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Control M Jobs in Wisconsin (NOW HIRING)

Soteria Reinsurance Ltd.

$44.75 - $57.75/hr

SQL Knowledge in Assembler, REXX, JCL, JAVA, Control-M a plus but not required. The Skills You Bring You have experience and feel confident working in an agile environment (Scrum and Kanban)

Essel

Collect and verify O&M manuals, training materials, warranties, and attic stock for turnover to ... Relevant certifications in QA/QC practices are a plus. * Valid driver's license and reliable ...

New

State of Wisconsin

System Administrator

Madison, WI · On-site

$41.03 - $57/hr

Press Control+M to start dragging object All employees are expected to live and work in Wisconsin. This position will have the option of working remotely upon agreement of the supervisor but may be ...

Qualysoft

Expert:in Testautomatisierung (f/m/d) Location: Wien (1-2 Tage/Woche vor Ort), ansonsten Remote Start: Q1 2026 | Duration: 12 Monate | Workload: 100% Languages: German 360 - 400 a day Ihre Aufgaben ...

State of Wisconsin

Legal Associate

Madison, WI · On-site

$29.28/hr

Press Control+M to start dragging object Provide administrative and legal support as a Legal Associate for the Division of Hearings and Appeals, Corrections Unit. This position is headquartered at ...

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$11

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How much do control m jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for control m in Wisconsin is $21.91, according to ZipRecruiter salary data. Most workers in this role earn between $15.53 and $23.56 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 popular job titles related to Control M jobs in Wisconsin?

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

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

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

Control M jobs near you
Infographic showing various Control M job openings in Wisconsin as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $45,576 per year, or $21.9 per hour.

Scientist II, Quality Control

Verona, WI • On-site

Arrowhead Pharmaceuticals
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Arrowhead Pharmaceuticalsexternal

$105K - $120K/yr

Full-time

Re-posted 6 days ago

Key responsibilities

  • Support analytical method validation, transfer, and testing of pharmaceutical raw materials, in-process samples, finished drug substances, drug products, and stability samples.

  • Lead and coordinate analytical projects, including technical discussions, data analysis, and preparation of reports and SOPs.

  • Perform testing using various analytical techniques such as LCMS, HPLC/UPHPLC, GC, FTIR, UV/Vis, and KF, and interpret experimental results.

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
This position is within the Quality Control structure, under the Quality Organization. Scientist II, Quality Control, will support the analytical method validation, method transfer and testing of pharmaceutical raw materials, in process manufacturing samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. Scientist II is expected to be proficient in several analytical techniques and will be capable of making independent scientific decisions. The position also requires the ability to lead and mentor co-workers. This position reports to QC Laboratory Management.
Responsibilities
  • Know and adhere to Arrowhead Core Values, cGMP policies and procedures and relevant SOPs
  • Work independently and with Analytical Development and manufacturing team to lead project timelines and deliverables.
  • Owns and leads scientific technical discussions and brainstorming sessions with internal and external stakeholders.
  • Guide junior scientists with technical guidance and training
  • Serve as Analytical Project Coordinator or coordinate for on-going or new Analytical Validation and technical transfer projects, take ownership of analytical requirements needed, and provide accurate analytical results
  • Prepare Analytical Validation technical reports, presentations, SOPs, and policies and procedures
  • Support analytical methods optimization and improvement of existing ones, to support all stages of API (active pharmaceutical ingredient) and drug product.
  • Ability to track/trend data and interpret degrative changes to the product on
  • Demonstrate proficiency with various related analytical techniques, such as LCMS, HPLC/UPHPLC, GC, FTIR, UV/Vis, KF.
  • Design and execute non-routine experiments.
  • Analyze data/results and interpret outcome of experiments and propose appropriate follow-up
  • Write project documentation (i.e. Analytical test methods, developmental reports and protocols)
  • Assist with drafting Out of Specification and Deviations with minimal supervision
  • Perform testing of test samples in support of API and drug release.
  • Performs technical data review on data acquired by other QC analysts as applicable
  • Other duties as assigned

Requirements
  • M.S. in Chemistry (or related field) with at least 8+ years of relevant laboratory experience, or B.S in Chemistry (or related field) with at least 12 years of laboratory experience.
  • Experience and working knowledge of various related analytical techniques, such as LCMS, HPLC/UHPLC, GC, FTIR, UV/Vis, LC/MS, KF, etc.
  • Familiar with analytical instrumentation, test methodology/validations, data acquisition systems, and cGMP policies and practices
  • Skills and knowledge in handling, analyzing and characterizing chemicals, pharmaceuticals and related organic molecules
  • Knowledgeable of cGMP, ICH, CDER requirements
  • Understanding of basic theories and principles of synthetic organic chemistry
  • Strong attention to detail.
  • Can perform tasks assigned with minimal supervision
  • Works well with others and in a team environment
  • Can be flexible with changing priorities

Wisconsin pay range
$105,000-$120,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
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