Top 426 Data review specialist, quality control Jobs in Northborough, Ma

Data Review Specialist, Quality Control
Ocular Therapeutix —Bedford, MA
- $98,000 - $113,000 a year
- Mid-level
- Bachelor's degree
- Commercial
14d
Quality Control Data Reviewer
Rentschler Biopharma SE —Milford, MA
- $90,000 - $110,000 a year
- Microsoft Outlook
- Bachelor of Science
- Mid-level
- Health insurance
- 401(k)
9d
Mechanical Inspector for CNC Machine Shop (Watertown, MA)
Confidential-Manufacturing —Watertown, MA
- $60,000 - $80,000 a year
- Full-time
- Mid-level
- In-person
- 1 year
- Profit sharing
- Health insurance
Quick Apply
Medical Billing Specialist - FULL TIME - Framingham -At least 2 yr exp required
Complete Pain Care —Framingham, MA
- $24 - $32 an hour
- Online Application
- Spanish
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
5h
(IQC) Inspector II - **4-Day Work Week**
Kopin Corporation —Westborough, MA
- $23 - $27 an hour
- Email
- Computer literacy
- Basic math
- ERP systems
- Health insurance
- Dental insurance
Quick Apply
1d
Quality Technician (1st shift)
BlackTree Technical Group —Acton, MA
- $32 an hour
- Full-time
- Background check
- Computer literacy
- Basic math
Quick Apply
Quality Control Specialist II - CMM Operator
CoorsTek Inc —Worcester, MA
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Basic math
Quick Apply
Process Inspector (Union Job)
Wyman Gordon —North Grafton, MA
- $24.19 - $32.03 an hour
- Full-time
- Background check
- In-person
- Entry level
- Health savings account
- Health insurance
Quick Apply
6d
Mechanical & Electrical Quality Inspector (Second Shift)
Masis Professional Group —Westborough, MA
- $23.00 - $25.75 an hour
- Day shift
- Mid-level
- 3 years
- Communication skills
- Opportunities for advancement
Quick Apply
14d
Final Quality Inspector I (23480)
Ardent Staffing Solutions —Westborough, MA
- Background check
- Pass drug screening
- High school diploma or GED
- AD&D insurance
- Paid holidays
Quick Apply
Quality Inspector - Advanced Electro Mechanical
Masis Staffing Solutions —West Boylston, MA
- Mid-level
- Office
- 3 years
Quick Apply
Professional Land Surveyor
Masis Professional Group —Lunenburg, MA
- $85,000 - $110,000 a year
- Full-time
- Construction site
- Research
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Quality Inspector Technician
Myomo, Inc —Burlington, MA
- $26 - $28 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Neurology
Quick Apply
14d
Quality Manager
Consigli Construction —Milford, MA
- $139,000 - $159,000 a year
- Full-time
- Construction site
- Engineering
- Mid-level
Quick Apply
Quality Control Inspector
Connexion Systems and Engineering, Inc. —Shrewsbury, MA
- $30 - $37 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
- Health insurance
- Dental insurance
Quick Apply
8d
Mechanical Quality Inspector
Prince Industries LLC —Pepperell, MA
- $23 - $27 an hour
- 8 hour shift
- Ability to walk for extended periods
- English
- Mid-level
- Health savings account
- AD&D insurance
Quick Apply
Sheetmetal Quality Inspector
ACP Waterjet Inc. —Littleton, MA
- $24 - $30 an hour
- Full-time
- Background check
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply
Revenue Cycle Specialist
Human Services Management Corporation —Milford, MA
- $23 - $26 an hour
- Full-time
- Hybrid work
- HIPAA
- Mid-level
- Office
Quick Apply
3rd shift Quality Inspector
Temp-Secure Staffing —Leominster, MA
- $19 - $20 an hour
- Overnight shift
- English
- In-person
- Manufacturing
Quick Apply
Production Assembler / Quality Inspector - Devens, MA or Clinton, MA
Adecco —Devens, MA
- $16.34 - $21.00 an hour
- Contract
- Military encouraged
- Organizational skills
- Fair chance
- Commuter assistance
- Paid holidays
Quick Apply
14d

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Data Review Specialist, Quality Control

Ocular Therapeutix -
Bedford, MA

Apply Now

Job Details

$98,000 - $113,000 a year
14 days ago

Qualifications

GMP
Data integrity and documentation
Bachelor's degree
Pharmaceutical analysis
Quality control experience within pharmaceutical industry
Microbiological analysis
Technical Proficiency

Full Job Description

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.

Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity.

Position Summary:

The Data Review Specialist will apply strong technical knowledge of laboratory operations, analytical data review, data integrity requirements, and quality systems to perform thorough reviews of analytical chemistry, microbiology, stability, and release testing data for accuracy, completeness, scientific soundness, and compliance with cGMP, GLP, and ALCOA+ expectations. This position is critical for supporting batch release, stability studies, environmental monitoring, method validation, and device testing.

In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging patterns, atypical results, potential OOT signals, and opportunities for improved product understanding. The Data Review Specialist will serve as a trusted partner to QC, QA, Stability, Manufacturing, Supply Chain, and Analytical Development stakeholders.

Key Responsibilities:

Quality Control Data Review

Review analytical raw data (HPLC/UPLC, GC, spectrophotometry, pH, dissolution, device function & performance testing) to ensure accuracy in calculations, instrument suitability, standards, sequences, and chromatographic integration.
Review microbiology data (bioburden, endotoxin, sterility, ID, EM, growth promotion, device-specific assays)
Review and support trending of stability data across applicable drug products, raw materials, and device-related attributes to identify emerging trends, atypical results, potential OOT signals, and data patterns requiring escalation.
Assist with interpretation of stability data in support of timepoint completion, stability reports, annual product reviews, regulatory submissions, and product lifecycle monitoring.
Support monitoring of released testing data for commercial and clinical batches, including review of assay, impurities/degradation products, dissolution/drug release, microbiological, and device performance data where applicable.
Collaborate with QC Stability, Raw Materials, QA, Manufacturing, Supply Chain, and Analytical Development to evaluate data trends and determine whether observed patterns require investigation, CAPA, procedural updates, or enhanced monitoring.
Support trending and monitoring of raw material data, including supplier lot-to-lot variability, retest/expiry data, CoA verification trends, and recurring analytical or documentation issues.

Documentation & Compliance

Ensure reviewed data packages meet cGMP, GLP, FDA/EMA, internal SOP, ALCOA+, and data integrity expectations for lot release, stability, raw materials, device testing, method validation, and regulatory support. Conduct timely and thorough review of data packages to support lot release, stability pulls, device testing, and method verification/validation activities.
Identify and document discrepancies, atypical results, potential data integrity concerns, and review comments; work with QC, QA, and originating groups to resolve issues in a timely manner.
Support OOS, OOT, deviations, CAPAs, audits, APR/PQR inputs, and regulatory requests by evaluating analytical, microbiological, stability, release, and raw material data for trends, anomalies, or potential root causes.

Quality Systems & Continuous Improvement

Recommend and support improvements to data review workflows, documentation templates, JPM, LIMS/Empower interfaces, Smartsheet trackers, and data integrity practices.
Generate and maintain reports, trackers, dashboards, and KPIs to support QC management review, workload visibility, product quality monitoring, and continuous improvement initiatives.
Serve as a technical resource to QC analysts by reinforcing best practices in documentation, audit trail review, ALCOA+ expectations, data monitoring, and inspection readiness

Cross-Functional Collaboration

Work cross-functionally with QC Chemistry, Raw Materials, Analytical Development, QC Microbiology, QA, Manufacturing, Supply Chain, and Product Development groups.
Communicate delays, data discrepancies, and potential risks to QC and QA leadership promptly.
Support cross-functional data requests related to product release, investigations, validations, or regulatory submissions.

Qualifications:

Bachelor's degree in Chemistry, Microbiology, Biochemistry, Biology, or related scientific discipline.
5+ years in a QC laboratory, or data review role or a similar GMP-regulated environment, with a track record of strong performance, reliability, and increasing responsibility.
Strong working knowledge of cGMP, GLP, and data integrity expectations (ALCOA+).
Ability to independently review laboratory data, identify discrepancies, and collaborate effectively with peers and stakeholders to resolve issues in a timely manner.
Experience reviewing analytical chemistry and microbiology data (bioburden, endotoxin, EM trending, sterility).
Familiarity with chromatography software (e.g., Empower) and microbiology testing documentation.
Proficiency with electronic data management systems, including JPM, LIMS, Smartsheets and Empower.
Familiarity with statistical software, JMP preferred.
Prior experience with method validation and stability study protocols is a plus.

#LI-LM1

Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at https://www.ocutx.com/privacy-policy/. For the Privacy Notice for California Job Applicants, please see CCPA Applicant Notice.

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Refine Your Search

data review specialist, quality control jobs in northborough, ma

Data Review Specialist, Quality Control

Quality Control Data Reviewer

Mechanical Inspector for CNC Machine Shop (Watertown, MA)

Medical Billing Specialist - FULL TIME - Framingham -At least 2 yr exp required

(IQC) Inspector II - 4-Day Work Week

Quality Technician (1st shift)

Quality Control Specialist II - CMM Operator

Process Inspector (Union Job)

Mechanical & Electrical Quality Inspector (Second Shift)

Final Quality Inspector I (23480)

Quality Inspector - Advanced Electro Mechanical

Professional Land Surveyor

Quality Inspector Technician

Quality Manager

Quality Control Inspector

Mechanical Quality Inspector

Sheetmetal Quality Inspector

Revenue Cycle Specialist

3rd shift Quality Inspector

Production Assembler / Quality Inspector - Devens, MA or Clinton, MA

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