Jobs in West Bridgewater, MA

Do you have 1 year of certified home health experience as an LPN? Are you looking for true flexibility when it comes to your career? If you’re nodding your head “yes”, you’re in the right place!

Weekday Pay Rate: $64.53 Per Point

Weekend Rate: $68.93 Per Point

Weekday availability preferred

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• W2 Employment
• ADP Workforce Now LifeMart Benefits
• Healthcare & 401k Eligibility

• Licensure: Current and unencumbered license as an LPN
• Experience: 1+ year(s) of Certified Home Health experience as an LPN
• Skills: Wound care, wound vac
• Availability: Must have reliable transportation, current driver's license, and car insurance coverage.
• Certifications: Current CPR certification; additional certifications in home health or geriatric care preferred.

• Provide independent, exceptional care to patients in their homes including comprehensive assessments and creating individualized care plans.
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Keywords: Licensed Practical Nurse, LPN, LPN Per Diem, Certified Home Health, HomeCare HomeBase, Side Hustle, Flexible Hours, Per Diem, Competitive Pay, PRN

Industry: Pharmaceuticals

Title: Quality Control Analyst III

Job ID: NORT000022

Location: Norton, MA

Duration: 10 months contract (+Possibility of extension)

This position is onsite and will be primarily located in Norton, MA. There may be occasional responsibilities at a secondary location in Cambridge, MA.

Overview

The Quality Control Operations (QCO) LEQ Analyst III plays a crucial role in supporting the department's efforts to maintain the highest standards of quality and compliance from development through to commercialization. This position is responsible for supporting and executing laboratory equipment qualification activities in compliance with USP and applicable regulatory requirements. This role ensures laboratory instruments are fit for intended use throughout their lifecycle and supports data integrity, compliance, and continuous improvement within the laboratory quality system. By ensuring these critical activities are executed with precision, the LEQ Analyst III significantly contributes to routine laboratory operations, thereby enhancing the overall efficiency and effectiveness of the QC functions .

Key Responsibilities (including but not limited to):

• Perform and support laboratory equipment qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) in accordance with USP .
• Classify laboratory instruments (Groups A, B, and C) and determine appropriate qualification strategies.
• Review and approve qualification protocols, test scripts, and reports.
• Support equipment lifecycle management, including calibration, maintenance, requalification, and change control.
• Review vendor documentation (URS, manuals, certificates) to support qualification and compliance.
• Investigate and document deviations, discrepancies, and out-of-tolerance events related to equipment performance.
• Ensure qualification activities comply with internal SOPs, cGMP, data integrity principles, and regulatory expectations (e.g., FDA, EMA).
• Collaborate with laboratory staff, quality assurance, validation, facilities, and vendors to resolve equipment-related issues.
• Maintain accurate and complete documentation in electronic quality systems.
• Support audits and inspections by providing qualification documentation and technical explanations as needed.
• Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance.
• Actively participate in continuous improvement efforts by identifying and suggesting enhancements to laboratory processes, particularly those related to efficiency and reliability.
• Actively participate in continuous improvement initiatives aimed at enhancing QC processes and procedures, increasing laboratory efficiency and effectiveness.

Qualifications

• B.S. in chemistry, biology, or biochemistry, or related scientific field ;
• Pharmaceutical/Biotech industry experience with 6-10 years in a GMP Quality Control function or equivalent, relevant industry experience
• Hands-on experience with laboratory equipment qualification in a regulated environment.
• Strong working knowledge of USP and laboratory instrument lifecycle management.
• Familiarity with cGMP, GLP, and data integrity requirements.
• Experience with common laboratory instruments (e.g., HPLC, GC, balances, dissolution, UV/Vis, pH meters, spectrometers).
• Ability to write clear, compliant technical documentation.
• Strong organizational skills with the ability to manage multiple tasks simultaneously and autonomously
• Excellent communication and teamwork abilities, capable of working effectively in a collaborative environment
• Experience in pharmaceutical, biotech, or contract testing laboratory environments.
• Exposure to computerized systems validation (CSV) as it relates to laboratory instruments.
• Familiarity with calibration and maintenance programs.
• Experience supporting regulatory inspections or internal audits.

Who We Are

IQE is a leading global supplier of compound semiconductor wafers and advanced materials. As one of the only compound semiconductor epitaxy foundries with worldwide presence and scalable manufacturing, IQE drives technology growth. Our vision is to be the top provider of advanced semiconductor materials by delivering exceptional quality, service, and innovation, making us the first choice for customers. Our strength comes from our diverse, expert workforce and a culture built on integrity, accountability, excellence, teamwork, and valuing people. At IQE, we are committed to reaching Net Zero and creating a sustainable future. We actively strive to reduce our carbon footprint, invest in green initiatives, and embed sustainability into everything we do. Join us in driving meaningful change and making a lasting impact on the environment

About the Role

The Production Supervisor role is responsible for the production of epitaxial materials as well as monitoring of the manufacturing process. This role focusses on the coordination and supervision of the Production team to ensure production processes run efficiently, safely and in compliance with quality standards.

Key Responsibilities

The Production Supervisor will be required to:

• Support a high level of cleanliness by completing scheduled housekeeping tasks.
• Comply with all company policies, SOP (Standard Operating Procedures), Work Instructions, and record keeping requirements.
• Comply with all EHS protocols and requirements.
• Comply with all health and safety, HR, environmental quality and cybersecurity guidelines and procedures internally and within the scope of business, ISO, and regulatory requirements as it pertains to the job function.
• Have clear understanding of chemicals and substances in the workplace and follow strict guidance for handling of such substances, which could include PPE requirements.
• Foster a collaborative work environment and promote teamwork across departments.
• The role may require a degree of flexibility in working hours, which will be discussed and agreed to support both individual and organizational needs.
• Split work between the cleanroom environment, following all required protocols and procedures and the office.
• Coordinate and supervise the daily activities of the Production team, setting priorities agreed with other cross-departmental supervisors.
• Establish programs and solutions for improved performance of operations equipment using Six Sigma or Lean Manufacturing tools.
• Lead projects and be accountable for ongoing objectives.
• Accountable for the documentation of safe working practices.
• Manages assigned team members and is responsible for the performance of the team.
• Conducts regular performance evaluations to provide consistent coaching and feedback.
• Have advanced experience and competence in the following:
• All manufacturing systems to carry out routine tasks accurately and efficiently.
• Have advanced experience and competence in ILM (In-Line metrology) tools with an understanding of application and operation.
• Scheduled routine calibration and monitoring tasks.
• Relevant manufacturing systems to follow and process routine tasks accurately, recording all works carried out for traceability.
• Have advanced understanding of wafer defects and continually monitor defects to reduce their occurrence.
• Instruct and mentor Operators and Technicians in various aspects of manufacturing process.
• Create and review all documentation to ensure accuracy, quality, as well as effectiveness of training.
• Supports continuous improvement initiatives.
• Have specialist experience and competence with troubleshooting.
• Liaise with other site functions to ensure daily targets are met.
• Be actively involved with the Emergency Response Team (ERT), providing feedback to the safety team on areas of improvement within the work environment.
• Perform other functions and duties as required.

About You

Experience Requirements for the Production Supervisor:

• Advanced experience in Production, Operations or equivalent manufacturing field.
• 6+ Years experience in Production, Operations or equivalent combination of education, experience and/or knowledge is desirable.
• Experience of working effectively in cross functional teams.
• Experience in supervising teams and effectively managing the performance of the team.

Qualification Requirements for the Production Supervisor:

• Qualification or 4-Year degree in relevant technical field or equivalent experience necessary to perform job responsibilities.
• Specialized technical or management qualifications relevant to the role.

Why should you join us?

All our employees benefit from:

• Long Term Incentive Plans (LTIPs)
• Professional Development and career pathways
• Market competitive base salaries reviewed bi-annually
• Comprehensive health insurance offering medical, prescription, dental and vision coverage.
• Company paid Life and Disability Insurance.
• Long service awards 5, 10, 15, 20, 25 and 30 years
• Values-based recognition awards
• Employee Assistance Program (Free family, legal, financial and counselling support 24/7 Access)
• 401k Plan with company match of up to 50% on the first 6% of the employee’s contributions

IQE is an equal opportunities employer that values diversity at all levels. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, or national origin.

Schedule

• Current Shift: 2nd shift (2:00 PM – 12:00 AM)
• Potential Change:
• May transition to 3rd shift (6:00 PM – 6:00 AM) mid-summer
• Rotating days using Pitman schedule (potentially Wednesday–Saturday)

Title: Manufacturing Contractor I

Duties:

With direct supervision this individual will perform routine clinical manufacturing operations at the Norton Manufacturing Facility, ensuring safe, efficient and cGMP-compliant operations at all times. Responsibilities include but are not limited to operation of production equipment in the areas of weigh/dispense, solution preparation, equipment CIP/COP and small parts cleaning, and materials stocking in manufacturing suites. Operates production equipment according to SOPs for the production of clinical products. Requires interaction with support groups (Facilities, QC, QA, Materials Management, EHS) to ensure accurate completion of activities.

Skills:

0-3 Years- Must possess mechanical and scientific aptitude and be able to clearly and thoroughly document all work on existing forms and records.

Biotech Certificate / 2 year degree and 1+ year of industry experience preferred.

Safety and the ability to maintain a compliant, highly effective and efficient product environment are critical.

High level of attention to details in both operations and documentation is required.

Must be able to execute strenuous, sometimes repetitive physical work on manufacturing shift schedule in classified cleanroom environment.

Ability to lift objects up to 50 lbs, and push/pull objects including bulk materials up to 250 lbs with assistance.

Ability to wear half face and full face respirators / PAPR as required for chemical processing.

Strong time management skills, attention to detail, and an ability to work in a team setting required. Excellent communication skills

Education:

Biotech Certificate / 2 year degree and 1+ year of industry experience preferred.

Position Status Label: Hourly Non-Exempt

The Axel Group is seeking a contract administrator on behalf of one of our clients located in the Bridgewater, Massachusetts area.

Job Title: Contract Administrator

Position Summary

The Contract Administrator is responsible for supporting the project management team with the preparation, review, tracking, and administration of contracts and related project documentation. This role ensures contractual compliance, maintains accurate records, and facilitates communication between internal teams, subcontractors, and vendors throughout the lifecycle of construction projects.

Key Responsibilities

• Prepare, review, and distribute subcontract agreements, purchase orders, and change orders.
• Track contract execution status and ensure all required documentation is received and properly filed.
• Maintain organized digital and physical contract files in accordance with company standards.
• Assist project managers with contract compliance, insurance certificates, bonds, and lien waivers.
• Support the change management process by tracking revisions, scope modifications, and approvals.
• Coordinate with accounting to ensure contract values align with budgets and payment applications.
• Monitor subcontractor documentation to ensure compliance with contractual and regulatory requirements.
• Assist in preparing reports related to contract status, commitments, and risk exposure.
• Respond to internal and external inquiries regarding contract terms and documentation.

Qualifications

• Bachelor’s degree in Construction Management, Business Administration, or related field preferred.
• 2–5 years of experience in construction administration, contract administration, or project coordination.
• Familiarity with construction contracts, subcontract agreements, and change order processes.
• Strong organizational skills and attention to detail.
• Proficiency in Microsoft Office Suite; experience with construction management software (e.g., Procore, Sage, or similar) preferred.
• Strong written and verbal communication skills.
• Ability to manage multiple projects and deadlines in a fast-paced environment.

Key Competencies

• Detail-oriented and process-driven
• Strong documentation and record-keeping skills
• Ability to work collaboratively with project teams
• Problem-solving and follow-through

Job Overview:

The Assistant Project Manager (APM) supports project execution from start to finish. This includes coordinating with vendors, subcontractors, and internal teams to ensure projects run efficiently and clients remain satisfied. The role reports directly to the VP | Project Executive.

The APM fosters a positive work ethic, motivates teams, and knows when to escalate issues to the Project Manager. They handle administrative, scheduling, and documentation tasks to support smooth project operations.

Primary Duties:

• Manage submittals and shop drawings.
• Participate in buy-out processes.
• Assist with RFIs, Proposed Change Orders, and meeting documentation (agendas, minutes).
• Handle commitment entries: contracts, purchase orders, change orders.
• Set up scopes of work for subcontractors and vendors.
• Assist in managing construction CPM schedules.
• Document project delays.
• Prepare schedule of values and draft payment applications for PM review.
• Assist with permitting and Certificate of Occupancy (C of O) processes.
• Procure materials and manage project closeouts (record drawings, O&M manuals, punch lists, inspections, warranties, commissioning).
• Perform periodic site visits.

Qualifications:

• Bachelor’s degree in Construction Management, Engineering, or related field (preferred).
• 1–3 years of construction APM experience.
• Proficient in Microsoft Office; MS Project and Procore experience recommended.
• Excellent written and verbal communication skills.
• Strong self-motivation, interpersonal, and project management skills.

Benefits:

• 401(k) & retirement plan
• Health, dental, and vision insurance
• Life & AD&D insurance
• Flexible spending and health savings accounts
• Paid time off
• Tuition reimbursement
• Referral program

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Flexible spending account
• Health insurance
• Life insurance
• Opportunities for advancement
• Paid time off
• Vision insurance

Work Location: In person

We are seeking a dedicated and experienced Commercial Landscape Construction Project Manager to oversee and manage commercial landscape construction projects from inception to completion. The ideal candidate will possess a strong background in landscaping, horticulture, and construction management, with the ability to lead teams effectively while ensuring high-quality standards are met. This role requires a blend of technical knowledge and leadership skills to deliver exceptional landscape solutions for our clients. Working knowledge of commercial roof top pedestals, pavers, amenities and planting is required.

Responsibilities:

• Manage all phases of landscape construction projects, ensuring they are completed on time and within budget.
• Supervise and coordinate the work of landscaping crews, providing guidance and support to ensure quality workmanship
• Collaborate with clients to understand their vision and requirements, translating them into actionable project plans.
• Conduct regular site inspections to monitor progress, quality, and safety compliance.
• Develop and maintain project schedules, budgets, and resource allocation plans.
• Ensure proper maintenance of equipment and tools used in landscaping projects.
• Provide training and mentorship to team members in landscaping techniques and best practices.

Requirements:

• Proven experience in Commercial landscape Construction
• Strong supervisory experience with the ability to lead diverse teams effectively.
• Excellent leadership skills with a focus on team development and performance improvement.
• Strong organizational skills with the ability to manage multiple projects simultaneously.
• Effective communication skills for interacting with clients, team members, and stakeholders.
• A valid driver's license is required

Job Type: Full-time/year 'round

Location: Greater New England Area

Experience Required: Minimum Degree in Construction Management, Engineering, or related field or 5 years in Site Work & Heavy Civil construction

Employment Type: Full-time

Benefits: Health, dental, vision, 401(k) with match, paid time off, life and disability insurance

Summary

We are seeking a detail-oriented and analytical Estimator to join our team. This role is responsible for preparing accurate cost estimates for complex projects by analyzing drawings, specifications, and other documentation. The ideal candidate has a strong understanding of all trades, site utilities, all types of earth support systems and contaminated soils. We are looking for a candidate that has experience in bidding work in Boston and outside of Boston with good communication skills. The ability to work collaboratively with project managers, vendors, and clients. This is a key position that supports competitive bidding and successful project execution.

Responsibilities

• Review of all documents, drawings, pricing, bonds, insurance and minority reporting
• Bid jobs contact subs for pricing on all scopes
• Scope reviews with general contractors
• Once awarded the project package together with project manager for in house kick off meeting
• Assist Project Manager, if needed, with full closeout of projects
• Estimate 1 – 2 jobs per week

Requirements

• Preferred degree in Construction Management or Engineering field
• Minimum 5 years’ office experience
• Minimum 5 years’ field experience
• Flexible with time commitment, possible weekend work
• Experience with CAD, Microsoft Project, Primavera, Construction Link, Excel, Agtek

Denommee Plumbing, HVAC & Electric is seeking an experienced Commercial MEP Estimator to join our dynamic team. If you have a passion for precision, experience in both engineered and design/build projects, and enjoy working across diverse commercial sectors — we want to hear from you!

What You’ll Do:

• Analyze drawings/specs for plumbing, HVAC, and electrical systems
• Prepare detailed cost estimates for labor, materials, and subcontractors
• Use FastEST, Trimble, Bluebeam, and ServiceTitan for estimating
• Collaborate with project managers and engineers to align scope and pricing
• Attend pre-bid meetings and site visits while working full-time in our Tyngsborough, MA office.
• Track bid schedules and ensure timely submissions

The Project Types You’ll Work On:

• Retail: Shopping centers, tenant fit-outs
• Hospitality: Hotels, restaurants
• Office/Mixed Use: Corporate buildings, multi-use developments
• Medical: Hospitals, clinics
• Government: Municipal buildings
• Education: Schools, universities
• Laboratory: Research facilities, clean rooms
• Manufacturing: Industrial plants, warehouses

What We are Looking for in a Candidate:

• 3–5+ years of commercial MEP estimating experience
• Strong knowledge of construction methods and codes
• Proficiency in FastEST and or other professional estimating tools
• Ability to read and interpret complex construction documents
• Excellent communication and organizational skills

What this Opportunity Offers:

• Competitive salary and benefits
• Career growth opportunities
• Supportive team culture that respects family life
• Exposure to high-impact, meaningful projects
• Access to industry-leading tools and tech

Ready to Build a Great Future?

Apply now by visiting the careers page on our website or message us directly to learn more!