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Process Control Manager Jobs in Charlestown, MA (NOW HIRING)

TransMedics

Manager Quality Control

Andover, MA · On-site

Manage inspectors and inspection processes of medical devices. (1st shift) * Carry out supervisory ... Ensure the Quality Control department complies with 21CFR820, ISO 13485, MDSAP and MDR

TransMedics

Manager Quality Control

Andover, MA · On-site

Manage inspectors and inspection processes of medical devices. (1st shift) * Carry out supervisory ... Ensure the Quality Control department complies with 21CFR820, ISO 13485, MDSAP and MDR

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

Regulatory Compliance, cGMP, Statistical Process Control * Extensive analytical chemistry experience * Project management * Data collection, management and analysis * Ability to direct and be ...

PM Group

Lead Process Engineer

Boston, MA · On-site

$120K - $160K/yr

Support asset onboarding, calibration programs, preventive maintenance planning, and spare parts management. * Coordinate integration activities with automation, process control systems, digital ...

PM Group

Lead Process Engineer

Boston, MA

$120K - $160K/yr

Support asset onboarding, calibration programs, preventive maintenance planning, and spare parts management. * Coordinate integration activities with automation, process control systems, digital ...

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All JobsProcess Control JobsProcess Control Manager JobsProcess Control Manager Jobs in Charlestown, MA

Process Control Manager information

See Charlestown, MA salary details

$40.8K

$109.8K

$151.2K

How much do process control manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for process control manager in Charlestown, MA is $109,784.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,900.00 and $122,900.00 per year, depending on experience, location, and employer.

What is the difference between Process Control Manager vs Process Engineer?

AspectProcess Control ManagerProcess Engineer
CredentialsBachelor's degree in engineering, certifications in process control (e.g., Certified Control Systems Technician)Bachelor's or master's in chemical, mechanical, or industrial engineering; certifications vary
Work EnvironmentSupervises control systems teams, manages process control strategies in manufacturing plantsDesigns, develops, and optimizes manufacturing processes, often in labs or plant settings
Employer & IndustryManufacturing, oil & gas, chemical industriesChemical, pharmaceutical, manufacturing industries

The Process Control Manager oversees the implementation and maintenance of control systems, focusing on team management and strategy. In contrast, the Process Engineer concentrates on designing and improving processes. Both roles require technical expertise but differ in scope and responsibilities.

What are some typical challenges a process control manager might face in a manufacturing environment?

Process Control Managers often encounter challenges such as integrating new technologies with legacy systems, maintaining process consistency across shifts, and troubleshooting unexpected process deviations. They must also ensure compliance with safety and quality standards while coordinating closely with engineering, production, and maintenance teams. Strong problem-solving skills and effective communication are essential for navigating these complexities and driving continuous improvement initiatives.

What is a process control manager?

A Process Control Manager is responsible for overseeing and optimizing the various control systems and processes used in manufacturing or industrial operations. Their role involves ensuring that production processes run smoothly, efficiently, and safely by managing automated systems, monitoring performance, and implementing improvements. They often work closely with engineering, production, and quality assurance teams to identify issues and enhance process reliability. Additionally, they may be involved in training staff, maintaining compliance with regulations, and deploying new technologies to improve process control.

What are the key skills and qualifications needed to thrive as a process control manager?

To thrive as a Process Control Manager, you need a strong background in engineering or process technology, analytical problem-solving abilities, and experience in manufacturing or industrial environments. Familiarity with distributed control systems (DCS), programmable logic controllers (PLCs), process automation software, and often certifications like Six Sigma or PMP are highly valued. Excellent leadership, communication, and decision-making skills help manage teams and coordinate with cross-functional departments effectively. These competencies are vital for ensuring process efficiency, safety, quality, and continuous improvement within complex production operations.
What job categories do people searching Process Control Manager jobs in Charlestown, MA look for? The top searched job categories for Process Control Manager jobs in Charlestown, MA are:
What cities near Charlestown, MA are hiring for Process Control Manager jobs? Cities near Charlestown, MA with the most Process Control Manager job openings:
Process Control Manager jobs near you
Infographic showing various Process Control Manager job openings in Charlestown, MA as of August 2026, with employment types broken down into 72% Full Time, and 28% Part Time. Highlights an 100% In-person job distribution, with an average salary of $109,784 per year, or $52.8 per hour.

Quality Control Manager (External Operations)

Eli Lilly and Company

Boston, MA • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.


Organization Overview:

Verve Therapeutics Inc., a Wholly Owned Subsidiary of Eli Lilly and Company, Verve Therapeutics, a Lilly Research Labs subsidiary, is a clinical-stage genetic medicines company on a mission to solve cardiovascular disease. Founded by leaders in cardiovascular medicine and gene editing, Verve is developing one-time gene editing treatments aimed at turning chronic management into a single-course cure. Its lead programs target PCSK9 and ANGPTL3 to lower LDL-C, the root cause of cardiovascular disease.

Verve is seeking a Manager, Quality ControlExternalOperation,who will report to the Associate Director, External Quality Control and be responsible for assisting with the continued implementation, and management of Quality Control activities at contract manufacturers andcontract testing laboratoriesforLNP and other drugproductcomponentsfor earlydevelopment stages. We are looking for a candidate with strong technical and compliance experience to support a pipeline of gene-editing products.

Responsibilities:

Verve's Quality Control is seeking a candidate for theteamtomanageday-to-day Quality Controloperations at external partners. This individual will be working with theAssociate DirectorofQualityControl and will be supportingin-process, release, and stability testing bycoordinatingwith external partners.The position will be part oftheTechnical Operations team that aims to advance preclinical gene editing candidates into the clinic and works closely withQuality Assurance,External Manufacturing, Process Development, and internal/externalQualityControl.

  • Manage cGMP testing (in-process, release, stability) at CDMOs and contract laboratories.

  • Manage day-to-day Quality Control Operations atexternalpartners.

  • Manage laboratory investigations, deviations, change controls,CAPAsand risk assessments.

  • Manage the review and approval of Quality Control data and CoA/CoTs.

  • Manage material specifications for excipients, drugsubstancesand drug products.

  • Manage the shipment of quality control samples from/to CDMOs and contract laboratories.

  • Assistin coordination, oversight, and review of method validations at CDMOs and contract laboratories.

  • Coordinatestabilitysample storage and testingperapproved protocols.

  • Other duties as assigned

Basic Requirements:

  • B.S. or M.S. degree in chemistry, biochemistry, biological sciences, pharmaceutical sciences, or related field.

  • 5+yearsofrelevantexperience inthe pharmaceutical orbiotechnology industry

  • 3+ years ofdemonstratedquality experience ina cGMP-regulated QC laboratory.

  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Skills/Preferences:

  • Technical experiencewith QC analytical techniques, such as HPLC, GC, CE, UV-VIS, ELISA, andcell-based potency assays.

  • Ability to communicate across various cross-functional teams

  • Experience authoring, reviewing and approving documents inElectronicDocument Management Systems(Veeva).

  • Knowledge and understanding of ICH guidelines, FDA/EMA regulations, and cGMP documentation practices.

  • Experiencewith external vendormanagement(client orclient facing function)

  • Strong self-management and organizational skills, ability to prioritize, critical decision-makingskills, and problemsolving.

  • Self-motivationandleadingthe way for ensuring a fair andequitablework environment

  • Thorough attention to detail, with the ability to critically analyze ideas, data, and reports.

  • Strong oral and written communication and interpersonal skills

Additional Information:

  • Thisis a hybrid position witha mandatory3days a weekon-siteat theFenway location in Boston, MA.

  • Travel Percentage (%): 10%

  • Overtime and shift work may berequiredto support GMP production at external CDMOs.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.


Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).


Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$71,250 - $161,700

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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About Eli Lilly

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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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