Environmental Monitoring Technician

Curium Pharma; Maryland Heights (MO); On-site; USD 35,000 - 55,000; Full time

Job summary

A leading company in nuclear medicine is seeking an Environmental Monitor to oversee the safety and quality of pharmaceutical manufacturing environments. This position includes working with diverse teams, ensuring compliance with safety protocols, and engaging in various monitoring activities. Ideal candidates will possess an associate degree in life sciences or equivalent coursework, coupled with strong analytical and interpersonal skills.

Qualifications

• Associate degree or relevant life sciences coursework required.
• Good writing and verbal communications skills.
• Familiarity with laboratory monitoring equipment.

Responsibilities

• Perform routine environmental monitoring of aseptic processing areas.
• Ensure compliance with regulatory guidelines and SOPs.
• Conduct various testing and monitoring activities.

Skills

Analytical skills

Problem-solving

Decision-making skills

Interpersonal skills

Communication skills

Teamwork

Education

Associate degree in life sciences

Completion of college-level life science courses

Job description

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Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service.

With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.

Summary of Position

Perform routine environmental monitoring of aseptic processing and controlled area cleanroom environments used for pharmaceutical manufacturing. Perform assigned quality control or quality assurance activities in compliance with applicable SOP's and cGMPs.

Schedule:
Combination of 1st and 2nd shift, 5-week rotating schedule repeating the following schedule:
Week 1: Mon-Th 0600-1430
Week 2: Sat 1700-2100, Sun-Wed 1200-2130
Week 3: Sun 0400-1230, Mon-Thur 0500-1330
Weeks 4-5: Mon-Fri 0700-1530

Essential Functions

• Ensure a safe and quality working environment through training, awareness, and compliance with Safety/Quality guidelines and SOP’s.
• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
• Ensure the maintenance of the department, premises, and equipment.
• Ensure that all necessary testing is carried out by required due dates. Perform all assigned tasks confidently and consistently.
• Perform monitoring using lab equipment and techniques (SAS, SMA, Met One particle counter, viable airborne monitoring (active and passive), total airborne particulate sampling, viable surface monitoring, personnel monitoring, and membrane filtration of water samples). Ensure assigned tasks are performed confidently and consistently.
• Ensure the use of proper aseptic technique during testing of controlled environments and utility systems.
• Perform all work in compliance with site quality, site safety and radiation protection guidelines. Collaborate with team members to ensure quality tasks is performed in a timely manner.
• Must demonstrate flexibility in adjusting to changing priorities and schedules.
• Attend mandatory training as required by site regulatory requirements and management. Assist with investigations.
• Perform other general duties associated with the position as required by supervision.

Requirements

• Associate degree or completion of college-level life science courses required. Work experience is considered in lieu of degree.
• Good interpersonal, hands on, analytical, problem solving and decision-making skills.
• Excellent writing and verbal communications skills.
• Good computer skills, including utilizing personal computers and data entry programs.
• Ability to work independently and with others to accomplish goals and priorities.
• Flexibility and teamwork skills, high level of energy and regular, consistent attendance.

Working Conditions:

• Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
• Responsibilities include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment.
• Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury.
• Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed.
• May be required to sit or stand for long periods of 8+ hours a day while performing duties.
• Must possess good hand-eye coordination; close attention to detail is required.
• Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants.
• Willingness to complete safety training within allotted timeframes, and work in a team-based environment.
• Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.
  

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

Equal Opportunity Employer

Curium is anequal opportunity employerand believes everyone deserves respect, dignity and equality. All applicants will be considered for employmentwithout attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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