Qa Jobs in New Bedford, MA
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Qa • new bedford ma
Last updated: 5 days ago
The QA QMS Associate is responsible for ensuring compliance with both internal and external quality standards, playing a pivotal role in maintaining and enhancing the Quality Management System (QMS...Show moreLast updated: 6 days ago
Analytical Quality Assurance Supervisor.Confirming and ensuring the compliance of the protocols and reports of method validations / verifications / comparison reports and any other study reports.Monito...Show moreLast updated: 5 days ago
Under the guidance of the VP of Quality, Compliance and Risk, the Home Health Coder-QA Specialist provides guidance to other members of the clinical team on overall quality and completeness of clin...Show moreLast updated: 30+ days ago
Tonix is a biopharmaceutical company, publicly traded on NASDAQ (ticker : TNXP).The Company is focused on commercializing, developing, discovering and licensing therapeutics to treat and prevent hum...Show moreLast updated: 25 days ago
- Promoted
QA QMS Associate
ActalentNew Bedford, MA, USFull-time
- Promoted
Analytical QA Supervisor
Nesco ResourceNew Bedford, MA, USFull-time
Home Health Coder / QA Specialist
Tufts MedicineRemote, MassachusettsRemote
Part-time
- Promoted
Senior Director, QA Systems
Tonix Pharmaceuticals IncNew Bedford, MA, USFull-time
The average salary range is between $ 63,806 and $ 132,432 year , with the average salary hovering around $ 94,769 year .
- chief medical officer (from $ 134,966 to $ 250,000 year)
- psychiatrist (from $ 157,610 to $ 247,200 year)
- engineering director (from $ 140,000 to $ 225,000 year)
- vp engineering (from $ 156,925 to $ 225,000 year)
- vp of engineering (from $ 180,000 to $ 225,000 year)
- dentist (from $ 76,016 to $ 214,500 year)
- real estate developer (from $ 84,375 to $ 195,000 year)
- clinical director (from $ 90,000 to $ 193,604 year)
- forensic pathologist (from $ 104,309 to $ 192,773 year)
- front end engineer (from $ 120,000 to $ 191,154 year)
- Bridgeport, CT (from $ 82,524 to $ 168,219 year)
- Santa Ana, CA (from $ 74,278 to $ 159,732 year)
- Santa Rosa, CA (from $ 75,166 to $ 159,508 year)
- Santa Clara, CA (from $ 75,860 to $ 159,471 year)
- Fremont, CA (from $ 63,375 to $ 159,400 year)
- San Bernardino, CA (from $ 59,423 to $ 154,536 year)
- Seattle, WA (from $ 62,500 to $ 154,010 year)
- San Mateo, CA (from $ 59,421 to $ 153,946 year)
- San Jose, CA (from $ 59,668 to $ 152,424 year)
- San Diego, CA (from $ 60,109 to $ 152,330 year)
The average salary range is between $ 42,898 and $ 117,763 year , with the average salary hovering around $ 77,798 year .
QA QMS Associate
ActalentNew Bedford, MA, US6 days ago
Job type
- Full-time
Job description
QA QMS Associate
The QA QMS Associate is responsible for ensuring compliance with both internal and external quality standards, playing a pivotal role in maintaining and enhancing the Quality Management System (QMS) in accordance with Good Manufacturing Practice (GMP) and regulatory requirements.
Responsibilities
Assist in the development, implementation, and maintenance of the QMS in line with GMP and regulatory requirements.
Maintain and ensure proper documentation of all quality systems and records.
Oversee document control processes, ensuring SOPs, work instructions, and other quality documents are up to date and correctly implemented.
Assist in the collection, analysis, and reporting of quality data, including quality metrics, CAPA reports, and audit findings.
Support investigations of deviations, non-conformances, and customer complaints, ensuring appropriate follow-up and resolution.
Provide training and guidance to employees on QMS-related processes and regulatory requirements.
Ensure compliance with all regulatory requirements.
Support risk assessments and help mitigate potential quality risks to product safety and compliance.
Familiarity with pharmaceutical operations, preferably MDI, to ensure required compliance.
Familiarity with TrackWise applications for handling Deviation and CAPA.
Prepare and review investigations related to deviation, OOS, market complaints, and microbiological failure.
Prepare and review trends related to various QMS elements like Deviations, CAPA, Change Request, and Environmental monitoring.
Preparation and review of the Annual Product Quality Review.
Fulfill the requirements of regulatory submission while closely working with regulatory teams.
Prepare and review risk assessments (FMECA) for various facilities, equipment, processes, and particular events.
Prepare and review elemental impurities risk assessment and nitrosamine-related risk assessment.
Prepare audit reports, document findings, and provide actionable recommendations for improvement.
Essential Skills
Quality auditing
Quality assurance
Quality management system
Batch record review
Deviation investigations
Out of Specifications (OOS)
Out of Trends (OOT)
CAPA
Change control
Additional Skills & Qualifications
Advanced vocational training or education in pharmaceutical manufacturing, industrial management, or related field from an accredited institution.
Bachelor's degree in a scientific discipline such as biology, chemistry, pharmacy, or related field is preferred.
Minimum of 3 years of experience in MDI or combination products is preferred.
Proficient in Microsoft Office tools, SAP, and other business applications.
Ability to influence decision-making and facilitate completion of work towards achieving business goals.
Effective interpersonal relationship skills and ability to work in a team environment.
Proficiency in English, including usage, spelling, grammar, and punctuation.
Current Good Manufacturing Practices (cGMP) knowledge.
Self-starter demonstrating initiative with seeking additional training or direction.
Strong organization and leadership skills, both written and verbal.
Detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.
Work Environment
You will be working with a small team of 15 people in the quality department, with significant cross-collaboration with different departments. This role operates on a first shift from 8 : 00 am to 5 : 00 pm, Monday to Friday.
Company is offering up to 6K for relocation
Pay and Benefits
The pay range for this position is $74000.00 - $95000.00 / yr.
Will Sponsor OPT-H1B, Relocation Assistance up to $6,000, 10% annual bonuses based on fiscal year, Health, Vision, Dental, 401K
Workplace Type
This is a fully onsite position in Fall River, MA.
Application Deadline
This position is anticipated to close on Aug 18, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actALENTaccommodation@actalentservices.com for other accommodation options.