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
- 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 9 Corporate Holidays Per Year
- Excellent Healthcare Dental and Vision Benefits
- Healthcare and Dependent Flexible Spending Accounts
- Long/Short Term Disability Coverage
- 401(k) with a Company Match
- Parental Leave
- Tuition Reimbursement Program
- Additional Add-On Benefits/Discounts
Pay range for this opportunity is$105400.00 - $130000.00. This position is incentive plan eligible with a target of 15% depending on performance.
Minimum pay rates offered will comply with county/city minimums if higher than range listed. Pay rates are based on a number of factors including but not limited to local labor market costs years of relevant experience education professional certifications foreign language fluency etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits:STERIS Benefits
Open until position is filled.
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
.If you need assistance completing the application process please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited hired trained transferred and promoted in all job groups regardless of race color religion age disability national origin citizenship status military or veteran status sex (including pregnancy childbirth and related medical conditions) sexual orientation gender identity genetic information and any other category protected by federal state or local law. We are not only committed to this policy by our status as a federal government contractor but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program absent the data metrics required by 60-741.44(k) shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your locations HR Office during normal business hours.