Top 38 Production lead Jobs in Salisbury, Ma

Quality Manufacturing Lead
SOFIE —Haverhill, MA
- $90,000 a year
- Analysis skills
- Bachelor's degree
- Travel
Production Lead
Mello Farms —Amesbury, MA
- $22 - $25 an hour
- Full-time
- Basic math
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
2d
Retail Sales Print Production Lead (Seabrook, NH)
Staples, Inc. —Seabrook, NH
- Urgently hiring
- Management
- Computer literacy
- Mid-level
- Health insurance
- Dental insurance
Line Lead - Squares 2
Lindt & Spruengli (USA) Inc. —Stratham, NH
- $22.07 - $28.69 an hour
- Weekends as needed
- Background check
- Computer literacy
- Writing skills
Quick Apply
Production Team Lead
Spartronics Plaistow Inc —Plaistow, NH
- Overtime
- Computer literacy
- Mid-level
- High school diploma or GED
- Paid holidays
- Disability insurance
Quick Apply
Lead Production Technician
Analogic Corporation —Salem, NH
- Engineering
- 8 years
- Mentoring
Quick Apply
Print Production Lead - Full Time
Coastal Speedpro —Portsmouth, NH
- $18 - $25 an hour
- Full-time
- Mid-level
- Ability to lift 50 pounds
- Flatbed truck
- Health insurance
- Dental insurance
Quick Apply
4d
Ice Cream Shop Shift Lead / Production Associate (35 hrs/week)
Frozen Oasis LLC —Newington, NH
- $14 - $16 an hour
- Part-time
- Serving
- Cash register
- Bakery
- Employee discount
Quick Apply
Test Engineer Lead
Judit Inc —Wilmington, MA
- Engineering
- Travel
- Mentoring
Quick Apply
Low Rate Initial Production Systems Engineering Lead
Raytheon —Tewksbury, MA
- $132,400 - $251,600 a year
- Full-time
- Travel
- Senior level
- Leadership
- Paid holidays
- Disability insurance
Shift Lead (warehouse production) 1st shift
CHEP —Wilmington, MA
- From $23 an hour
- Overtime
- Hybrid work
- Computer literacy
- Mid-level
- Forklift
- Profit sharing
- Paid holidays
Quick Apply
Production Leader
Spartronics Plaistow Inc —Plaistow, NH
- Overtime
- Microsoft Outlook
- Mid-level
- High school diploma or GED
- Paid holidays
- Disability insurance
Quick Apply
Lead Quality Systems Specialist
Fresenius Medical Care —Lawrence, MA
- $94,700 - $157,000 a year
- Full-time
- Microsoft Access
- 6 years
- Microsoft Outlook
- Health insurance
- Dental insurance
Manufacturing Cell Leader - Aerospace and Defense Industry!
Ceco Concrete Construction, LLC —Exeter, NH
- Full-time
- Oracle
- Microsoft Outlook
- 5 years
- Paid parental leave
- Health insurance
12d
Warehouse Operations Lead
Maverick Tech —Wilmington, MA
- $24.66 - $39.56 an hour
- Full-time
- Mid-level
- Windows
- High school diploma or GED
Quick Apply
10d
Manufacturing Cell Leader - Aerospace and Defense Industry!
Costello April Design Inc —Exeter, NH
- Oracle
- Microsoft Outlook
- 5 years
- Paid parental leave
- Health insurance
Quick Apply
Patriot Program Quality Lead - Andover, MA
Raytheon —Andover, MA
- $68,900 - $131,100 a year
- Full-time
- Experience equivalent to degree accepted
- Senior level
- 2 years
- Paid holidays
- Disability insurance
8d
Lead Product Quality Engineer, Industrials
VulcanForms Inc. —Newburyport, MA
- $117,400 - $161,500 a year
- Full-time
- Engineering
- 8 years
- Travel
- Health insurance
- Dental insurance
Quick Apply
9d
Retail Sales Print Production Lead (Stratham, NH)
Staples, Inc. —Stratham Station, NH
- Urgently hiring
- Management
- Computer literacy
- Mid-level
- Health insurance
- Dental insurance
Test Lead
SubCom —Newington, NH
- Full-time
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Paid parental leave
- Health savings account
Quick Apply
3d

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production lead jobs near salisbury, ma

Quality Manufacturing Lead

SOFIE
Haverhill, MA

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Job Details

$90,000 a year

Qualifications

Customer complaint resolution

Full Job Description

Title | Quality Manufacturing Lead

Location | Haverhill, MA (MA1)

Department | Quality & Compliance

Reports To | Regional Manager, Quality Assurance (QA) (direct); Regional Director, Operations (dotted)

Compensation | $90,000

Quality Manufacturing Lead Overview

The Quality Manufacturing Lead supports the Quality Management System (QMS) at the SOFIE facility during daily manufacturing operations. The role reviews and releases product batch records as a qualified Quality Assurance (QA) representative, including primary and secondary reviews, as needed, and completes other QA activities to ensure product quality and regulatory compliance.

Key responsibilities are performed in real-time on the manufacturing floor during early production hours to provide quality oversight of the operations. This includes observing operations to prevent defects and quality events. Also, the role includes promptly initiating exception reports, escalating Customer/Product Nonconformance Reports (CPNRs) to the appropriate partners, and leading investigations, as needed. The Quality Manufacturing Lead serves as a key liaison between the Operations and Quality teams.

This role requires a professional with strong technical, quality, and operational knowledge, as well as an understanding of regulatory requirements and manufacturing realities. This balance enables practical, compliant recommendations and continuous improvements.

Essential Duties and Responsibilities

Ensure real-time process evaluation and confirmation of standard work by observing operations, learning processes, and preventing errors from propagating through the production flow.
Engage with operators through direct observation, encourage “first time right” execution, answer questions, participate in crisis management, and support other quality leadership initiatives.
Address process issues and inconsistencies through structured continuous improvement activities (e.g., kaizen events, root cause analysis) and update standard work instructions and SOPs accordingly.
Ensure real-time quality metrics, process performance indicators, and problem-solving boards are visible and maintained in production areas.
Ensure exception reports (Deviation, Out-of-Specification, No Yield, Atypical Production Investigations, etc.) are created promptly when events occur; initiate troubleshooting and investigations as required.
Ensure that investigations are performed and documented appropriately and that corrective and preventive actions are implemented in accordance with corporate CAPA, deviation, and OOS procedures.
Ensure team members are trained and authorized to identify, escalate, and participate in resolving quality issues; encourage operators to identify problems and stop processes when necessary to fix issues and foster a sense of ownership.
Verify that personnel are properly trained and qualified, and that all training records are accurately documented using the Absorb training platform.
Maintain oversight of all manufacturing and quality control records for GMP batches of PET drug products in accordance with 21 CFR Part 212.
Ensure components, containers, closures, in-process materials, packaging materials, labeling, and finished dosage forms are examined and approved prior to batch release.
Ensure manufacturing and analytical equipment are properly maintained and calibrated, and that applicable maintenance and system suitability activities are performed within intervals specified in equipment SOPs.
Notify management of issues related to personnel, equipment, or facility conditions that require corrective action.
Ensure deviations from standard procedures are documented and justified in batch records.
Ensure compliance with all applicable SOPs and regulatory requirements, including 21 CFR Part 212 (and Part 211, as applicable).
Apply QA processes and procedures to ensure consistent product quality and regulatory compliance.
Collaborate effectively with the Facility Manager and Operations team to support problem-solving and continuous improvement initiatives.
Review documents associated with the site QA program for completeness, accuracy, and compliance.
Write, review, approve, and implement procedures, specifications, processes, and methods as required.
Liaise with internal and external inspectors and representatives on QA-related topics.
Conduct ongoing review of aseptic operations to ensure compliance with internal procedures (e.g., gowning, cleaning, sanitation, sterility assurance, environmental monitoring) and USP/FDA regulations.
Ensure product complaints are managed in accordance with company SOPs and FDA requirements.
Open and manage change controls; initiate, maintain, and review SOFIE network and site-specific procedures related to assigned job functions.
Attend quality and operational meetings; interface with Corporate QA and Operations on quality-related issues and provide management with status updates as required.
Maintain extensive working knowledge of SOFIE products and quality processes.
Assist with quality review and approval of LIMS jobs prior to batch release.
Review and release product batch records as primary or secondary QA, as assigned.
Performance will be measured by defined organizational metrics.
Perform other duties as required.

Qualifications

Bachelor’s degree in a scientific, medical, or quality-related field preferred, or relevant experience.
Experience and/or comprehensive knowledge of manufacturing operations, sterile injectables preparation, aseptic processing, and aseptic product distribution preferred.
Previous experience in Quality, Pharmacy, or CGMP manufacturing environments preferred.
Working knowledge of USP, FDA, and cGMP regulations preferred.
Demonstrated ability to write, review, and revise SOPs.
Ability to read, analyze, and interpret governmental regulations, professional journals, and technical procedures.
Ability to interpret safety rules, operating and maintenance instructions, and procedure manuals.
Ability to write reports, business correspondence, and procedural documentation.
Ability to effectively present information, deliver training, and respond to questions from managers, operators, inspectors, customers, and stakeholders.
Strong analytical and problem-solving skills, including the ability to define problems, collect data, establish facts, and draw valid conclusions.
Proficiency in Microsoft Office applications.
Strong interpersonal and communication skills for interaction with site personnel, inspectors, and internal and external vendors.
Travel requirement: up to 10% domestically.

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Refine Your Search

production lead jobs in salisbury, ma

Quality Manufacturing Lead

Production Lead

Retail Sales Print Production Lead (Seabrook, NH)

Line Lead - Squares 2

Production Team Lead

Lead Production Technician

Print Production Lead - Full Time

Ice Cream Shop Shift Lead / Production Associate (35 hrs/week)

Test Engineer Lead

Low Rate Initial Production Systems Engineering Lead

Shift Lead (warehouse production) 1st shift

Production Leader

Lead Quality Systems Specialist

Manufacturing Cell Leader - Aerospace and Defense Industry!

Warehouse Operations Lead

Manufacturing Cell Leader - Aerospace and Defense Industry!

Patriot Program Quality Lead - Andover, MA

Lead Product Quality Engineer, Industrials

Retail Sales Print Production Lead (Stratham, NH)

Test Lead

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