Data Reviewer - GMP Biopharm
JOB DESCRIPTION
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
This is a fully remote role supporting our GMP Laboratory in Middleton, WI. We welcome applications from all locations within the US.
Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.
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.
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
Discover Impactful Work:
The Data Reviewer performs review of a variety of routine and complex analytical analysis experiments that are conducted on pharmaceutical and biopharmaceutical compounds with various formulations and/or biological matrices. Ensures analyses are following validated or experimental analytical procedures, and compare results to methodology, protocol and product specifications, Standard Operating Procedures (SOPs) acceptance criteria, and Good Manufacturing Practices (GMP). Reviews data entered into databases and reports and monitors the quality of the laboratory data. Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis review independently.
A day in the Life:
- Evaluates laboratory data for compliance with analytical methods, client directives, and SOPs.
- Reviews sample results for scientific soundness, completeness, accurate representation of the data, and final reported results.
- Communicates with laboratory staff to proactively maintain the quality of laboratory documentation.
- Delivers review findings noting deficiencies within the analytical data or reports in a clear and concise manner.
- Escalate significant deficiencies to the project leader or supervisor for assessment.
- Facilitates in conversations with lab staff on best documentation practices and addressing quality findings.
- Advocates for quality and review process changes.
- Identifies and supports process improvement initiatives.
- Performs other duties as assigned.
Keys to Success:
Education
- Bachelor’s degree or equivalent and relevant formal academic / vocational qualification
Experience
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’) or equivalent combination of education, training, and experience.
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, Abilities
- Previous experience with formal data review in GMP Lab strongly preferred
- Thorough knowledge of SOPs and Federal Regulations to include GLP and GMP
- Thorough knowledge of chromatography may be required
- To demonstrate behaviors which align to the 4i Values of Thermo Fisher Scientific
- Strong technical knowledge including an understanding of laboratory procedures, methodology, and standards
- Strong verbal and written communication skills
- Strong attention to detail
- Ability to balance time and remain focused on work to meet goals
- Ability to train staff on basic review techniques
- Ability to independently review laboratory reports and analytical methods
- Ability to deal with multiple and changing priorities
- Ability to provide clear and concise feedback and/or documentation of results
- Ability to work in a collaborative team environment
- Ability to work efficiently in a remote capacity
Work Environment
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. 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.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today!
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 View phone number on us.fitly.work*. 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.
- The Data Reviewer is responsible for ensuring the completion, quality, and compliance of laboratory data and reports produced within the Quality... ...Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) standards. This position will manage deadlines for review...DataContract work
- ...ensures adherence to record retention policies, batch record review, and more effectively data retrieval. This position also ensures that Certificates of... ...quality system. Follow Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Review...Data
- ...to bring new therapies to patients in need. The Position The Data Reviewer independently performs technical review of laboratory data and... ...to ensure compliance with analytical methods, specifications, GMP/GDP requirements, and data integrity standards. This role exercises...Data
- ...Qualifications MasterControl experience Experience supporting Quality, GMP, or regulated environments Document control or records retention... ...and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law....DataLocal area
- ...de nodige metadata aan om de transitie naar een nieuw systeem mogelijk te maken Je organiseert meetings met de juiste personen om de data aan te vullen Je volgt de projectstatus op aan de business kant en werkt hierbij samen met de projectmanager binnen de IT-dienst Je...Data
- ...control.Provide leadership on strategic initiatives and advise stakeholders on best practices.Ensure high-quality use of various Common Data Environments (CDE).Supervise document control teams on large, complex programs involving multiple business groups.Organize and...DataFor contractorsWork at officeFlexible hours
$35 - $43 per hour
...Data Reviewer As a Data Reviewer, you will be responsible for reviewing data from validations and technology transfers of QC test methods for products and materials to ensure data integrity. You will collaborate with QC chemists to address any data or reporting issues...DataTemporary work$25 - $33.35 per hour
...the design, construction, and operation of SHINE's Chrysalis medical isotope production facility. The position provides document and data support for the on-site Engineering, Construction, Procurement, and Operations teams, ensuring the adequacy of approved documents...DataHourly payWork at officeRemote work- ...product documentation. In this role, you will be responsible for reviewing and managing documents stored in both paper archives and... ...Retrieval: Classify, log, index, and store hard-copy and electronic data using consistent naming conventions. - Ensure digital copies are...DataContract workFor contractorsWork at office
- ...related administrative tasks. Key Requirements Bachelor’s Degree Data entry experience Ability to use databases, scanners, and other... ...record archiving procedures Functions Basic use of computer Reviewing and sorting of file documents on file archives Data entry of...DataMonday to Friday
- ...inboxes, creating work requests to provide work for other teams, reviewing documents, and effectively communicating with customers and co-... ...acuity to perform an activity such as: preparing and analyzing data, reviewing emails; transcribing; viewing a computer terminal....DataFull time
- ...and be able to schedule overlapping activities to meet deadlines. Review and analyze title information and documents, LTC, and title... ...received, upload them into the document management system and enter data into appropriate database system(s) with close attention to how...DataWork at office
- ...ensure proper resources are used at each business process workflow step. Watch for leading indicators of project risks from workflow data and communicate to project team, as well as work to resolve the issue. • Provide training to company and partner users as...DataLong term contractFor contractorsWork at officeRemote work
- ...orders, and specifications to verify completeness and accuracy of data. Confers with document originators or engineering liaison... ...assign out monthly Quality Audits and log appropriately for each review. Minimum Knowledge, Skills and Abilities Required: High school diploma...DataWork at officeRelocation
$23 per hour
...generated content, evaluating factual accuracy, or comparing responses — when projects are available. Responsibilities Carefully review provided data (text, images, or videos) Review tasks submitted by the Annotators team and ensure quality assurance/quality control. Label...DataPart timeFreelanceRemote work$25 - $33.35 per hour
...medical isotope production facility (the Chrysalis). The Document Control/Record Management Specialist position provides document and data support for the on-site Engineering, Construction, Procurement, and Operations teams, ensuring the adequacy of approved documents...DataHourly payWork at officeRemote work$28.5k - $33.28k
...Technologies is seeking a detail-oriented Document Processing & Data Entry Clerk to join our team onsite in Janesville, Wisconsin. In... ...hiring between August and September 2026. Applications will be reviewed on an ongoing basis during this timeframe, and selected candidates...DataFull timePart timeWork at officeMonday to FridayFlexible hours- ...documentation packages in accordance with project and certification requirements. Job Duties Prepare and submit final documentation packages (Data Books/Quality Data Packages/IOMs) which include spec sheets, MTRs, inspection reports, change notices, AS BUILT drawing packages,...DataWork at officeWorldwide
- ...managers to ensure the project is not adversely impacted, and ensure the delivery of projects to compliant standards Analyse and review a range of data to identify key themes and trends and use the outputs to produce recommendations that support project decision-making Use...DataWork at officeImmediate startFlexible hours
- Eightelevengroup is seeking an LKC Document Administrator in Pleasant Prairie, Wisconsin. This role involves reconciling controlled forms and organizing quality documentation in compliance with QA procedures. The ideal candidate will have strong attention to detail and ...
$27 - $35 per hour
...of way procedure for the project. Ensures that all right of way data is being input into the database correctly. Responsible for the... ...preparation of all acquisition packages prior to issuing to Land Agents. Reviews all executed documents for accuracy. Reviews payments for...DataFull timeTemporary workPart timeWork at officeLocal area- ...Responsibilities include setting up and maintaining documents in AGILE, managing part numbers in ORACLE, and maintaining BOMs; you will transfer data from legacy systems and manage ECOs while ensuring proper routing and #J-18808-Ljbffr SANMINA-SCI TECHNOLOGY INDIA PRIVATE LIMITEDData
- ...accurate, and compliant prior to distribution Label Production & Data Validation Generate shipping labels using internal data... ...new or junior associates Participate in audits and compliance reviews Qualifications High level of accuracy and strong attention...DataContract workWork at officeImmediate start
$20 per hour
...you will support insurance operations by receiving, processing, reviewing, classifying, indexing, and distributing documents and mail.... ...responsibilities under tight deadlines. ~ Basic computer and data entry skills. ~ Comfortable navigating multiple systems and applications...DataWeekly payFull timeMonday to FridayShift workDay shift- ...POSITION SUMMARY Provides a variety of loan support duties, primarily reviewing loan files for compliance with Bank policies, procedures, and... ...missing documentation with lending team. Verifies accuracy of data used for the completion of loan documentation. Notes exceptions...DataFull timeLocal area
- ...products and services provided Obtains physician orders for products and services provide Complying with insurance benefits & completes data entry requirements Maintains all patient status information on an ongoing basis Maintains database of physician ordersCollaborates...DataFull timeTemporary workLocal areaMonday to Friday
- ...food safety, regulatory, operational, and training documents are reviewed, approved, distributed, revised, archived, and retained in... ...work environment. Food Safety and Good Manufacturing Practices (GMP) Follow all Food Safety and Good Manufacturing Practices (GMP) standards...Contract workWork experience placement
- ...all project documentation throughout the entire project lifecycle - from engineering to commissioning. Thanks to your experience in GMP environments and industrial projects, you will ensure that documentation is processed completely, traceably, and compliantly. What Will...For contractors
- ...table, so we can truly know and help our clients, communities, and each other. CLA is seeking to hire an experienced Seasonal Tax Reviewer to join our talented tax team. The position offers flexibility and a collaborative work environment. This role is responsible...Casual workSeasonal work
- ...Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job... ...performance management, coaching and mentoring. Reviews and approves requests for paid time off,... ..., deviations, and QA facility and data audits. Prepares and implements SOPs and...DataFull timeWork at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Data Reviewer - GMP Biopharm. Be the first to apply!



