817 Qa Manager Information Technology jobs in Burlington,MA

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QA Manager

Heico

Nashua, NH 03063

~ 35 min Onsite

Bachelor of Science or equivalent RF Microwave industry work experience.
Knowledgeable in industry drawing standards and Military Specifications
Experience assessing customer specifications, statements of work; etc.
Working with purchasing staff to establish quality requirements from external suppliers;
Defining quality procedures in conjunction with operating staff;
Setting up and maintaining controls and documentation procedures;
Identifying relevant quality-related training needs and delivering training;
Collating and analyzing performance data and charts against defined parameters;
Ensuring tests and procedures are properly understood, carried out and evaluated and that product modifications are investigated if necessary;
Supervising technical staff in carrying out tests and checks;
Writing technical and management systems reports;
Liaising with customers' auditors and ensuring the execution of corrective action and compliance with customers' specifications;
Establishing standards of service for customers

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New, Posted 10 hours ago

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ResumeLibrary

Information Technology Auditor

MassMutual

Boston, MA 02112

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Research Development Quality Inspection Management Lead (GCP/GVP)

Merck Group

Billerica, MA 01821

RemoteHealth InsurancePaid Time OffRetirement Benefit

Minimum 8 years QA experience or other relevant experience with a minimum of 5 years in Clinical QA
Bachelor's degree with a focus on scientific subjects
Sound experience with Regulatory Authorities inspections by major authorities (MHRA, FDA, EMA, PMDA)
In depth knowledge of drug development processes and respective international regulations/guidelines
Broad knowledge of relevant GxP areas (GCP, GLP, GVP)
Travel globally up to 20%

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New, Posted 16 hours ago

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Quality Manager (Onsite)

Collins Aerospace

Peabody, MA 01960

~ 25 min OnsiteFlexible ScheduleEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

U.S. citizenship is required, as onlyU.S. citizens are authorized to access information under this program/contract.

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Quality Assurance (QA) Inspector

SynQor

Salem, NH 03079

~ 36 min Onsite

Working knowledge of IPC-A-610 Class 2 & Class 3 standards.
Familiarity with IPC-A-620 and J-STD-001 inspection criteria.
Basic computer skills.
Ability to read & communicate in English

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Associate Scientist I

Pace Analytical Life Sciences

Woburn, MA 01801

$28/hr

~ 10 min OnsiteUrgently HiringEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's degree in chemistry/biochemistry, or a closely related field; OR an equivalent combination of education, training, and experience.
Fundamental principles, practices, and techniques of chemistry/biochemistry.
Standard understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures.
Fundamental methods to resolve chemistry/biochemistry problems, questions, and concerns.
Standard understanding of applicable chemistry/biochemistry laws, codes, and regulations.
Understanding of standard testing tools, instruments, and calibration.
Computer applications and systems related to the work.
Principles and practices to serving as an effective project team member.
Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations.
Correct business English, including spelling, grammar, and punctuation.
Performing fundamental professional-level chemistry/biochemistry duties in a variety of assigned areas.
Overseeing and administering standard chemistry/biochemistry functions.
Training others in policies and procedures related to the work.
Serving as a team member and the development and management of projects.
Operating in a both a team and individual contributor environment.
Interpreting, applying, and explaining applicable laws, codes, and regulations.
Preparing fundamental functionals reports, correspondence, and other written materials.
Using initiative and independent judgment within established department guidelines.
Using tact, discretion, and prudence in working with those contacted in the course of the work.
Performing effective oral presentations to large and small groups across functional peers and the department.
Contributing effectively to the accomplishment of team or work unit goals, objectives and activities.
Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work.

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Information Technology Professional

US Navy

Lawrence, MA 01841

New, Posted 1 day ago

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Quality Technician

Johnson Controls

Burlington, MA 01805

OnsiteHealth InsurancePaid Time OffRetirement Benefit

High school diploma or equivalent.
1–3 years of experience in a quality inspection or technician role
Proficient in using measuring and inspection tools and reading technical drawings.
Basic understanding of statistical process control (SPC) and sampling techniques.
Strong computer skills, including Microsoft Excel and quality management software.
Must be a United States Citizen

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New, Posted 3 hours ago

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Associate Director, Global Regulatory Affairs CMC

Takeda Pharmaceutical

Boston, MA 02108

Hybrid~ 24 minUrgently HiringEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

BS/BA Degree in a Scientific Discipline, Advanced Degree (M.S., Ph.D., etc.) preferred.
10+ years of overall biopharmaceutical/device industry experience with 5+ years pharmaceutical Regulatory CMC or Device experience, including experience leading a major variation/amendment, supporting an initial IND/IMPD preparation, or supporting an initial NDA/BLA.
Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support.
Proven ability to understand and communicate regulatory strategy to drug development, registration, and post-market support teams.
Analyze issues with attention to detail.
Base regulatory strategy recommendations on precedents and other regulatory intelligence as well as regulations and guidelines.
Able to deal with issues of critical importance with minimal supervision. Exercises good judgement in elevating and communicating actual or potential issues to line management.
Understands who is responsible for different decisions and escalates as necessary.
Applies decisions taken by the company.
Demonstrates emerging leadership, problem-solving ability, flexibility and values teamwork.
Intentionally promotes an inclusive culture.
Applies the given prioritization framework with limited support.
Excellent written and oral communication skills required.
Ability to independently define CMC content (data and documentation) requirements for regulatory submissions and reviews this content for conformance with established requirement.
With minimal supervision, develops, plans, executes and manages regulatory submissions per the GRA CMC Product Team technical regulatory strategy.