Production manager jobs in Massachusetts - 1,097 jobs
Lead Dentist
Tend
Production manager job in Boston, MA
At Tend, we do dentistry differently - without compromising on excellence or ambition. As a Lead Dentist, you'll set the bar for clinical quality, mentor a high-performing team, and help shape the patient experience across your studio. You'll balance delivering best-in-class dentistry with leading and coaching dentists, hygienists, and dental assistants to excel clinically and professionally. Together with the Studio Manager, you'll create an environment that embraces Tend's Mission, Vision, and Values - and drives both patient and studio success.
We offer a guaranteed base plus a production bonus. Lead Dentists earn 32-40% of their adjusted production, making this one of the most competitive compensation models in the industry. You'll also receive leadership bonuses, transparency, and support to help you thrive.
What You'll Do
Clinical Leadership & Mentorship
Mentor and coach dentists, hygienists, and dental assistants in diagnosis, treatment planning, clinical skills, and patient care
Conduct regular performance reviews for general dentists; create action plans as needed
Partner with the Lead Hygienist and Lead Dental Assistant to provide team-wide mentorship and development
Lead clinical onboarding and quality assurance reviews for new hires
Ensure consistent delivery of high-quality care and patient experience across all providers
Studio Performance & Patient Care
Deliver comprehensive dentistry services at or above the standard of care, while modeling clinical excellence for your team
Partner with the Studio Manager to optimize schedules, improve patient access, and achieve production and care outcome goals
Lead daily pre-shift huddles and studio calibrations focused on workflow, patient care, and efficiency
Review and analyze clinical outcomes (e.g., REDOs, escalations) and implement solutions to continuously improve care
Take ownership of complex cases and coordinate member escalations, including making determinations on refunds and clinical resolution
Culture & Team Development
Build a collaborative, inclusive, and growth-oriented studio culture with your Studio Manager and clinical leads
Identify and nurture clinical team members with leadership potential
Participate in leadership development meetings and cascade key updates to your studio team
Model Tend's mission, vision, and values every day - and inspire others to do the same
Who You Are
You embody our Tend values and demonstrate advanced leadership competencies that ensure patient success, team excellence, and studio growth.
Tend Values
Tend to Others - Deliver outstanding oral health outcomes and patient experiences. You put the team and patient first, even in fast-paced settings.
Be Brave Enough to Lead - Act with integrity and take initiative to solve problems, coach others, and raise the bar.
Savor the Ride - Celebrate wins, stay resilient in challenging moments, and bring positivity to the workplace.
Embrace Our Differences - Welcome and value diverse backgrounds, ideas, and feedback. Communicate with respect and trust.
Rooted in Growth - Seek ongoing learning and improvement-for yourself and your team.
Role-Based Competencies
Earn and Give Trust - Earn the confidence of patients and teammates through honesty, transparency, and follow-through.
Lead with Clinical Judgement - Make sound clinical decisions grounded in data, evidence, and patient needs.
Empower Your Team - Set clear goals, delegate effectively, and help your team succeed.
What You Have
DDS or DMD degree from an accredited dental school
Current, active dental license in the state where you practice
Current CPR/BLS certification
Active DEA registration
Minimum 6 years of post-residency experience in private practice, DSO, or similar setting in a leadership role
Proven experience mentoring, teaching, or leading providers in a multi-chair environment
Demonstrated success managing complex patient cases and provider escalations
Comfort with modern technology and digital workflows (Invisalign certification strongly preferred)
Ability to work a full-time schedule of 4 days per week + 2 Saturdays per month
Physical Requirements
This position requires the ability to perform the essential job duties listed, with or without reasonable accommodation:
Ability to sit and stand for extended periods while performing clinical procedures.
Manual dexterity and fine motor skills to handle dental instruments and perform precise procedures.
Adequate vision (with or without correction) to read charts, interpret radiographs, and operate clinical equipment.
Ability to bend, reach, and maintain ergonomic positioning for patient care.
Occasional lifting or movement of equipment and supplies up to 25 pounds.
Ability to communicate effectively with patients, team members, and other healthcare professionals in person and via technology.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role.
What We Offer
Dentist Equity & Partnership - Opportunity to invest alongside Tend and benefit from our growth
CE & Professional Development - Virtual and in-person CE opportunities and internal clinical forums
Time to Recharge - Enjoy generous Paid Time Off (PTO) and company holidays - because rest is productive.
Malpractice Insurance - Full coverage provided at no cost to you
Health Comes First - Medical, dental, and vision insurance - plus our own Dental Wellness Program
Plan for the Future - 401(k) with company match
Support, When You Need It - Life & AD&D insurance, legal support, EAP, and health advocacy
Smart Spending Options - FSAs, HSAs, and pre-tax transit and parking benefits
Generous paid time off + company holidays
#LI-Onsite
Pay Range
$194,000-$350,000 USD
The Tend Difference
The highest standard of care, anywhere.
At Tend, you'll work alongside esteemed clinical leaders and experience-obsessed colleagues to deliver care that's not only top-tier - it's unforgettable. With access to advanced technology and thoughtfully designed studios, you'll help create dental experiences that patients actually look forward to. Our hospitality-driven approach makes every visit feel personal, warm, and empowering.
A top-tier clinical team who puts patients first.
We value science over sales and lead with empathy, transparency, and integrity. There are no production quotas here - just a shared commitment to doing what's right for our patients. We foster a collaborative, inclusive culture where team members go the extra mile for each other and for every patient who walks through our doors.
Innovate Dentistry. Tend to Others. Grow Together.
Tend is redefining what it means to grow a career in dentistry. We offer a modern, patient-first environment backed by cutting-edge tools and systems, industry-leading compensation and benefits, and robust opportunities for continuing education and professional development. Whether you're clinical or corporate, you'll be part of something meaningful - and surrounded by people who care.
Tend is an Equal Opportunity Employer.
We're committed to fostering a workplace where everyone feels seen, heard, and supported. Tend does not discriminate based on race, color, religion, sex, national origin, age, disability, genetics, gender identity or expression, sexual orientation, veteran status, or any other protected status in accordance with applicable federal, state, and local laws. This policy applies to all aspects of employment, including recruitment, hiring, promotion, compensation, benefits, and termination.
Legal and Compliance Notice:
Tend complies with all applicable federal, state, and local laws governing nondiscrimination, equal employment opportunity, pay transparency, and other employment-related requirements. Where specific state disclosures or postings are required by law, we provide this information as part of our hiring process or upon request.
Your privacy matters.
To learn more about how we collect, use, and protect your information, please review our privacy policy here.
$82k-133k yearly est. 4d ago
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General Manager, SPARC Plant
Fusion Energy Base
Production manager job in Massachusetts
About Commonwealth Fusion Systems
Commonwealth Fusion Systems is on a mission to deliver the urgent transition to fusion energy.
Combining decades of research, top talent, and new technologies, we're designing and building commercially viable fusion power plants. And working with policymakers and suppliers to build the energy industry of the future.
We're in the best position to make it happen. Since 2018, we've raised nearly $3 billion in capital, making us the largest and leading private fusion company in the world.
Now we're looking for more thinkers, doers, builders, and makers to join us. People who'll bring new perspectives, solve tough problems, and thrive as part of a team.
If that's you and this role fits, we want to hear from you.
Join the power movement as General Manager, SPARC Plant
This leadership role has the mandate to run our first-of-a-kind SPARC facility, ensuring its ultimate success. You will be responsible for maximizing facility uptime and scientific learning, building and leading the world-class team that operates SPARC, and shaping a culture of excellence and innovation. This is a unique opportunity to lead the facility that will prove commercial fusion energy is achievable and change the world. This role reports to the CEO.
What you'll do
Oversee all aspects of the SPARC Plant to ensure maximum uptime, operational readiness, and scientific productivity
Lead, build, and mentor the entire SPARC Plant team, setting a tone for a positive, collaborative, and high-performance culture
Collaborate with senior leadership across CFS to understand company priorities and ensure plant operations directly support overall strategic needs
Develop and manage the plant's budget and staffing plans, deploying resources for maximum productivity and success
Establish and continuously improve processes and systems to ensure the safe, efficient, and effective operation of a complex, first-of-a-kind fusion facility
Serve as a key interface between the SPARC Plant team and other leaders within CFS
Work with the Open Innovation team to support strategic interactions with the external scientific community and other stakeholders
What we're looking for
Bachelor's degree in Engineering (e.g., Mechanical, Electrical, Nuclear), Physics, or a related technical field
15+ years of progressive experience, with at least 8-10 years in a senior leadership role managing a complex, high-consequence technical facility (e.g., power plant, national laboratory, semiconductor fab, large-scale manufacturing). This includes a demonstrated ability to lead and manage a team of at least 200+ employees, including a mix of direct reports and managers
Extensive experience operating and maintaining large process systems, including but not limited to chemicals, cryogenics, oil/gas, or similar large-scale infrastructure
Robust technical knowledge of complex processes and electrical systems common in large facilities
Directed a $500M plus lab or research effort, from its initial scientific concept and development to the final construction and operational launch
Proven track record of building, leading, and mentoring high-performing technical and operational teams
Demonstrated experience in operational excellence, including developing and implementing novel processes, managing large budgets, and strategic resource planning
Exceptional leadership and communication skills, with the ability to inspire a team and articulate complex technical and strategic concepts to a wide variety of audiences
Strong people management skills of both small and large teams
Leadership, team-building, and mentoring skills for both engineers and technicians
Demonstration of the ability to build trust with front line employees and identify issues first hand
Ability to adapt to a rapidly changing environment
Strong attention to safety and the creation of a safety culture
Bonus points for
Master's, PhD, or MBA
Experience with the commissioning and operation of first-of-a-kind systems or facilities is strongly preferred
Must-have requirements
Perform activities such as typing or sitting for extended periods of time
Willingness to occasionally travel or work required nights/weekends/on-call
Work in a facility that contains industrial hazards including heat, cold, noise, fumes, strong magnets, lead (Pb), high voltage, high current, pressure systems, and cryogenics
$275,000 - $350,000 a year
Salary range for this full-time position + equity + benefits
The actual salary will depend on level, location, qualifications, and experience. The range displayed on each job posting reflects new hire salaries for the position across all US locations. Benefits include:
Competitive compensation with equity
12.5 Company-wide Holidays
Flexible vacation days
10 sick days
Generous parental leave policy
Health, dental, and vision insurance
401(k) with employer matching
Professional growth opportunities
Team-building activities
LI-Hybrid
At CFS, we excel in fast-paced environments, driven by our values of integrity, execution, impact, and self-critique. As we grow, we're eager to bring on mission-driven folks who offer diverse perspectives and fresh ways to tackle challenges.
We value diversity deeply and are proud to be an equal opportunity employer by choice. We consider all qualified applicants equally, regardless of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law.
This role requires compliance with U.S. laws concerning the export of controlled or protected technologies or information (collectively, “Export Control Laws"). Any offer of employment will be contingent on the need for compliance with such Export Control Laws.
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$87k-140k yearly est. 3d ago
AM Senior Bakery Production Manager
Tatte Bakery 3.7
Production manager job in Boston, MA
Boston Bakery, 60 Old Colony Ave, Boston, MA 02127, USA
The AM Senior Bakery ProductionManager's primary responsibility is to oversee all first shift baking and production at our modern‑manufacturing facility. The AM Senior Bakery ProductionManager is committed to uncompromising quality and craftsmanship in all aspects of our production and is responsible for ensuring that all products are prepared to Tatte specifications and ensures morning production is on time and consistent with relevant safety protocols and regulations. Additionally, a Senior AM Bakery ProductionManager supports bakery leadership in areas including but not limited to customer service, food safety, inventory management systems and compliance with all Tatte policies as well as local and government regulations. This person is responsible for our equipment and for cultivating a safe work environment for all employees by maintaining high standards of cleanliness and food safety.
Summary of Responsibilities
Ensuring consistent and quality products per Tatte procedures and specifications
Scheduling team members and timely posting of team member schedules
Directing the daytime production team to execute all production tasks efficiently, effectively, and safely
Being responsible for the quality control process in producing, baking, finishing, picking, and packaging all goods, ensuring products are up to Tatte standards
Maintains safety, sanitation, and cleanliness standards (Tatte, Local, State and Federal) of the entire premise, including sharing the responsibility of local and federal food inspections along with the Department of Transportation guidelines
Responsible for first shift staff in the bakery, including adequate staffing, onboarding, managing, developing, and accountability protocols for all hourly bakery team members. This also includes a commitment to the safety and well-being of all employees.
In partnership with the General Manager and bakery leadership team, assists with production and operational planning, including effectively and efficiently managing labor expenses and waste
Maintains strong and effective relationships with all bakery & café managers
Promotes, models, and maintains Tatte culture and adheres to all Tatte policies
Active involvement in ongoing evaluation and development of team members
Actively participates in management meetings to ensure effective and accurate communication of all relevant product and operational information
Understands and follows crisis management procedures
Other duties, as assigned
Working Conditions / Essential Functions
Able to stand for 10 hours per shift/day, 5-days a week for an average workweek of 50 hours
Able to grasp, reach overhead, push, lift and carry up to 50 pounds
Must be available to work morning shifts during the week and weekend, and holidays (as needed)
Position Requirements
5+ years managerial experience in a high-volume baking or other food production facility
Ability or a willingness to learn to operate bakery manufacturing equipment such as deck ovens, proofers, rack ovens, fryers, etc.
Ability to multi-task in a fast‑paced, high‑volume production bakery
Ability to direct and manage a team of bakers through kind and empathetic leadership
Other Preferred Skills
Familiar with Good Manufacturing Practices
Experience building and mentoring high performance teams
Fluency in Spanish and English
Our Benefits and Perks
Competitive pay (ranging from $85-100k, depending on experience)
401(k) (with a vesting match)
Free EAP employee assistance programs
Paid vacation time (after three months of full‑time service)
Immigration Reimbursement Program (after one year of full‑time service)
Health, dental and vision insurance
Generously discounted meals and free drinks
Exciting potential for growth
Please note that Tatte is an E‑Verify employer.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.
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$85k-100k yearly 1d ago
Strategic BioPharma Partnerships Lead - Precision Oncology
Precede Biosciences
Production manager job in Boston, MA
A biotechnology company in Boston seeks a Director of Business Development to lead efforts in advancing partnerships with biopharmaceutical companies. This role requires an advanced degree and 7-10 years of experience in business development. The director will manage key relationships, negotiate partnerships, and drive value creation. The salary range is $220,000 - $250,000 annually, with potential bonus and equity options.
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$220k-250k yearly 4d ago
WWTP Operations Lead Team
Mentor Technical Group 4.7
Production manager job in Boston, MA
Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
SUMMARY
Responsible for defining, planning, developing, executing, and monitoring the proposed scope of work for the administration and operation of the laboratory, “limited maintenance,” and operations of the advanced wastewater treatment systems. Responsible for defining and negotiating strategies and programs related to wastewater treatment operations in accordance with the operational contract, ensuring compliance with client expectations and/or goals as well as regulatory requirements.
Creates, through leadership and results, a culture of safe and advanced operations that integrates all elements of operational excellence. Monitors advanced treatment processes and implements and executes continuous improvement initiatives for wastewater treatment operations. Influences clients to prioritize work plans and ensures total customer satisfaction in a cost-effective manner.
At times, and when required, may operate, control, monitor, and maintain the wastewater treatment system, which includes: effluent pumping systems, aerobic and anaerobic treatment systems, biogas treatment system (Thiopaq), laboratory area, solids separation (“Decanters”), biogas burning flares, softener systems, receiving and/or movement of production materials, and general (limited) maintenance, as required by the process.
REQUIREMENTS Education
Bachelor's or master's degree in Environmental Engineering or Chemical Engineering.
Experience
Experience in the field of Environmental or Chemical Engineering, with emphasis on design, construction, operation, and/or maintenance of wastewater treatment systems; or equivalent management and supervisory experience in industrial or consulting roles within Quality, Environmental, and Occupational Safety Programs, with a record of excellence.
Additional Requirements
Wastewater Treatment Plant Operator License - Category IV (for treatment plant) (preferred)
EIT and/or Engineer License from the Puerto Rico Department of State; CIAPR credentials (preferred)
Experience in Project Management (PMI) of advanced treatment systems
Knowledge in the operation and maintenance of systems through computerized controls (PLCs, HMIs, PCs, etc.)
Bilingual (English/Spanish)
Willing to work in shifts (7 days/24 hours), overtime, and during emergencies as required
Must observe and promote compliance with company safety rules, reporting any violation or deviation to the immediate supervisor
Work may be performed indoors and outdoors, occasionally at heights. Exposed to temperature changes, occasional heat, wet areas, high and low humidity, noise, and vibrations.
Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.
Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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$112k-148k yearly est. 2d ago
Packaging Manager
Pharmaceutical Manufacturing
Production manager job in Fall River, MA
Job Title: Packaging Manager - Inhalation / MDI (Pharmaceutical Manufacturing)
Work Schedule: General: 8:30 AM - 5:00 PM (May vary based on business needs; shift flexibility required)
Employment Type: Full-Time | Exempt (Professional)
Salary Range: (Based on Experience) (Relocation support may be available)
Position Overview
We are seeking an experienced Packaging Manager - Inhalation/MDI to lead and manage pharmaceutical packaging operations in a cGMP-regulated manufacturing environment. This role is critical in ensuring safe, compliant, and on-time packaging of Metered Dose Inhaler (MDI) products, while driving operational excellence, team development, and continuous improvement.
This is a hands-on people manager role, not a desk-based position.
Key Responsibilities
📦 Packaging Operations & Production
Plan, monitor, and control daily packaging activities to meet production targets, quality standards, and timelines
Review planned vs. actual production and adjust schedules as required
Ensure availability of packaging materials, components, consumables, and spare parts across all shifts
Drive execution of new product introductions and technology transfers through gap analysis
Optimize utilization of packaging equipment, consumables, and manpower
🧪 Quality, Compliance & cGMP
Ensure all packaging activities comply with cGMP, safety, and regulatory requirements
Review in-process controls and packaging documentation to ensure right-first-time execution
Lead and support investigations including deviations, OOS, OOT, complaints, and CAPAs
Prepare, review, and maintain SOPs, BMRs, APQRs, validation, and qualification documents
Support internal, external, and regulatory audits (including USFDA inspections)
⚙️ Equipment, Engineering & Continuous Improvement
Coordinate with Engineering and Maintenance for preventive maintenance and breakdown resolution
Monitor OEE / OOE data and implement PDCA-based improvements
Drive packaging excellence initiatives to improve yield, reduce downtime, and minimize losses
Identify bottlenecks and develop capacity utilization plans
👥 People Management & Safety
Lead, train, and manage packaging teams across multiple shifts (15 direct / ~45 total staff)
Ensure adequate staffing, shift planning, and effective manpower utilization
Train teams on SOPs, GMP, safety, and new processes
Promote a strong safety culture; ensure PPE compliance and safe work practices
🔹 Education & Experience
🎓 Education
Bachelor's degree in Pharmaceutical Manufacturing, Industrial Engineering, or related discipline preferred
🏭 Experience
5-9 years of pharmaceutical packaging experience in a cGMP environment
Minimum 3+ years in a supervisory or managerial role
Hands-on experience with MDI (Inhalation) packaging lines is required
Direct exposure to USFDA and regulatory audits
Experience with SAP and manufacturing systems is a plus
Required Competencies
Strong knowledge of pharmaceutical packaging operations and MDI products
Expertise in GMP documentation and compliance
Proven troubleshooting, investigation, and root cause analysis skills
Effective leadership, communication, and cross-functional collaboration
Comfortable working in a fast-paced, regulated manufacturing environment
Working Conditions
Onsite role in a pharmaceutical manufacturing environment
PPE required (gowning, safety equipment, respiratory protection as applicable)
Shift flexibility, including occasional weekends or holidays based on business needs
No remote work available
$91k-150k yearly est. 14h ago
Production Supervisor
Novax Recruitment Group
Production manager job in Lowell, MA
📌 Production Supervisor - Steel Fabrication
📍 Lowell, Massachusetts
💰 Compensation: $75-115,000
🚀 Why This Role Matters
Lead a skilled production team manufacturing custom steel components for large-scale construction projects. You'll ensure schedules, safety, and quality standards are met while keeping operations efficient and teams motivated. Your leadership drives performance and product excellence.
🎯 Key Responsibilities
Oversee daily fabrication operations and production flow
Manage and motivate shop personnel to meet safety, quality, and output goals
Coordinate materials, equipment, and workforce to minimize downtime
Track performance metrics and report on production progress
Support hiring, training, and performance evaluations
Ensure compliance with all safety and quality requirements
✅ Ideal Candidate Profile
5+ years' experience in steel fabrication, manufacturing, or related industry
Proven leadership experience in a supervisory or lead role
Strong blueprint reading and production planning skills
Excellent communication and organizational abilities
Safety-focused mindset with a commitment to continuous improvement
📨 How to Apply
Submit your resume and cover letter to ************************** or apply online.
$75k-115k yearly 14h ago
Production Supervisor
JVT Advisors 3.7
Production manager job in Rochester, MA
Production Supervisor needed to lead a team of roughly 7-12 employees in Rochester, MA. Company is in growth mode looking for someone who desires long-term employment and career growth.
Salary Range: $115K-$120K, health insurance with an HRA, dental, vision, LTD, and a 401(k) retirement plan with an employer match. 3 weeks PTO, 1 week sick. Generous relocation package offered. Qualified candidates are encouraged to apply.
Company Overview
A leading precast concrete supplier in MA and NH with 50+ years of experience, providing high-quality products such as septic tanks, manholes, drainage structures, curbing, steps, and retaining walls. Serves engineers, contractors, and homeowners with a focus on performance and customer service.
Position Summary
Lead and supervise production operations in a precast concrete facility.
Support the Plant Manager in ensuring safety, quality, and compliance with regulations.
Coordinate work activities and resources for efficient, high-quality output.
Responsibilities
Oversee and participate in the production of concrete products.
Delegate tasks and ensure adherence to safety policies and quality standards.
Coordinate schedules and set production priorities with the Plant Manager.
Drive continuous improvement to boost efficiency and reduce costs.
Maintain and track equipment maintenance and requisitions for supplies.
Manage hiring, training, and evaluation of production staff.
Prepare incident reports and ensure a clean, safe work environment.
Attend management meetings and stay current with NPCA PQS courses.
Encourage employee engagement and improvement programs.
Minimum Qualifications
5+ years' experience in precast manufacturing.
Strong self-starter with energy and results orientation.
Knowledge of quality systems, health & safety compliance, and production tools.
Ability to read blueprints and apply math concepts.
Proficient in MS Word, Excel, and general computer skills.
Strong communication and leadership skills.
Valid driver's license.
PQS1 and ACI certifications preferred.
Supervisory Responsibilities
Assist the Plant Manager in supervising production employees.
Serve as Acting Plant Manager in their absence.
Key Competencies
Teamwork and collaboration
Critical thinking and decision-making
Time management and organization
Delegation and coordination
Conflict resolution and stress tolerance
Work Environment & Physical Demands
Industrial plant setting.
Frequent climbing, lifting, walking, and handling materials.
Ability to lift/carry up to 50 lbs and work at heights up to 10 ft.
Must wear proper PPE at all times.
$115k-120k yearly 14h ago
External Scientific Partnerships Lead - Rare Diseases (Equity Eligible)
Astrazeneca GmbH 4.6
Production manager job in Boston, MA
A leading pharmaceutical company is seeking an Associate Director for External Scientific Partnerships to develop strategic initiatives with health professional societies. The ideal candidate should hold a PhD, PharmD, or equivalent and have 3-5 years of experience in the pharmaceutical field, particularly in rare disease. This role entails fostering key partnerships and engaging with thought leaders to advance medical strategies. Competitive compensation and benefits are offered, including an annual salary ranging from $150,202 to $225,304.
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$150.2k-225.3k yearly 4d ago
Bioconjugation GMP Manufacturing Supervisor
Veranova
Production manager job in Devens, MA
Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.
Role Overview:
Veranova is seeking a highly motivated, adaptable, and experienced Supervisor to support its new state-of-the-art single-use DS biologics manufacturing facility in Devens, MA, and to integrate this operation with existing cGMP manufacturing activities. In this role, you will oversee the systems, teams, and processes required to enable clinical manufacturing and future commercial launches. This is a unique opportunity to help shape the future of the Devens site as it expands into bioconjugate manufacturing, building on its strong foundation in process development and in clinical and commercial production of linker-payloads for global pharmaceutical partners.
Core Responsibilities:
Distribution of responsibilities across multiple workstreams within the GMP manufacturing asset. Drive prioritization and sequencing of workstreams within a client process to achieve results consistent with process design. Align operational and project timelines, deliverables and resources
Evaluate industry's best practices and select an appropriate program and project delivery that supports the dynamic nature of a new facility startup and integrates with existing governance and delivery frameworks
Manage the tools, standards, business processes, documentation, metrics and communication associated with operational GMP facility
Organize , prioritize, sequence and track contract manufacturing projects in cGMP facility
Manage staff of operations personnel assure training and batch record execution to achieve successful project execution
Additional assignments/ duties to support team objective and contribute to the Veranova mission may evolve based on business needs
Qualifications:
Required
Bachelor's degree in engineering, life sciences or related field and 7-10 years of experience in biotech/pharma manufacturing or process development with a minimum of 2 years direct people leadership experience
Master's degree in engineering, life sciences or related field and 5+ years of experience in biotech/pharma manufacturing or process development with a minimum of 2 years of direct people leadership experience
Strong understanding of cGMP compliance
Proven experience managing project timelines for delivery of client drug substance
Demonstrated ability to thrive in a dynamic environment and collaborate across diverse technical areas
Preferred
Experience with biological drug substance manufacturing equipment and processes, single-use equipment technologies, and cGMP facility qualification and startup
Salary Range : $105,000 - $125,000 annual base salary
Our Commitment:
Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.
Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don't meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .
$105k-125k yearly 4d ago
Strategic Advisory Leader, Life Sciences Growth
Trinity Partners
Production manager job in Waltham, MA
A leading strategic advisory firm in Waltham, MA, is seeking a Partner to drive business growth, enhance client relationships, and lead staff development. The ideal candidate will be responsible for generating $3 to $5 million in annual revenue and will provide intellectual leadership within the firm. This leadership role requires a strong network in the pharma and biotech industries, along with excellent project management skills, making it crucial to ensure successful client engagements and talent growth.
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$82k-133k yearly est. 5d ago
Strategic Leader, Commercial Insights & Analytics
Zenasbio
Production manager job in Waltham, MA
A biopharmaceutical company located in Waltham, MA is seeking a Senior Director for Commercial Insights and Analytics. This role is critical in evaluating market landscapes and providing strategic insights to commercial teams. The ideal candidate will possess at least 10 years of experience in the pharmaceutical industry and hold a Bachelor's degree in a relevant field. Responsibilities include conducting market research, delivering insights, and supporting commercial initiatives in a hybrid work environment. A competitive compensation package is offered.
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$82k-133k yearly est. 2d ago
Wastewater Market Sector Leader - New England Growth
Fashion Institute of Design & Merchandising
Production manager job in Boston, MA
A leading engineering and design firm is looking for a New England Wastewater Market Sector Lead with over 15 years of experience in wastewater planning, design, and construction. You will manage projects, lead strategic initiatives, and drive business development in the wastewater market across New England. Ideal candidates will have strong client relationships and a proven track record in wastewater treatment systems. This is a full-time position based in Boston, Massachusetts, with a collaborative team focused on sustainable water solutions.
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$82k-133k yearly est. 5d ago
East Health Market Leader - Growth & Strategy
Cannondesign
Production manager job in Boston, MA
A leading design firm is seeking a Regional Market Leader for the health sector located in Boston, Massachusetts. This role requires a seasoned leader to develop strategies, manage client relationships, and ensure the overall growth of the regional market. Responsibilities include leading diverse teams, strategic positioning, and direct engagement with top-tier clients to enhance brand visibility. The ideal candidate will have extensive experience in business development and a strong commitment to Living-Centered Design principles. Competitive salary range is offered along with a comprehensive benefits package.
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$82k-133k yearly est. 4d ago
Athletics Compliance Leader - NCAA DI & Policy
Merrimack College Federal Cu 4.0
Production manager job in Boston, MA
A prominent educational institution is seeking an Associate Athletic Director for Compliance. This role involves overseeing NCAA compliance programs and ensuring all coaches and student-athletes adhere to collegiate regulations. The ideal candidate will have strong leadership and communication abilities, with a demonstrated understanding of NCAA rules. Responsibilities include managing compliance policies and liaising with various departments to ensure adherence to regulations. The position offers the opportunity to work in a dynamic environment within the college athletics framework.
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$95k-123k yearly est. 3d ago
Production Print & Device Fleet Specialist
Xerox AG
Production manager job in Boston, MA
A global technology leader is seeking a Print/Mail/Scan Associate in Boston to manage equipment fleets and provide on-site support. The ideal candidate has experience in print technology and MFDs, with skills in networking and troubleshooting. Responsibilities include monitoring device performance, handling service requests, and executing printing tasks. Competitive compensation, comprehensive benefits, and a focus on work-life balance are offered.
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$32k-50k yearly est. 2d ago
Oncology Imaging & Biomarker Strategy Lead
Regeneron Pharmaceuticals, Inc. 4.9
Production manager job in Boston, MA
A leading biotechnology firm is seeking a Clinical Imaging Scientific Director for Oncology to lead imaging strategy and execution in clinical trials. The ideal candidate will have a PhD and over 10 years of experience in clinical imaging, particularly in oncology, with significant expertise in PET imaging and regulatory engagement. This role requires collaboration with research teams and overseeing imaging project implementation, contributing significantly to oncology drug development. Comprehensive benefits are offered to eligible employees.
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$104k-139k yearly est. 3d ago
Strategic Advancement Leader - Major Gifts & Campaigns
Winsor School 4.2
Production manager job in Boston, MA
A prestigious independent school in Boston is seeking a Chief Advancement Officer to lead its comprehensive advancement program. This role includes managing fundraising initiatives, engaging with major donors, and mentoring a team of advancement professionals. The ideal candidate will have over 10 years of experience in a similar capacity within education or non-profit sectors, a strong track record in fundraising operations, and excellent communication and strategic planning skills. A competitive salary and benefits package is offered.
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$53k-78k yearly est. 4d ago
Autonomous Vehicle Operations Supervisor
Aceolution
Production manager job in Boston, MA
Role: Autonomous Vehicle Operations Supervisor
No of positions Open: 3
The AV Supervisor will oversee daily operational activities for the Autonomous Vehicle (AV) Drive Operations Program across designated city sites. This role ensures smooth field operations, compliance with safety standards, quality of service delivery, and team performance. The AV Supervisor will work closely with local and regional leaders to ensure efficient deployment of AV fleets and consistent driver/operator management.
Key Responsibilities
Lead, coordinate, and supervise AV Driver/Operator teams across assigned locations.
Conduct daily shift planning, scheduling, task delegation, and attendance tracking.
Ensure compliance with all safety, security, and operational protocols.
Train, coach, and mentor new and existing AV operators on operational procedures and program standards.
Conduct performance reviews, provide feedback, and manage disciplinary actions when required.
Collaborate with cross-functional teams (Operations, Fleet, Safety, Engineering) to ensure vehicle readiness and resolve operational issues.
Monitor site productivity metrics and implement improvements to enhance efficiency.
Respond to on-ground escalations and operational emergencies promptly.
Prepare weekly operational status reports and performance summaries.
Coordinate with Fleet & Maintenance teams to ensure optimal vehicle uptime.
Travel between Tampa, Baltimore, and Pittsburgh as operational needs require.
Qualifications
3+ years of experience in Operations, Transportation, Logistics, Automotive, or related field.
Prior experience in a supervisory or lead role managing teams.
Strong understanding of safety protocols and compliance-driven environments.
Excellent communication, leadership, and people management skills.
Ability to analyze performance metrics and identify process improvement opportunities.
Comfortable working in dynamic and fast-paced field settings.
Valid driver's license with a clean driving record.
Ability to travel between assigned cities as needed.
Preferred Skills
Experience working with autonomous vehicles, fleet operations, or mobility transportation programs.
Knowledge of incident reporting, compliance documentation, and operational audits.
Technical aptitude to understand basic AV system operations and diagnostics
Work Environment
On-site operations environment; may require early mornings, late evenings, weekends, or split shifts based on program schedules.
Field-based work involving both indoor and outdoor environments.
Significant travel required - approximately 90% of the time across locations.
$46k-78k yearly est. 14h ago
Central Processing Supervisor, Core Laboratory
Brine Group
Production manager job in Boston, MA
Central Processing Supervisor, Core Laboratory - Evening Shift
Evening Shift: 3p - 11:30p ($3/hr evening diff).
Must be ASCP certified (or equivalent).
Sign-on bonus eligible.
Responsibilities:
Responsible for coordinating the daily operation of the front office of the core laboratory.
Oversees all Pre and Post analytic activity on the evening shift, in close conjunction with the day shift MT Operations Coordinator, reference lab staff, and other individuals who oversee areas that have an overlapping operating relationship with Central Processing.
Ensures that all activities, processes and policies are carried out in strict compliance with governmental regulations, licensing agency standards, and hospital policies and procedures.
Responsible for day-to-day general management including staffing, schedules, payroll, performance management, training, education, development of policy and protocol, compliance, and safety.
FTE's: 25+/-.
Reports to the Technical Director of Pre/Post Analytics in the Core Laboratory.
Qualifications:
MT (ASCP) or equivalent.
Bachelor's Degree in Medical Technology or physical sciences.
4+ years of hospital laboratory experience, including knowledge of &/or experience with pre/post analytics &/or central processing.
1+ years of leadership experience.
Preferred: experience overseeing non-exempt hourly staff.