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Compound Management Jobs in Connecticut (NOW HIRING)

Marmon

CV Operator | Fri-Sun 7pm-7am

Seymour, CT · On-site

$23 - $27/hr

Load and unload compound boxes/crates on to compound stands. Ensure the correct material strips is ... Submit reports as required by management. Troubleshooting: Quickly and effectively troubleshoot any ...

Polymer Resources, Ltd.

Be Seen First

Color Lab Supervisor (2nd & 3rd Shifts)

Farmington, CT · On-site

$55K - $80K/yr

At Polymer Resources, we compound Engineering Thermoplastic materials that are used in both ... the Lab Manager. In this role the incumbent will assist with organizing mixing operators for ...

System One

Regulatory Affairs Specialist

Trumbull, CT · On-site

$30 - $35/hr

... Compound (VOC) regulations (US), California Prop 65 (US), Federal Insecticide, Fungicide and ... Manage workload, priority and performance of regulatory staff, in addition to providing development ...

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All JobsCompound Management JobsCompound Management Jobs in Connecticut

Compound Management information

See Connecticut salary details

$12

$21

$32

How much do compound management jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for compound management in Connecticut is $21.43, according to ZipRecruiter salary data. Most workers in this role earn between $17.36 and $23.08 per hour, depending on experience, location, and employer.

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

To thrive in Compound Management, you need a solid background in laboratory sciences, attention to detail, and experience handling chemical compounds, often backed by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), inventory tracking software, and best practices for safe handling and storage of substances is highly beneficial. Strong organizational, problem-solving, and communication skills are essential for managing inventory, coordinating with research teams, and addressing logistical challenges. These skills are critical to ensuring compound integrity, supporting scientific workflows, and maintaining safety and efficiency in research environments.

What are the typical daily responsibilities for someone working in Compound Management?

Professionals in Compound Management are responsible for receiving, cataloging, storing, and distributing chemical or biological samples within research or pharmaceutical environments. On a daily basis, you may prepare compounds for experiments, manage inventory records, conduct quality checks, and coordinate with scientists to fulfill project requests. Ensuring proper documentation, compliance with safety standards, and maintaining the integrity of compounds are central to the role. Working closely with researchers and laboratory staff is common, making teamwork and timely communication essential for success.

What is a Compound Management job?

A Compound Management job involves overseeing the storage, tracking, and distribution of chemical compounds in a laboratory or research setting. Professionals in this role ensure that samples are properly organized, labeled, and made available for researchers while maintaining database accuracy and compliance with safety regulations. They may also be responsible for inventory management, automation, and quality control to support drug discovery and development.

What are popular job titles related to Compound Management jobs in Connecticut? For Compound Management jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Compound Management jobs in Connecticut look for? The top searched job categories for Compound Management jobs in Connecticut are:
Compound Management jobs near you
Infographic showing various Compound Management job openings in Connecticut as of July 2026, with employment types broken down into 21% Locum Tenens, 70% Full Time, 4% Part Time, 2% Contract, 1% Nights, and 2% Summer. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $44,581 per year, or $21.4 per hour.
Supervisor, Manufacturing (2nd Shift 2:00pm - 10:30pm, Mon-Fri)

Supervisor, Manufacturing (2nd Shift 2:00pm - 10:30pm, Mon-Fri)

MannKind Corporation

Danbury, CT • On-site

$40.40 - $60.60/hr

Other

PTO

Posted 26 days ago

Job description

At MannKind, our employees are our number one asset, and we foster a tight-knit community where each of us plays a critical role in our collective success. We strive to provide a work environment where diversity of background, thought and perspective is valued and respected. Our team is also energized by the company's entrepreneurial spirit that provides an environment in which you can evolve ideas quickly and nimbly.
Our Values serve as the foundation of MannKind's culture. They define who we are, how we act, and guide our interactions every day-both with each other and the customers we serve. At MannKind, you will work with people who are experts in their fields, see challenges as opportunities, are tenacious and push boundaries, bring creative and solutions-based thinking forward, and always believe in winning together.
Position Summary:
Supervises downstream related activities and staff responsible for cGMP drug product manufacturing. These responsibilities include but are not limited to the supervision of bulk and fill/pack manufacturing shifts, scale-up of processes, innovating novel approaches to improve production efficiency, scheduling of development activities at the commercial scale, supervision of cGMP operations, troubleshooting production challenges, hands on operations during commercial manufacturing batches, and assessing product performance. Executes against and authors, reviews, and approves various cGMP documents such as standard operating procedures, batch records, deviations, process descriptions, validation protocols, and development protocols / reports as required. Collaborates with Quality Assurance, Quality Control, Manufacturing Technical Services, Facilities Engineering, Formulation Research, Process Technology and Validations. Work Schedule is 2nd shift: 2:00pm to 10:30pm, Monday through Friday. 10% Shift Differential.
Essential duties and key job responsibilities and essential functions:
  • Supervise the manufacturing floor/line operations of bulk and semi-finished drug product
  • Supervise / Coordinate Commercial Manufacturing support groups
  • Supervise departmental activities in order to maintain Commercial Manufacturing Clean Room and Potent Compound Facility Areas including participation and overseeing manufacturing operations
  • Supervise off-shifts, PTOs and vacations coverage
  • Train new manufacturing associates on bulk and fill/pack manufacturing processes
  • Author and revise Standard Operating Procedures
  • Author and revise Master Batch records
  • Investigate and complete manufacturing deviations
  • Cover work shifts of other manufacturing supervisors on vacation or PTO, as necessary.
  • Ensure that manufacturing is conducted according to domestic and foreign regulatory agency requirements and MannKind procedures
  • Coordinate the development activities of existing and new product platforms without significant impact to production schedule
  • Short term planning of bulk and fill/pack manufacturing activities to support master production schedule
  • Responsible for observing all Company, Health, Safety and Environmental guidelines.

Duties and responsibilities are not limited to the work listed above and may include other assignments
Minimum qualifications to perform the job; specific skills, education, knowledge and job experience necessary to perform essential duties; physical requirements for job if any.
  • High school diploma with 10+ years related manufacturing / supervisory experience or AA degree with 8 years or BS degree with 8 years or BS degree with 4 years
  • High level of knowledge with process technologies, equipment, and manufacturing of pharmaceutical drug products.
  • Strong knowledge of pharmaceutical quality standards.
  • Experience writing and implementing SOPs in a GMP environment.
  • Must be willing and able to receive medical clearance to wear a respirator (i.e., Powered Air Purifying Respirator) for entire working shift.
  • Must be physically able to gown and de-gown (including the use of a decontamination fogging shower) in up to three layers of clean room and potent compound facility gowning (i.e., Tyvek® jumpsuit).

Pay Range: $40.40 - $60.60 per hour

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