Scientist I, QC (ICP-MS, ICP-OES)
As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
SCIENTIST I, QC
Job Description
The Scientist I, QC will perform a variety of analytical procedures in the analysis of cell culture media and raw materials by various testing techniques including ICP-MS and ICP-OES.
Will be expected to: Enter data, review data to ensure the final release of finished product and/or raw materials in applicable systems. Follow and adhere to GLPs, cGMPs, SOPs and all safety regulations as they apply to the laboratory and work areas.
Represent the laboratory on cross-departmental teams as needed.
What will you do in this role?
Read, understand and interpret analytical procedures
Prioritize individual workflow of daily tests and activities to ensure departmental goals are achieved
Report data and compare results to established specifications or anticipated trends
Work with Research and Development and Manufacturing Sciences to facilitate the development of and/or transfer of new assays.
Interact with diverse internal functional groups to resolve complex problems.
Write WINS and SOPs
Respond to internal and external audit observations in order to identify and implement appropriate corrective and preventive actions.
Multitask in a fast-paced environment and prioritize work as necessary
Work independently, as well as on teams within the Cell Culture, Analytical Chemistry, Microbiology, Environmental and Incoming Quality Control Laboratories.
Education/Experience:
Bachelor's Degree in Scientific/Technical field (i.e. Chemistry, Biology) or Associate's Degree with 2+ years experience with Metals testing
Experience with ICP-MS and/or ICP-OES
Experience with Qtegra Software is preferred
Understanding of principles, theory, and operation of various analytical instruments and techniques (e.g., HPLC, GC).
Experience with cGMP, GLP, CLIA or other lab regulations
Excellent interpersonal skills
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
ACCESSIBILITY/DISABILITY ACCESS
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.
This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
Compensation and Benefits
The salary range estimated for this position based in New York is $58,100.00–$64,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
