At STERIS we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Do you want to spend your working time making a difference in the world around you Are you motivated by impactful work If so then a career with STERIS in our Life Sciences team could be a great fit for you.
This is an excellent opportunity for candidates wanting to join a team of internationally known experts presenting at global industry conferences administering virtual and hands on professional education programs publishing articles and assisting pharmaceutical and biopharmaceutical industry Customers in resolving their complex issues. As a Technical Services Manager you will be a subject matter expert for contamination control and validation within the pharmaceutical and biopharmaceutical industry. The position requires providing technical information and onsite support for global Customers and managing projects related to contamination control product technology application and validation working closely with other departments including R&D Engineering Marketing and Sales. You will have opportunity to author and publish articles in A3P PDA ISPE and other associations peer reviewed journals present at major pharmaceutical/biopharmaceutical conferences workshops and training events and participate in industry associations and committees.
In this role you will travel both domestically and internationally about 40-50% of time.
What you will do as a Technical Services Manager
- Provide technical information and expertise to key Customer accounts for contamination control products including cleaning chemistries disinfectants sterilants and their applications integrating multiple areas of specialization (e.g. chemistry microbiology engineering validation etc.) with the objective of resolving complex pharmaceutical and biopharmaceutical industry Customer needs. Support provided through telephone and written correspondence generation of literature lab analyses and on-site evaluations.
- Manage projects and coordinates and oversees technical and/or lab activities within area of specialization. Serve as liaison with R&D groups for scientific and technical support.
- Administer global pharmaceutical and biopharmaceutical industry Customer and professional education programs. Present at industry conferences publishes articles and book chapters and participates in industry associations and task groups.
- Manage the tasks of one or more assigned team members providing direction and performance feedback.
- Contribute ideas and information for new products processes and applications relative to the business unit.
The Experience Skills and Abilities Needed
Required:
- Bachelors Degree in Science Engineering or Biological Science.
- Ten or more years experience in bench (Chemistry or Microbiology) lab supervision cleaning or disinfectant validation process engineering and/or technical support.
- If applicant holds a Masters degree five years experience required.
- Industry recognition and current knowledge of relevant pharmaceutical and biopharmaceutical industry subject matter and regulatory requirements.
- Strong project management skills including excellent verbal & written communication skills as well as presentation skills.
- Focused Customer and service orientation with ability to effectively utilize resources for technical information as needed.
- Must be able eligible to obtain a passport and have a valid drivers license.
Preferred:
- Masters Degree in Science Engineering or Biological Science.
- Experience in upstream/downstream biopharmaceutical manufacturing aseptic processing and validation.
What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health well-being and financial future.
Here is just a brief overview of what we offer:
- Base Salary Corporate Bonus Program
- Robust Training Program
- Time Off Corporate Holidays
- Laptop/Cell Phone/Company Vehicle provided
- Parental Leave
- Additional Add-On Benefits/Discounts
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information visit .
STERIS strives to be an Equal Opportunity Employer.
Required Experience:
Manager
At STERIS we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. Do you want to spend your working time making a difference in the world around you Are you motivated by impactful work If so then a c...
At STERIS we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Do you want to spend your working time making a difference in the world around you Are you motivated by impactful work If so then a career with STERIS in our Life Sciences team could be a great fit for you.
This is an excellent opportunity for candidates wanting to join a team of internationally known experts presenting at global industry conferences administering virtual and hands on professional education programs publishing articles and assisting pharmaceutical and biopharmaceutical industry Customers in resolving their complex issues. As a Technical Services Manager you will be a subject matter expert for contamination control and validation within the pharmaceutical and biopharmaceutical industry. The position requires providing technical information and onsite support for global Customers and managing projects related to contamination control product technology application and validation working closely with other departments including R&D Engineering Marketing and Sales. You will have opportunity to author and publish articles in A3P PDA ISPE and other associations peer reviewed journals present at major pharmaceutical/biopharmaceutical conferences workshops and training events and participate in industry associations and committees.
In this role you will travel both domestically and internationally about 40-50% of time.
What you will do as a Technical Services Manager
- Provide technical information and expertise to key Customer accounts for contamination control products including cleaning chemistries disinfectants sterilants and their applications integrating multiple areas of specialization (e.g. chemistry microbiology engineering validation etc.) with the objective of resolving complex pharmaceutical and biopharmaceutical industry Customer needs. Support provided through telephone and written correspondence generation of literature lab analyses and on-site evaluations.
- Manage projects and coordinates and oversees technical and/or lab activities within area of specialization. Serve as liaison with R&D groups for scientific and technical support.
- Administer global pharmaceutical and biopharmaceutical industry Customer and professional education programs. Present at industry conferences publishes articles and book chapters and participates in industry associations and task groups.
- Manage the tasks of one or more assigned team members providing direction and performance feedback.
- Contribute ideas and information for new products processes and applications relative to the business unit.
The Experience Skills and Abilities Needed
Required:
- Bachelors Degree in Science Engineering or Biological Science.
- Ten or more years experience in bench (Chemistry or Microbiology) lab supervision cleaning or disinfectant validation process engineering and/or technical support.
- If applicant holds a Masters degree five years experience required.
- Industry recognition and current knowledge of relevant pharmaceutical and biopharmaceutical industry subject matter and regulatory requirements.
- Strong project management skills including excellent verbal & written communication skills as well as presentation skills.
- Focused Customer and service orientation with ability to effectively utilize resources for technical information as needed.
- Must be able eligible to obtain a passport and have a valid drivers license.
Preferred:
- Masters Degree in Science Engineering or Biological Science.
- Experience in upstream/downstream biopharmaceutical manufacturing aseptic processing and validation.
What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health well-being and financial future.
Here is just a brief overview of what we offer:
- Base Salary Corporate Bonus Program
- Robust Training Program
- Time Off Corporate Holidays
- Laptop/Cell Phone/Company Vehicle provided
- Parental Leave
- Additional Add-On Benefits/Discounts
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information visit .
STERIS strives to be an Equal Opportunity Employer.
Required Experience:
Manager
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Posted on:
10-11-2025
Vacancies:
1 Vacancy
