Supervisor Environmental Monitoring

Curium Pharma; Maryland Heights (MO); Hybrid; USD 110,000 - 140,000; Full time

Job summary

Curium Pharma is seeking a Supervisor of Environmental Monitoring to lead a multinational QC unit under GMP conditions. You will manage environmental monitoring of controlled environments, ensure timely, accurate data, and drive cross-functional collaboration to meet KPI targets.

Monday–Friday 7am–3:30pm, with emphasis on safety and continuous improvement. The role requires 10+ years in quality/control lab settings, strong cGMP knowledge, and proven supervisory experience, plus expertise in

Qualifications

• Bachelor degree in Chemistry, Science or related field; work experience acceptable in lieu.
• 10+ years of relevant experience with at least 2 years in a supervisory role.
• Strong knowledge of cGMP requirements.
• Strong knowledge of laboratory equipment and product validation.
• Experience with regulatory requirements (FDA, HC, TGA, EU, ISO, USP, etc.).
• Analytical method validation experience.
• Understanding of Quality systems.
• Ability to use software to process and analyze data.

Responsibilities

• Supervise multi-shift laboratories (Environmental Monitoring) ensuring product quality and conformance.
• Maintain operational compliance with US and international regulatory guidelines.
• Ensure all necessary testing is carried out.
• Approve specifications, sampling instructions, test methods, procedures and other QC procedures.
• Approve and monitor any contract testing laboratory for compliance and test results.
• Lead continuous improvement and safety initiatives.
• Maintain ALARA goals and safety procedures.
• Provide leadership for employee relations through coaching and development.

Skills

Supervisory experience

cGMP knowledge

Laboratory validation

Analytical method validation

Quality systems

Data analysis software

Education

Bachelor's degree in Chemistry or related field

Job description

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Maryland Heights, MO, United States, 63043

About Curium

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

The Supervisor of Environmental Monitoring is responsible for ensuring accountability, transparency, and effective communication cross-functionally and within his/her team while ensuring information is timely, clear and accurate. Coaching and developing will foster team ownership that ensures compliance with all policies, procedures and regulations. In addition, must supply the highest level of both internal and external customer service and measure and communicate the team’s progress against individual, team and site goals and Key Performance Indicators (KPI’s).

The Supervisor of Environmental Monitoring manages the activities of a pharmaceutical quality control unit in the performance and analysis under GMP conditions for the entire site. Scope of responsibility includes environmental monitoring of controlled environments to assure controlled environments are maintained.

Schedule: Monday – Friday 7am – 3:30pm

Essential Functions

• Supervise multi-shift laboratories (Environmental Monitoring) ensuring that performance and quality of products conform to establish standards and regulatory requirements.
• 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 all necessary testing is carried out.
• Approve specifications, sampling instructions, test methods, procedures and other QC procedures.
• Approve and monitor any contract testing laboratory for compliance and test results.
• Ensure appropriate validations/qualifications are completed and approved.
• Ensure laboratory records are evaluated and signed by an authorized person before they are sent to the QA department.
• Ensure accountability, transparency, and effective communication cross-functionally and within the team while guaranteeing information is timely, clear and accurate.
• Coach and develop the team to team ownership.
• Ensure team compliance with all policies, procedures and site/company regulations.
• Set clear vision by ensuring goals and objectives are aligned with site strategies and managing each team member’s performance management.
• Exhibit accountability and responsibility for an area or process in order to affect change and lead efforts and ideas to completion.
• Provide leadership for employee relations through effective communications, coaching, training and development and eliminate roadblocks in order for the team to move forward.
• Supply the highest level of internal and external customer service while having the ability to diplomatically challenge established procedures and systems.
• Understand and provide education and feedback to team regarding business and financial impact of decisions/actions.
• Ensure all direct reports maintain ALARA and manage their daily activities accordingly to ensure they meet their quarterly ALARA goals.
• Ensure strong adherence to safety procedures.
• Ensure team meetings are held to update team and track progress.
• Lead team in continuous improvement activities.
• Ensure proper maintenance and cleanliness of the department, premises and equipment.
• Measure and communicate team’s progress against individual, team and site goals and Key Performance Indicators (KPI’s).
• Maintain an acceptable level of 5S in the area. Assure the laboratories are maintained to promote an organized workspace.
• Recognize and reward performance.
• Lead and/or support all investigations. Review and approve area quality and safety exceptions and investigation reports. Ensure on-time completion of investigations and corrective action items assigned to area.
• Verify, review and make appropriate changes if needed, to any controlled document pertinent to area of responsibility.
• Identify opportunities to reduce risk, reduce cost of poor quality and improve service.

Requirements

• Bachelor Degree in Chemistry, Science or related field is required. Work experience is considered in lieu of degree.
• 10 or more years of relevant experience required with two years of supervisory experience required.
• Strong knowledge of cGMP requirements.
• Strong knowledge of laboratory equipment/product validation.
• Complete understanding and application of principles, concepts, practices, and standards for testing performed in all QC laboratories through hands‑on experience working in a Pharmaceutical manufacturing facility laboratory.
• Expertise in the manufacture and control of finished products, analytical analysis techniques and statistical quality control.
• Working knowledge of regulatory (FDA, HC, TGA, EU, ISO, USP, etc.) requirements and applicable testing Guidelines.
• Background must include analytical method validation work.
• Thorough understanding of Quality systems.
• Ability to use relevant software packages to process and analyze data.

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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