Top 190 Quality manager Jobs in Hudson, Ma

Senior Manager, Quality Control GMP
Cogent Biosciences —Waltham, MA
- $155,000 - $185,000 a year
- Remote
- 5 years
- Bachelor of Science
- Bachelor's degree
- Free parking
- Paid parental leave
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Director of Quality Improvement
Saint Vincent Hospital —Worcester, MA
- $61.58 - $95.44 an hour
- Full-time
- Nursing
- Doctoral degree
- RN License
- Health savings account
- Health insurance
Quality Manager for CNC Machine Shop (Watertown, MA)
Confidential-Manufacturing —Watertown, MA
- $90,000 - $130,000 a year
- Full-time
- Management
- Engineering
- Windows
- Profit sharing
- Health insurance
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Director of Clinical Quality and Resident Care (RN license required)
Rogerson Communities —Boston, MA
- $135,000 - $150,000 a year
- Full-time
- Nursing
- 7 years
- RN License
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12d
Training, Quality and Operations Manager
Walker, Inc. —Needham, MA
- $72,000 - $90,000 a year
- Full-time
- Bilingual
- Background check
- LMFT
- Health savings account
- Health insurance
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Quality Assurance and Regulatory Affairs Manager
Taza Chocolate —Somerville, MA
- $80,000 - $95,000 a year
- Full-time
- Microsoft Excel
- 3 years
- Senior level
- Disability insurance
- Health insurance
2d
Quality Director (24568)
Ardent Staffing Solutions —Westborough, MA
- $130,000 - $145,000 a year
- Full-time
- Background check
- Engineering
- Pass drug screening
- Disability insurance
- Health insurance
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Quality Manager
Goodwin Recruiting —Watertown, MA
- $95,000 - $120,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Bachelor's degree
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Quality Control Manager
Micro Tech Staffing Group —Hudson, MA
- $85,000 - $110,000 a year
- Full-time
- 5 years
- Analysis skills
- Supervising experience
Quick Apply
1d
RA/QA Director
NeuroSync Inc. —Holliston, MA
- $160,000 - $180,000 a year
- Full-time
- Master's degree
- In-person
- Senior level
- Health insurance
- Dental insurance
Quick Apply
3d
Quality Manager
Staffworks Group —Bellingham, MA
- $35 an hour
- Full-time
- Mid-level
- Analysis skills
- Supervising experience
- Health insurance
- Dental insurance
Quick Apply
1d
GMP Compliance Manager (Devens, MA)
CSI International —Devens, MA
- $80,000 a year
- Full-time
- Background check
- Mid-level
- Analysis skills
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Research Development Quality Inspection Management Lead (GCP/GVP)
Merck Group —Billerica, MA
- $139,400 - $209,200 a year
- Full-time
- 8 years
- Bachelor's degree
- Travel
- Health insurance
- Paid time off
1d
Quality Manager - Industrial Mfg.
Search Staffing Group Inc. —Franklin, MA
- $125,000 - $140,000 a year
- Full-time
- Bachelor of Science
- Engineering
- 8 years
- Health insurance
- 401(k)
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4d
Sr Manager, Quality and Change Management
Hologic —Marlborough, MA
- $134,700 - $224,500 a year
- Engineering
- 8 years
- Senior level
Sr. QC Manager
Nova Biomedical —Waltham, MA
- $150,000 - $170,000 a year
- Full-time
- 5 years
- Product management
- Ability to sit for extended periods
- Paid holidays
- Health insurance
Quick Apply
11d
QA Manager (Manager, Quality Assurance)
Redwire Space —Marlborough, MA
- $126,000 - $165,000 a year
- Full-time
- Background check
- Schematics
- 5 years
Quick Apply
Quality Manager
AMETEK, Inc. —Chelmsford, MA
- $90,000 - $125,000 a year
- Microsoft Excel
- Management
- 5 years
- Opportunities for advancement
5d
Manager, Quality Operations
Viridian Therapeutics, Inc. —Waltham, MA
- $118,000 - $145,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- 5 years
- Paid parental leave
- AD&D insurance
Quick Apply
International Quality Assurance Manager (Quality Management Systems)
AngioDynamics —Marlborough, MA
- $121,000 - $152,000 a year
- Full-time
- Office
- 3 years
- Ability to lift 50 pounds
Quick Apply

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Senior Manager, Quality Control GMP

Cogent Biosciences -
Waltham, MA

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Job Details

$155,000 - $185,000 a year

Benefits

Free parking
Paid parental leave
Disability insurance
Health insurance
On-site gym
Dental insurance
Tuition reimbursement
Paid time off
Parental leave
Vision insurance
401(k) matching

Qualifications

Corrective and preventive actions (CAPA)
Pharmaceutical company experience
Pharmaceutical analysis
Quality control experience within pharmaceutical industry
Test validation method
Pharmaceutical manufacturing facility experience

Full Job Description

Who We Are:

Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing.

The Role:

We are seeking a Senior Manager, Quality Control GMP to provide scientific and technical leadership for Quality Control activities supporting clinical and commercial manufacturing. This role is a senior individual contributor within the Quality organization and is responsible for driving method lifecycle management, ensuring GMP compliance, and supporting release and stability testing strategies for drug substance and drug product.

The successful candidate will serve as a key QC subject‑matter expert, working closely with CMC, Analytical Development, Manufacturing, Quality Assurance, and external partners to ensure robust, compliant, and efficient QC operations. This role requires strong leadership in complex problem solving, as well as the ability to influence cross‑functional teams and external vendors.

Responsibilities:

Provide scientific leadership for QC GMP activities, including method transfer, qualification, validation, and lifecycle management for drug substance (DS) and drug product (DP).
Serve as a QC subject‑matter expert supporting release and stability testing, including data review, trending, and interpretation.
Lead or support investigations of deviations, OOS, and OOT results, including root cause analysis and development of corrective and preventive actions (CAPAs).
Collaborate closely with Analytical Development and CMC teams to ensure successful method transfers to QC laboratories and external CMOs.
Provide oversight of QC activities conducted at contract testing laboratories and manufacturing partners, including review of data packages and ensuring compliance with quality and regulatory requirements.
Contribute to the development and execution of control strategies for small‑molecule drug substance and drug product.
Author, review, and approve QC‑related documents, including methods, specifications, protocols, validation reports, and regulatory submission content.
Support regulatory inspections and audits, including preparation, response, and follow‑up activities.
Identify opportunities for continuous improvement in QC processes, technologies, and compliance practices.
Mentor junior staff and serve as a technical resource across functional teams.

Qualifications:

Ph.D. in Chemistry, Pharmaceutical Sciences, or a related discipline, with significant experience in QC or analytical sciences in a GMP environment; or M.S./B.S. with substantial relevant industry experience.
5-8 years of experience with QC testing and GMP compliance supporting clinical and/or commercial stage programs.
Strong expertise in analytical techniques relevant to small‑molecule pharmaceuticals (e.g., HPLC/UPLC, GC, dissolution, spectroscopic methods, and wet chemistry).
Deep understanding of method validation, transfer, and lifecycle management in a regulated environment.
Demonstrated experience supporting or leading deviation investigations (OOS/OOT) and CAPA processes.
Working knowledge of global regulatory requirements, including FDA, EMA, ICH guidelines, and compendial standards (USP, EP).
Experience working with and overseeing external laboratories, CMOs, or CROs.
Proven ability to operate independently, manage multiple priorities, and influence cross‑functional stakeholders.
Strong written and verbal communication skills, with the ability to clearly present technical concepts and data.

Salary Range:

$155,000 - 185,000 USD

Target Bonus: 15%

Exact compensation will vary based on skills, experience, and location.

Our Locations

Waltham, MA: Our headquarters is located in the Greater Boston life sciences community, with an open, collaborative office environment designed to support teamwork and connection. Employees benefit from convenient on-site amenities, including free on-site parking and gym facilities in the building.

Boulder, CO: Our Boulder location is home to Cogent's discovery research organization and a key scientific hub with strong leadership based on site. Situated in the greater Denver-Boulder biopharmaceutical corridor, this office plays a central role in advancing our discovery efforts and pipeline.

Our Offer To You

At Cogent Biosciences, we offer a competitive salary, bonus, and ongoing stock awards, alongside a benefits package that sets us apart. We cover 100% of medical, dental, and vision premiums for you and your family, and help reduce out-of-pocket costs by funding up to 75% of in-network deductibles. Our benefits also include a 401(k) match with immediate vesting, generous paid time off, 12 weeks of fully paid parental leave, paid family and medical leave for all employees regardless of location, and company-paid short-term disability coverage for up to 20 weeks. Additional perks like wellness programs, tuition reimbursement, and inclusive family-forming support help you thrive at work and beyond.

We are proud to be an Equal Opportunity Employer. Our goal is to have a diverse workforce. We do not discriminate on the basis of race, age, color, religion, national origin, gender, sexual orientation, gender identity or expression, veteran status or disability, or any other status protected under federal, state, or local law. All employment is decided on the basis of qualifications, merit, and business need.

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Refine Your Search

quality manager jobs in hudson, ma

Senior Manager, Quality Control GMP

Director of Quality Improvement

Quality Manager for CNC Machine Shop (Watertown, MA)

Director of Clinical Quality and Resident Care (RN license required)

Training, Quality and Operations Manager

Quality Assurance and Regulatory Affairs Manager

Quality Director (24568)

Quality Manager

Quality Control Manager

RA/QA Director

Quality Manager

GMP Compliance Manager (Devens, MA)

Research Development Quality Inspection Management Lead (GCP/GVP)

Quality Manager - Industrial Mfg.

Sr Manager, Quality and Change Management

Sr. QC Manager

QA Manager (Manager, Quality Assurance)

Quality Manager

Manager, Quality Operations

International Quality Assurance Manager (Quality Management Systems)

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