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MSAT Site Lead - Athens

Job in Athens, Clarke County, Georgia, 30612, USA
Listing for: J&J Family of Companies
Full Time position
Listed on 2026-07-20
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn

more at  () .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

** Job Function:*
* Supply Chain Engineering

** Job Sub*
* ** Function:*
* Process Engineering

** Job Category:*
* People Leader

** All Job Posting Locations:*
* Athens, Georgia, United States of America

*
* Job Description:

*
* ** About Innovative Medicine*
* Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at  

We are searching for the best talent for a Manufacturing Science and Technology (MSAT) Site Lead! This onsite position will be located in Athens, Georgia (USA).

Join a team committed to delivering trusted therapies to the patients who need them most. In this role, you'll work alongside dedicated colleagues who care deeply about doing what's right and continuously improving the way we operate. Ready to make an impact? Apply today!

The MSAT Site Lead is responsible for providing technical leadership for small molecule drug substance (SM DS) and medical device component businesses for our Athens, GA site. They will coordinate the performance and day-to-day management of our MSAT team for the Business Unit (BU) and lead technical resources and critical processes related to new product launches, product lifecycle support, transfers, and MSAT performance tracking within our SM BU.

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* KEY RESPONSIBILITIES:

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* + Lead a team of engineers owning portfolio products in and across the BU, lifecycle management (LCM) and cleaning validation support, and monitoring and optimizing the performance of portfolio products for SM DS.

+ Represent MSAT Athens in site leadership and global SM DS leadership team meetings.

+ Works closely with Quality Assurance, R&D Partners, Maintenance and Engineering (GET), and Operations to drive value within the BU.

+ Provide technical support in partnership with Quality on any regulatory audits and inspections and serve as the Spokesperson in internal and external audits for the MSAT processes.

+ Lead and/or support complex process nonconformance events.

+ Engage with key functions within the with the global communities of practice and resources teams for process and cleaning validation, innovation, and data analytics to maintain high program compliance and implement new technologies and improvements.

+ Partner proactively within the global Synthetics Platform to drive alignment, share knowledge, and deliver value from optimizing collaborations.

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* QUALIFICATIONS:

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* *
* EDUCATION:

*
* + Minimum of a University/Bachelor's or equivalent degree is required;
Master's degree and/or a focused degree in Chemical Engineering or related field is preferred

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* EXPERIENCE AND SKILLS:

*
* *
* Required:

*
* + Minimum of 8 years of relevant work experience

+ Demonstrated experience within a Pharmaceutical manufacturing environment

+ Strong understanding and knowledge of Quality & Compliance / regulatory requirements (GMP/EHS)

+ Strong expertise in chemical manufacturing processes, technologies, and products, as well as strong business acumen with synthetics drug substance

+ Demonstrated experience managing, organizing, planning, and coordinating projects

+ Demonstrated ability to effectively influence…
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