Job Market Guide: Quality Control Manager jobs in Hartford-New Haven

Competition
Avg
0.559934
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Quality Control Managers in Hartford-New Haven. Quality Control Managers in Hartford-New Haven have between ${} and ${} years of experience, averaging $${} years of experience.

79 Quality Control Manager jobs in Hartford-New Haven

Boston, MA
Achieve quality assurance operational objectives by generating metric analysis for the necessary departments for review; finding root causes and issuing internal correction if needed.
industry
Consumer Electronics
experience
5 - 7 years

Cambridge, MA
Review and approve clinical assay test methods and make recommendations for process improvements and clarity; establish and maintain robust and compliant deviation management, CAPA, and change control systems/processes.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Cambridge, MA
Manages laboratory personnel and oversees their selection, performance management, mentoring, and career development.
industry
Biotech/Pharma
experience
8 - 10 years

$70K - $90K - Hartford, CT
Searching for a Packaging Quality Control Manager.
industry
Manufacturing / Packaging
experience
Not Specified

$80K - $130K - Wellesley, MA
The Senior GCP Auditor will be a critical team member who contributes to the implementation of risk-based GCP audit programs and clinical compliance oversight.
industry
Biotech/Pharma
experience
5 - 7 years

QC Lab Manager

Cambridge, MA
Coordinate the testing of raw materials and finished goods with outside labs when required, and allocate results of said testing to the necessary persons.
industry
Biotech/Pharma
experience
5 - 7 years

$80K - $130K - Waltham, MA
The Senior GCP Auditor will be a critical team member who contributes to the implementation of risk-based GCP audit programs and clinical compliance oversight.
industry
Biotech/Pharma
experience
5 - 7 years

GCP QA Manager

$90K - $130K - Paterson, NJ
This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
industry
Biotech/Pharma
experience
5 - 7 years

GCP QA Manager

$90K - $130K - Clifton, NJ
This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
industry
Biotech/Pharma
experience
5 - 7 years

GCP QA Manager

$90K - $130K - Fair Lawn, NJ
This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
industry
Biotech/Pharma
experience
5 - 7 years

Canton, MA
Responsible for quality oversight of operations at company Biologics Canton facility, a vaccine manufacturing facility. QA Compliance main function is to ensure CGMPs are being adhered to during manufacturing operations.
industry
Life Sciences & Research
experience
5 - 7 years

$80K - $130K - Dedham, MA
The Senior GCP Auditor will be a critical team member who contributes to the implementation of risk-based GCP audit programs and clinical compliance oversight.
industry
Biotech/Pharma
experience
5 - 7 years

GCP QA Manager

$90K - $130K - Hackensack, NJ
This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
industry
Biotech/Pharma
experience
5 - 7 years

Canton, MA
Responsible for quality oversight of operations at company Biologics Canton facility, a vaccine manufacturing facility. QA Compliance main function is to ensure CGMPs are being adhered to during manufacturing operations.
industry
Life Sciences & Research
experience
5 - 7 years

GCP QA Manager

$90K - $130K - Paramus, NJ
This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
industry
Biotech/Pharma
experience
5 - 7 years

Canton, MA
Build strong and positive cross functional working relationships by working to include them in the improvement activities / training, making sure their needs and requirements are carefully considered.
industry
Life Sciences & Research
experience
5 - 7 years

$80K - $130K - Weston, MA
The Senior GCP Auditor will be a critical team member who contributes to the implementation of risk-based GCP audit programs and clinical compliance oversight.
industry
Biotech/Pharma
experience
5 - 7 years

Rensselaer, NY
Responsible for reviews of drug product process validation and device process validation plans, protocols and reports.
industry
Biotech/Pharma
experience
5 - 7 years

Rensselaer, NY
Acts as a single point of contact for consistent product quality oversight and to maintain product knowledge while helping project teams achieve their goals.
industry
Biotech/Pharma
experience
5 - 7 years

$80K - $130K - Brookline, MA
The Senior GCP Auditor will be a critical team member who contributes to the implementation of risk-based GCP audit programs and clinical compliance oversight.
industry
Biotech/Pharma
experience
5 - 7 years

Hicksville, NY
Formulates and maintains standards and objectives to enhance the functionality of the Units. Coordinate objectives with managers to ensure maximization of resources and optimization of performance of the diverse functions within the Units.
industry
Financial Services
experience
8 - 10 years

GCP QA Manager

$90K - $130K - Ridgewood, NJ
This position will provide day to day support to the GXP QA Director in clinical operations/Non-clinical and manage CROs, CMOs, investigator sites, and all relevant vendors to support clinical trials.
industry
Biotech/Pharma
experience
5 - 7 years

Ridgefield, NJ
Follows up with Change Owners and task owners to ensure that all required actions are completed in a timely and compliant manner to ensure proper closeout of the change.
industry
Life Sciences & Research
experience
5 - 7 years

QA Automation Manager

Boston, MA
Ensure high quality automation deliverables based on Selenium WebDriver for web product and Appium for mobile applications; manage test scripts development and execution, collect test data and report on test results.
industry
Business Services
experience
11 - 15 years

Manager, QA IT Quality

Rensselaer, NY
Provide ongoing support to the Quality Auditing function with respect to IT vendors and audits.
industry
Biotech/Pharma
experience
5 - 7 years