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Control M Jobs in Massachusetts (NOW HIRING)

Consigli Construction

M/E/P Estimator

Milford, MA · On-site

$129K - $134K/yr

Chief Estimator, M/E/P Supervisory Duties: Yes Salary Range: $129,000 - $134,000 Estimate the most ... Ensure quality control of bids and estimates. * Prepare an in-house budget and GMP. Key Skills

Consigli Construction

M/E/P Estimator

Milford, MA · On-site

$129K - $134K/yr

Chief Estimator, M/E/P Supervisory Duties: Yes Salary Range: $129,000 - $134,000 Estimate the most ... Ensure quality control of bids and estimates. * Prepare an in-house budget and GMP. Key Skills

Consigli Construction

M/E/P Estimator

Milford, MA · On-site

$129K - $134K/yr

Chief Estimator, M/E/P Supervisory Duties: Yes Salary Range: $129,000 - $134,000 Estimate the most ... Ensure quality control of bids and estimates. * Prepare an in-house budget and GMP. Key Skills

Astrix Inc

Quality Control Inspector II

Shrewsbury, MA · On-site

$35 - $40/hr

M-F 8a-5p Job Summary The Contract Quality Control Inspector II reports to the Quality Inspector Lead, QA Manager, or Director and is responsible for supporting the ISO 9001 Quality Management System.

Man Group plc

Senior Quantitative Developer

Boston, MA · On-site

We use Control-M and Airflow for workflow management, Kafka for data pipelines, Bitbucket for source control, Jenkins for continuous integration, Grafana + Prometheus for metrics collection, ELK for ...

Man Group

Senior Quantitative Developer

Boston, MA · On-site

$150 - $170/hr

We use Control-M and Airflow for workflow management, Kafka for data pipelines, Bitbucket for source control, Jenkins for continuous integration, Grafana + Prometheus for metrics collection, ELK for ...

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All JobsControl M JobsControl M Jobs in Massachusetts

Control M information

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$12

$23

$45

How much do control m jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for control m in Massachusetts is $23.71, according to ZipRecruiter salary data. Most workers in this role earn between $16.78 and $25.48 per hour, depending on experience, location, and employer.

What is a Control M?

A Control-M job is a scheduled task or workflow automated using the Control-M workload automation software. It defines when, where, and how a task should execute, often integrating with various applications, databases, and systems. Control-M jobs help organizations streamline batch processing, improve efficiency, and ensure timely execution of critical tasks.

What does a Control M do?

As a Control M specialist, your daily activities often include designing, scheduling, and monitoring batch jobs using Control-M software to ensure workflows run efficiently. You'll be responsible for troubleshooting job failures, optimizing job schedules, and coordinating with application and infrastructure teams to address issues or deploy changes. Additionally, maintaining documentation, implementing process improvements, and participating in system upgrades or migrations are common duties. The role often requires working both independently and collaboratively to meet operational and project-based goals.

What are the key skills and qualifications needed to thrive in the Control M position, and why are they important?

To thrive as a Control M professional, you need expertise in job scheduling, batch processing, and IT workflow automation, often supported by a degree in computer science or a related field. Familiarity with Control-M software, scripting languages (such as Shell or Python), and ITIL or relevant certifications are highly valued. Strong analytical skills, attention to detail, and effective communication are essential soft skills in this role. These competencies help ensure efficient system operations, minimize downtime, and foster productive collaboration within IT teams.

What are the roles in Control M?

Roles in Control M typically include administrators, who manage and configure the workload automation system; operators, who monitor and execute scheduled jobs; and developers or engineers, who create and maintain job workflows. These roles require knowledge of job scheduling, scripting, and system integration to ensure reliable automation across IT environments.

What are the most commonly searched types of Control M jobs in Massachusetts?

The most popular types of Control M jobs in Massachusetts are:

What are popular job titles related to Control M jobs in Massachusetts?

For Control M jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Control M jobs in Massachusetts look for?

The top searched job categories for Control M jobs in Massachusetts are:

What cities in Massachusetts are hiring for Control M jobs?

Cities in Massachusetts with the most Control M job openings:

Control M jobs near you
Infographic showing various Control M job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 2% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $49,313 per year, or $23.7 per hour.

Director, Quality Control

Editas Medicine

Cambridge, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Job description

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.
Why Choose Editas?
At Editas Medicine, we're a team of courageous problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what's possible in medicine, come join us and become an Editor!
Decoding The Role:
The Quality team is seeking a highly motivated and experienced technical and organizational leader in gRNA, mRNA, and Lipid Nanoparticle (LNP) analytical methodologies and GMP testing. The successful candidate will collaborate with a high-performing CMC team, coordinating with process and analytical experts cross-functionally in Research and Discovery, Process Development, Analytical Sciences, Manufacturing, and Quality Assurance, to transfer, qualify and oversee in-process and release testing to advance Editas' in vivo gene medicine portfolio. The individual will also be a key contributor to the overall program CMC strategy. This role requires strong analytical expertise, GMP experience, as well as a passion to lead, mentor and influence people.
Characterizing Your Impact:
As the Director, Quality Control, you will:
  • Lead phase appropriate CMC analytical development, qualification/validation, transfer and optimization through strong collaboration with key stakeholders and external partners.
  • Drive the analytical control strategy for in vivo medicines towards IND/CTA and clinical manufacturing.
  • Ensure seamless transition of analytics from Analytical Sciences and into GMP manufacturing.
  • Collaborate with QA to generate, review and approve documentation, including: SOPs, change controls, deviations, CAPAs and OOS/OOT investigation reports.
  • Act as the lead Subject Matter Expert for gRNA, mRNA, and drug delivery (e.g., LNP) control strategy to direct the.
  • Establish phase-appropriate specifications based on sound scientific rationale for critical starting materials (e.g. pDNA), drug substance (e.g. gRNA and mRNA), excipients (e.g. lipids and targeting moieties), and drug product (e.g. LNP).
  • Oversee the external GMP testing of critical starting materials, novel excipients, drug substance and drug product for clinical use.
  • Implement stability programs to establish the retest dates/shelf life of critical starting materials, novel excipients, drug substance and drug product for clinical use.
  • Lead cross-functional projects/working teams, champion new ideas/business process improvements to advance company's in vivo pipeline and technology platforms.
  • Author and review of regulatory submissions, technical reports, SOPs and work instructions.
  • Stay up to date with the latest industry trends and product knowledge.
  • Work cross-functionally (e.g. with Research, Business Development and Legal) to evaluate novel manufacturing technologies and new business partners.

Requirements
The Ideal Transcript:
To thrive in this role, you'll need:
  • Degree in Microbiology, Biomedical Engineering, Chemistry, Pharmaceutical Sciences, or related discipline with 8+ (Ph.D.), 10+ (M.S.), 12+ (B.S.) years of relevant experience in drug development.
  • Strong technical expertise and hands-on experience with analytical test method optimization, validation, and transfers as well as CTO/CMO management are required.
  • In-depth expertise in critical raw material, drug substance, and drug product characterization methods and specifications are highly desirable.
  • Ability to develop analytical control strategies that are phase-appropriate (i.e., phase 1 vs. phase 3 requirements) and grounded in principles of risk management.
  • Ability to apply Quality-by-Design (QbD) principles to process development strategy planning and execution is required.
  • Exceptional leadership and interpersonal skills as well as excellent presentation and scientific/technical writing skills is a must.
  • Strong organizational skills, and ability to multi-task, problem-solve, and adjust priorities to meet goals in a fast-paced environment.
  • Experience in leading cross-functional collaborations with other internal departments as well as external CDMOs.
  • Understanding related industry guidance's (FDA, PDA, ICH and BPOG), knowledge of FDA, EMA and ICH regulations, and understanding of product development life cycle.

Benefits
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
Salary Range:
$215,000 - $235,000
Pay Transparency
Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

Apply