13,500 Data Review jobs in the United States

Data Review Pharmacist
2nd Shift Available | Not Patient Facing | Offers Benefits | Long-Term Opportunity
Job Description
We are seeking a dedicated and detail-oriented Data Review Pharmacist to join our Customer Service Center. This role is essential in ensuring the accuracy and efficiency of our medication dispensing processes.
Responsibilities
+ Review prescription data for accuracy and compliance with regulatory standards.
+ Conduct clinical assessments and verify medication appropriateness before fulfillment.
+ Enter and audit patient demographics, insurance details, and prescription information in pharmacy systems.
+ Collaborate with physicians and patients to resolve exceptions and ensure quality assurance.
+ Support specialized programs requiring tailored data handling.
+ Maintain HIPAA compliance and contribute to continuous process improvement.
Essential Skills
+ Doctor of Pharmacy (Pharm.D.) degree from an accredited institution.
+ Active pharmacist license in the state of Minnesota.
+ Minimum of 1 year of experience in a pharmacy setting, with a focus on data review and medication dispensing.
+ Strong analytical skills, attention to detail, and proficiency in pharmacy management software.
+ Excellent verbal and written communication skills.
+ In-depth knowledge of pharmacotherapy, prescription processing, and regulatory requirements.
Additional Skills & Qualifications
+ Experience with fulfillment, supervision, MTM, inventory control, Medicare, and retail pharmacy.
Work Environment
Work in a closed door Customer Service Center in a combination of production and office settings. Varying schedules are available. This newly opened facility offers numerous opportunities for advancement and leadership
Pay and Benefits
The pay range for this position is $65.00 - $74.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Brooklyn Park,MN.
Application Deadline
This position is anticipated to close on Sep 1, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Data Review Pharmacist
2nd Shift Available | Not Patient Facing | Offers Benefits | Long-Term Opportunity
Job Description
We are seeking a dedicated and detail-oriented Data Review Pharmacist to join our Customer Service Center. This role is essential in ensuring the accuracy and efficiency of our medication dispensing processes.
Responsibilities
+ Review prescription data for accuracy and compliance with regulatory standards.
+ Conduct clinical assessments and verify medication appropriateness before fulfillment.
+ Enter and audit patient demographics, insurance details, and prescription information in pharmacy systems.
+ Collaborate with physicians and patients to resolve exceptions and ensure quality assurance.
+ Support specialized programs requiring tailored data handling.
+ Maintain HIPAA compliance and contribute to continuous process improvement.
Essential Skills
+ Doctor of Pharmacy (Pharm.D.) degree from an accredited institution.
+ Active pharmacist license in the state of Minnesota.
+ Minimum of 1 year of experience in a pharmacy setting, with a focus on data review and medication dispensing.
+ Strong analytical skills, attention to detail, and proficiency in pharmacy management software.
+ Excellent verbal and written communication skills.
+ In-depth knowledge of pharmacotherapy, prescription processing, and regulatory requirements.
Additional Skills & Qualifications
+ Experience with fulfillment, supervision, MTM, inventory control, Medicare, and retail pharmacy.
Work Environment
Work in a closed door Customer Service Center in a combination of production and office settings. Varying schedules are available. This newly opened facility offers numerous opportunities for advancement and leadership
Pay and Benefits
The pay range for this position is $65.00 - $74.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Brooklyn Park,MN.
Application Deadline
This position is anticipated to close on Sep 1, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.
BASIC SUMMARY:
Responsible for reviewing all study data to ensure it is complete and GLP compliant. Ensure that all data received for review follows SOP guidelines that apply to the recording of study data. Interact with Quality Assurance staff as needed.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
+ Complete data review on all paper and electronic data produced in Operational departments.
+ Ensure all forms that require data review and electronic data are in compliance with Standard Operating Procedures (SOPs) and forms are updated as needed.
+ Ensure all data corrections are completed by the appropriate staff members and that they are completed correctly.
+ Communicate with department management and supervisors regarding any issues related to data collection that impact the recording of data.
+ Assist in departmental training by providing assistance with training on correct methods of data notation and correction as it relates to study data review.
+ Assist in revising and developing department forms.
+ Archive, collate, and organize all completed and reviewed data and/or file as appropriate.
+ Interact with Quality Assurance regarding data that is received for review. Collaborate with QA staff to ensure GLPs are being followed for the recording of data.
+ Assist with department filing as needed.
+ Complete intermittent checks on study activities to ensure that documentation of data being collected is in compliance with SOPs and GLPs.
+ Perform all other related duties as assigned.
QUALIFICATIONS:
+ Education: High school diploma or General Education Degree (G.E.D.).
+ Experience: Minimum of 1 year related experience. Experience in an animal research facility preferred. GLP experience preferred.
_An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above._
+ Certification/Licensure: None
+ Other: Strong organizational skills and acute attention to detail. Basic understanding of processes used for study data collection. Basic understanding of SOPs, GLPs and other applicable regulatory guidelines governing the recording and review of study data.
The pay for this position is $18.50/hr.
**About Safety Assessment**
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
**Equal Employment Opportunity**
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit

At Charles River, we are passionate about improving the quality of people's lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
**Job Summary**
We are seeking a **Data Review Assistant** for our **Safety Assessment** site located **in** **Reno, Nevada.**
The following are responsibilities related to this role.
Provides administrative, logistical and technical support for Scientific staff conducting studies or supporting functions for operations of the laboratory. Coordinates all laboratory support, pre-study activities, method development, method validation, study activities, data and/or reporting activities. Responsible for data review for completeness, quality or QC against the applicable protocol or procedure. May be responsible for drafting client correspondence, study correspondence, reporting or direct client interaction. Interacts with other departments, scientific staff, and sponsors either locally or across sites.
**Job Qualifications**
The following are minimum qualifications related to this position:
**Education:** High school diploma or General Education Degree (G.E.D.).
**Experience:** Minimum of 1 year related experience. Experience in an animal research facility preferred. GLP experience preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
**Other:** Strong organizational skills and acute attention to detail. Basic understanding of processes used for study data collection. Basic understanding of SOPs, GLPs and other applicable regulatory guidelines governing the recording and review of study data.
Compensation Data
The starting pay for this opportunity is $19.50/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
**About Safety Assessment**
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
**Equal Employment Opportunity**
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit

Data Quality Review Clerk

The Research Foundation for Mental Hygiene and the New York State Office of Mental Health is seeking two Data Quality Review Clerks to join the Office of Population Health and Evaluation Medical Informatics Unit. This unit is responsible for collecting, entering, verifying, analyzing, and reporting data from various survey projects related to mental health services and programs. The ideal candidate will have excellent communication skills, both verbal and written, confidence and professionalism in obtaining information over the phone, strong organizational and attention to detail skills, and the ability to work independently and collaboratively on multiple tasks and deadlines.

Duties and Responsibilities include:

• Contact hospital staff via telephone to confirm and validate daily hospital survey information
• Update hospital data validation tracking documents, help desk guides, and data dictionary as needed
• Prepare and mail survey packages to mental health programs across the state
• Provide customer support to survey respondents and staff via phone, email, and the Help Center application
• Review the data collected from surveys for quality, accuracy, and completeness
• Assist in maintaining and improving the systems for data cleansing and data entry
• Enter the data into various computer applications using web, keyboard or scanning methods
• Track the receipt of completed surveys and follow up with providers and field offices as needed
• Review and process applications for exemptions from survey reporting requirements
• Conduct testing of computer applications used for data collection and reporting
• Extract and analyze data from applications and generate statistical reports
• Complete all assigned tasks in a timely and efficient manner with minimal errors
• Handle sensitive and confidential data in compliance with HIPAA (Health Insurance Portability and Accountability Act) procedures
• Other tasks may be assigned as necessary.

Minimum Qualifications:

• A minimum of a 2 year degree, preferably a 4 year degree, in a relevant field

Preferred Qualifications:

• Demonstrable accurate and fast data entry skills
• 1 year experience with data collection, testing computer applications, MS Office products (Excel, Access), or similar software

Work Location: 150 Broadway, Menands, NY 12204

To Apply: Submit an application through our website at . Please note only applications submitted through our website will be considered.

The Mission of the Research Foundation for Mental Hygiene, Inc. (RFMH) is to promote the mental health of all New Yorkers, with a focus on providing hope and supporting recovery for adults with serious mental illness and children with serious emotional disturbances. Applicants with lived mental health experience are encouraged to apply. RFMH is deeply committed to supporting underserved individuals, organizations, and communities. To this end, RFMH is focused on implementing activities and initiatives to reduce disparities in access, quality, and treatment outcomes for underserved populations. A critical component of these efforts is ensuring that RFMH is a diverse and inclusive workplace where all employees' unique attributes and skills are valued and utilized to support the mission of the Agency. RFMH is an equal opportunity/affirmative action employer.

The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Employer/Minority/Women/Disabled/Veteran Employer. VEVRAA 41 CFR 60-300.5(a) compliant.

Forensic Scientist Data Review II

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

Working at Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with high employer contribution.
• Tuition reimbursement, the student debt program and education benefit - an affordable and convenient path to getting a bachelor's degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity Abbott Rapid Diagnostics (formerly Alere) is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies. The position of DOT GC-LC/MS Operator/Transcriptionist is within Toxicology located at Gretna, LA at Alere Toxicology Services. In this role, the individual will be responsible for operating a Gas Chromatograph/Mass Spectrometer and LC-MS/MS for confirmatory testing in accordance with the SAMHSA mandatory guidelines and those of other regulatory organizations for all non-negative test results. This job also requires the individual to perform QC duties.

Shift: Monday, Tuesday, Friday & Saturday 9:00 pm to 7:30 am

What You'll Work On:

• Process regulated samples that fall under SAMHSA/DOT regulations and are subject to interviews during NLCP inspection and/or audits.
• Operation of the GC/MS and/or LC-MS/MS instruments.
• Perform initial review of data.
• Preparation and extraction of samples for GC/MS and LC-MS/MS confirmation as needed.
• Operate lab equipment necessary to perform extraction as needed.
• Prepare validation samples for new controls, calibrators and reagents.
• Documentation of QC validation results.
• Storage of supplies and disposal of empty boxes as needed.
• Adhere to all security procedures for ensuring confidentiality of donor information.
• Must comply with company policies.

Required Qualifications:

• BS degree in science or equivalent related field.

Preferred Qualifications:

• Advanced ability to understand analytical techniques and procedures.
• Advanced ability to understand laboratory instrumentation.
• Ability to understand certification requirements for SAMHSA, CAP-FUDT, and other regulatory bodies.
• Advanced ability to understand the function of a Laboratory Information System (LIS) and other laboratory computer systems.

Work Environment:

• Climate-controlled office and testing laboratory environment.
• May be potential exposure to toxic or hazardous materials.

The base pay for this position is $20.60 $41.20 per hour. In specific locations, the pay range may vary from the range posted. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**_Forensic Scientist Data Review II_**
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
+ An excellent retirement savings plan with high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
Abbott Rapid Diagnostics (formerly Alere) is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies. The position of DOT GC-LC/MS Operator/Transcriptionist is within Toxicology located at Gretna, LA at Alere Toxicology Services. In this role, the individual will be responsible for operating a Gas Chromatograph/Mass Spectrometer and LC-MS/MS for confirmatory testing in accordance with the SAMHSA mandatory guidelines and those of other regulatory organizations for all non-negative test results. This job also requires the individual to perform QC duties.
**Shift:**
Monday, Tuesday, Friday & Saturday
9:00 pm to 7:30 am
**What You'll Work On**
+ Process regulated samples that fall under SAMHSA/DOT regulations and are subject to interviews during NLCP inspection and/or audits
+ Operation of the GC/MS and/or LC-MS/MS instruments
+ Perform initial review of data
+ Preparation and extraction of samples for GC/MS and LC-MS/MS confirmation as needed
+ Operate lab equipment necessary to perform extraction as needed
+ Prepare validation samples for new controls, calibrators and reagents
+ Documentation of QC validation results
+ Storage of supplies and disposal of empty boxes as needed
+ Adhere to all security procedures for ensuring confidentiality of donor information
+ Must comply with company policies
**Required Qualifications**
+ BS degree in science or equivalent related field
**Preferred Qualifications**
+ Advanced ability to understand analytical techniques and procedures
+ Advanced ability to understand laboratory instrumentation
+ Ability to understand certification requirements for SAMHSA, CAP-FUDT, and other regulatory bodies
+ Advanced ability to understand the function of a Laboratory Information System (LIS) and other laboratory computer systems
**Work Environment**
+ Climate-controlled office and testing laboratory environment
+ May be potential exposure to toxic or hazardous materials
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews.
The base pay for this position is $20.60 - $41.20 per hour. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**Work Schedule**
First Shift (Days)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner.
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.
**Key responsibilities:**
+ Perform technical and quality reviews of internal and external documents, including raw data, stability protocols/reports, CoAs/stability data reports, risk assessments, sampling plans, shelf-life reports and etc.
+ Enter and trend stability data in SLIM system and generate stability timepoint summary reports.
+ Establish/extend DS and DP shelf lives and generate shelf-life reports based on stability data.
+ Plan, manage and communicate stability pulls and ensure stability testing occurs within specified testing windows.
**Education and Experience:**
+ Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar
+ **Sr. Scientist:** Previous experience that provides the knowledge, skills, and abilities to perform the job **(comparable to 4+ years')**
+ OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job **(comparable to 2+ years')**
+ OR **PhD**
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Knowledge, Skills and Abilities:**
+ Proven Experience with stability studies, stability protocols/reports, CoAs/stability data reports, risk assessments, sampling plans, shelf-life reports, including raw data and external documents.
+ Stability data in SLIM system and generate stability timepoint summary reports.
+ DS and DP shelf lives and generate shelf-life reports based on stability data.
+ Plan, manage and communicate stability pulls and ensure stability testing occurs within specified testing windows.
+ Attention to detail and ability to multitask, review tons of data.
**Working Environment:**
Below is listed the working environment/requirements for this role:
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
Able to work upright and stationary and/or standing for typical working hours.
Able to lift and move objects up to 25 pounds
Able to work in non-traditional work environments.
Able to use and learn standard office equipment and technology with
proficiency.
May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
**Benefits**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
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.

Job Description

• Eurofins is seeking a self-motivated, adaptable, and positive individual who can work both independently and as part of a team in a client-facing environment
• The primary purpose of this position is to perform analysis of manufacturing data from chromatography and other purification processes.
  • Investigations will be performed to identify root cause and path forward for any out of trend data.
  • Presentations will then be created to provide recommendations for actions when necessary
• Troubleshooting equipment and processes, maintaining clean orderly work spaces, and ensuring compliance are all responsibilities of this role.
• Completes laboratory documentation and reviews logbook data.
• Complies with all pertinent regulatory agency requirements and maintains inspection readiness
• Occasional opportunities for preparation and operation of chromatographic systems for small scale lab experiments.
  • After completion of the experiments, data and statistical analysis will be completed to understand relationships and impacts to processes

Qualifications:
Qualifications

• Bachelor's degree in life sciences is required.
  • Chemistry background is preferred.
• cGMP experience and experience with technical writing is desirable.
• Authorization to work in the United States indefinitely without restriction or sponsorship.
• Must have good general computer skills and be proficient in Microsoft Office
• Excellent communication (oral and written) and attention to detail
• Applicants must be able to thrive working in a fast-paced environment
• Applicants should be able to multitask while remaining within appropriate timeframes and maintaining accuracy
• Applicants must prioritize statistical analysis work, reporting, and documentation.
• Candidates living within a commutable distance of Rensselaer, NY are encouraged to apply.

Additional Information

• Position is full-time, the role is 1st Shift Monday-Friday 8am-4:30pm _ ***_. The compensation range is between $19.50-22.50/hr.

** What we offer: **

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Yearly goal-based bonus & eligibility for merit-based
• #LI-EB1

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.