Relevant background in GXP/QC-compliant pharmaceutical laboratory environment. - Excellent verbal and written communication and interpersonal skills, problem-solving, and organizational skills ...
Relevant background in GXP/QC-compliant pharmaceutical laboratory environment. - Excellent verbal and written communication and interpersonal skills, problem-solving, and organizational skills ...
Relevant background in GXP/QC-compliant pharmaceutical laboratory environment. * Excellent verbal and written communication and interpersonal skills, problem-solving, and organizational skills.
Relevant background in GXP/QC-compliant pharmaceutical laboratory environment. * Excellent verbal and written communication and interpersonal skills, problem-solving, and organizational skills.
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Data Reviewer III
Rensselaer, NY · On-site
... pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we ... Review data generated from various analytical instrumentation including but not limited to Gas ...
Job Overview The Data Review Scientist will be responsible for reviewing laboratory data and ... Bachelor's degree in chemistry with three years' experience in a pharmaceutical and cGMP ...
Job Overview The Data Review Scientist will be responsible for reviewing laboratory data and ... Bachelor's degree in chemistry with three years' experience in a pharmaceutical and cGMP ...
Senior Data Reviewer, Quality Control
Madison, WI · On-site
$100K - $110K/yr
Bachelor's degree in chemistry or any STEM degree + 8+ years, or master's degree + 5+ years in a cGMP laboratory (pharmaceutical CMO/CRO) * Strong experience with analytical methods + data review ...
Senior Data Reviewer, Quality Control
Madison, WI · On-site
$100K - $110K/yr
Bachelor's degree in chemistry or any STEM degree + 8+ years, or master's degree + 5+ years in a cGMP laboratory (pharmaceutical CMO/CRO) * Strong experience with analytical methods + data review ...
Data Reviewer, Analytical Development
Madison, WI · On-site
$80K - $90K/yr
... pharmaceutical CMO/CRO). * Experience with analytical data review and documentation practices * Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR ...
Quick apply
Data Reviewer, Analytical Development
Madison, WI · On-site
$80K - $90K/yr
... pharmaceutical CMO/CRO). * Experience with analytical data review and documentation practices * Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR ...
Data Reviewer, Analytical Development
Verona, WI · On-site
$80K - $90K/yr
... pharmaceutical CMO/CRO). * Experience with analytical data review and documentation practices * Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR ...
Data Reviewer, Analytical Development
Verona, WI · On-site
$80K - $90K/yr
... pharmaceutical CMO/CRO). * Experience with analytical data review and documentation practices * Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR ...
Educational scientific background such as MD, PharmD, PhD, Nursing degree, MSc * ≥ 5 years of pharmaceutical clinical/medical data review experience is required, including clinical crosscheck ...
Educational scientific background such as MD, PharmD, PhD, Nursing degree, MSc * ≥ 5 years of pharmaceutical clinical/medical data review experience is required, including clinical crosscheck ...
Data Reviewer, Analytical Development
Verona, WI · On-site
$80K - $90K/yr
... pharmaceutical CMO/CRO). * Experience with analytical data review and documentation practices * Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR ...
Data Reviewer, Analytical Development
Verona, WI · On-site
$80K - $90K/yr
... pharmaceutical CMO/CRO). * Experience with analytical data review and documentation practices * Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR ...
... pharmaceutical CMO/CRO) * Strong experience with analytical methods + data review + audit trail review * Deep knowledge of GMP, data integrity, and regulatory expectations * Working knowledge of ...
... pharmaceutical CMO/CRO) * Strong experience with analytical methods + data review + audit trail review * Deep knowledge of GMP, data integrity, and regulatory expectations * Working knowledge of ...
Data Review Chemist I - Analytical Quality Assurance
Oklahoma City, OK · On-site
$23 - $26/hr
Data Review Chemist I - Analytical Quality Assurance Position Summary... Join a company where you ... Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug ...
Data Review Chemist I - Analytical Quality Assurance
Oklahoma City, OK · On-site
$23 - $26/hr
Data Review Chemist I - Analytical Quality Assurance Position Summary... Join a company where you ... Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug ...
Data Review Chemist I - Analytical Quality Assurance
Oklahoma City, OK · On-site
$23 - $26/hr
Data Review Chemist I - Analytical Quality Assurance Position Summary... Join a company where you ... Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug ...
Data Review Chemist I - Analytical Quality Assurance
Oklahoma City, OK · On-site
$23 - $26/hr
Data Review Chemist I - Analytical Quality Assurance Position Summary... Join a company where you ... Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug ...
... pharmaceutical CMO/CRO) * Experience with analytical data review and documentation practices * Working knowledge of analytical methods (HPLC, GC, LC-MS, NMR, FTIR, Appearance, pH, KF, UV spectrometry ...
... pharmaceutical CMO/CRO) * Experience with analytical data review and documentation practices * Working knowledge of analytical methods (HPLC, GC, LC-MS, NMR, FTIR, Appearance, pH, KF, UV spectrometry ...
Job Overview The Data Review Scientist will be responsible for reviewing laboratory data and ... pharmaceutical and cGMP environment highly preferred. * Experience in a laboratory environment ...
Job Overview The Data Review Scientist will be responsible for reviewing laboratory data and ... pharmaceutical and cGMP environment highly preferred. * Experience in a laboratory environment ...
The Data Review Scientist will be responsible for reviewing laboratory data and supporting ... pharmaceutical and cGMP environment highly preferred. - Experience in a laboratory environment ...
The Data Review Scientist will be responsible for reviewing laboratory data and supporting ... pharmaceutical and cGMP environment highly preferred. - Experience in a laboratory environment ...
The Data Review Scientist will be responsible for reviewing laboratory data and supporting ... pharmaceutical and cGMP environment highly preferred. - Experience in a laboratory environment ...
The Data Review Scientist will be responsible for reviewing laboratory data and supporting ... pharmaceutical and cGMP environment highly preferred. - Experience in a laboratory environment ...
Data Review Pharmacist information
See salary details
$27.88 - $32.10
2% of jobs
$32.10 - $36.32
0% of jobs
$36.32 - $40.54
0% of jobs
$40.54 - $44.76
0% of jobs
$44.76 - $48.97
5% of jobs
$48.97 - $53.19
9% of jobs
$55.91 is the 25th percentile. Wages below this are outliers.
$53.19 - $57.41
13% of jobs
The median wage is $61.32 / hr.
$57.41 - $61.63
22% of jobs
$61.63 - $65.84
21% of jobs
$66.40 is the 75th percentile. Wages above this are outliers.
$65.84 - $70.06
18% of jobs
$70.06 - $74.28
9% of jobs
$27
$60
$74
How much do data review pharmacist jobs pay per hour?
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For Data Review Pharmacist jobs, the most frequently searched job titles are:

Quality Assurance Data Review Scientist
High Point, NC • On-site
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
This job post has expired today. Applications are no longer accepted.
Cambrex rating
8.1
Based on 6 frontline employees who took The Breakroom Quiz
Job description
Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With over 40 years of experience and a growing team of over 2,200 experts servicing global clients from North America and European sites, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.
At Cambrex, our people set us apart. We're committed to attracting, nurturing, and retaining a passionate and talented team of valued experts in our fast-paced and growing company. We offer an exceptional benefits package including medical, dental, vision, Life, LTD, generous vacation in your first year, sick time, and retirement savings!
Known for our scientific and manufacturing excellence, as well as our strong customer focus, we offer a range of career opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world.
Overview:Come join our QA team of experts. The Data Review Scientist conducts data review activities for data generated by GMP Analytical for validation of analytical test methods, testing of cleaning samples, raw materials, process intermediates, final APIs, and final dosage forms, characterizing/qualifying Reference Standards, and Stability results. These data reviews are accomplished by review and approval of GMP Analytical Laboratory data located in notebooks, Material Release Forms, stability reports, methods qualifications/validations and reports, etc., as well as other documents as assigned.
Responsibilities:- Reviews chromatographic/other data and related notebooks as specified by Standard Operating Procedures (SOPs). Evaluates data to ensure compliance with analytical methods, client criteria, SOPs, and Good Manufacturing Practices (GMP).
- Must be able to understand analytical data (chromatographic and other) and scrutinize routine and non-routine testing results to ensure compliance, accuracy, and completeness of work based on documented data.
- Must be able to critically and in detailed fashion review/verify Reports, SOPs, Specifications, Analytical procedures, etc. Example: Reviews sample results tables and analytical reports for completeness and accurate representation of the data and report findings.
- Must be able to solve practical problems and deal with a variety of concrete variables in situations where limited standardization exists.
- Must be able to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
- Organizes workflow and tasks to maximize efficiency (e.g., prioritize review/writing based on client/business needs, etc.).
- Demonstrated ability to work with others at all levels of the organization and have basic knowledge of computers and industry-related software.
- Ability to work effectively under pressure to meet deadlines.
- Ensures compliance with company policies and SOPs as well as FDA and other applicable guidelines.
Fundamental understanding (experience is not required) with the following analytical technologies:
- Titrations (manual and automated)
- Basic wet chemistry
- FTIR
- NMR
- XRPD
- DSC
- HPLC
- GC
- MS
- Working knowledge of other analytical equipment common to the pharmaceutical industry.
About Cambrex
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
East Rutherford, NJ, US
Year founded
1981