What are the responsibilities and job description for the Technical Services Representative, 3rd shift position at Baxter?
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission.
The Technical Services Representative is a member of the core team and interacts directly with Manufacturing. Technical Services Representative will provide 3rd shift coverage and support for all Technical Services / Manufacturing related activities. This position will act as the representative for all Manufacturing Technical Services, Technical Transfer, and Process Validation activities that occurs, such as batch execution support and performance of Technical Service Studies. This position will also support facility related activities related to process improvements and batch release (such as filter troubleshooting and NCRs) to ensure facility metrics and client needs are met.
Essential Duties and Responsibilities (these are primary responsibilities of the role, but the incumbent will perform other duties as assigned):
Primary focus on routine Manufacturing support.
Responsible for making and delivering accurate and timely decisions pertaining to active projects on 3rd shift
Partners with Quality Assurance and impacted departmental management as necessary for proper escalation of real-time incidents and corrective action implementation.
NCR - Non-conformance report writing, CAPA ownership, and CCM action item ownership.
Filter Trouble Shooting and testing- proficiency and training on appropriate filter testing SOPs. Position will act as a subject matter expert (SME) regarding filter testing trouble-shooting issues to support batch release.
Demonstration (non-GMP) batch record creation and execution oversight / support
SOP revisions and ownership as needed
MBR and process training
FVOQ execution support
Kaizen / VIP performance and support
Ability to write, implement, review and summarize Technical Services Studies
Ability to provide technical support and expertise in the aseptic processing requirements for individual projects
Capable of evaluating product impact and responsible for advising if product meets release criteria per batch record and process validation requirements.
Job Requirements (Education, Experience and Qualifications):
Bachelor's degree required, preferably in a science or engineering related field
2 years of similar experience preferred.
Requires general knowledge of sterile parenteral manufacturing operations including (but not limited to): formulation/mixing activities, aseptic filling, equipment preparation, capping and lyophilization.
Familiar with standard operating procedures, quality/regulatory requirements pertinent to the industry.
Strong communication skills, both written and verbal, with the ability to interact with many functions and levels across the organization, including external clients when needed.
Strong organizational skills (attention to detail) and collaboration skills with the ability to meet tight deadlines and lead multiple projects concurrently.
Ability to qualify for Grade A/B areas. Aseptic gowning will be necessary on occasion. Grade C/D gowning will also be required..
Computer proficiency in Microsoft Word, Excel, Outlook and the ability to use facility software programs, such as (but not limited to) JDE and Trackwise.
Physical / Safety Requirements:
Duties may require overtime work, including off-shifts and weekends
Use of hands and fingers to manipulate office equipment and tools to assemble testing equipment is required
Position may require sitting or standing for long periods of time.
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all our employees, and we strive to be more transparent with our pay practices. To that end, this position has a salary range of $52,800 to $132,000 and also includes an annual incentive bonus, commission target, and/or equity target (strike any, if not applicable). The above range represents the expected salary range for this position. The actual salary may vary based upon several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location.
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The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
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Salary : $52,800 - $132,000