary range for this position is:

$74,250.00 - $107,250.00

Job Title: Process Engineer III

Location: Framingham, MA

About the Job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.

The Recombinant Mammalian DS Platform function within global MSAT is the owner of Life Cycle Management of mammalian cell culture based DS Processes within Sanofi biologics manufacturing network. We deliver innovative, robust, and cost-effective next generation processes, enable launch of new products, and provide commercial manufacturing support. The function is responsible for tech transfer activities including process fit-gap assessment, process validation, prepare dossier sections, & PAI support to enable launch of new and LCM products.

Our expansive portfolio covers 17 products, 5 modalities, 3 expression systems within 12 internal and external global sites in US and EU. We will be supporting launch of 20 new products in next 5 years including monoclonal and multi-specific antibodies, fusion protein, antibody-drug conjugate. In recent years we have successfully established second-generation manufacturing process with continuous process platform. We are pursuing future innovations such as digital labs, factory of future and advanced analytics-based process understanding and control.

The successful candidate will work with a group of scientists and engineers responsible for support of commercial mammalian cell culture processes in the external manufacturing MSAT group. This group support commercial operations across a diverse network of manufacturing facilities and external partners. Key responsibilities may differ among employees with same job title and may change over time in accordance with business needs.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities

• Provide technical support and routine process monitoring for commercial products manufactured at CMOs.

• Reviews manufacturing processes, deviations, and/or development and production data.

• Reviews manufacturing batch records, protocols, and control strategies.

• Provide technical support and data analysis for investigations and deviation resolution.

• Represent upstream team as an SME or technical lead in cross-site, cross-functional teams.

• Recommends changes or additional experiments to improve quality, productivity, recovery, and overall efficiency.

• Interacts with colleagues and external partners from various functions, such as Engineering, Manufacturing, and Quality departments

• Oversees and reports on overall manufacturing progress.

• Designs and conducts necessary experiments, interprets results.

• May provide technical guidance to less experienced staff.

• May lead small technical project teams and implement project plans.

• May lead technology transfer efforts of small project teams between groups/organizations.

• May support regulatory filings

About You

Basic Qualifications

• Bachelor’s degree in engineering or science with 5 years of industry experience or master’s degree in engineering or science with 3 years of industry experience

• Experience in biologics development, bioprocess engineering, technology transfer, and / or commercial manufacturing operations

• Experience with Good Manufacturing Practices and supporting a commercial facility

Preferred Qualifications

• Experience with Good Manufacturing Practices and supporting a commercial facility

• Experience in cell culture (direct lab experience a plus)

• Experience with equipment qualification and process validation

• Familiarity with formal root cause analysis and/or risk assessment

• Experience working with statistical analysis software and investigative data analysis

• Experience with project leadership

• Experience communicating with cross functional teams

• Strong technical writing and communication skills

• Proficient in Microsoft Word, Excel, and PowerPoint

Special Working Conditions

• Ability to gown and gain entry to manufacturing areas

• Ability to travel (up to 20% of time)

Why Choose Us?

• Bring the miracles of science to life alongside a supportive, future-focused team.

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SG
#LI-GZ

#LI-Onsite
#vhd

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

North America Applicants Only

The salary range for this position is:

$74,250.00 - $107,250.00

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK .

Sanofi

Why Sanofi

As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.