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TILE DISTRIBUTION - MATERIAL HANDLER II (2ND SHIFT)
Helsinki, Uusimaa, Finland · On-site
Mid level$600M raised
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TILE DISTRIBUTION - MATERIAL HANDLER II (1ST SHIFT)
Helsinki, Uusimaa, Finland · On-site
Mid level$600M raised
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Full-time
high school, associate degree
Posted 3d ago
Apply by Jun 13
~40 hrs/week
Responsibilities
Perform aseptic preparation, formulation, and dispensing of radiopharmaceutical products within an ISO 5 cleanroom. Ensure strict adherence to cGMP guidelines, safety protocols, and FDA regulations while maintaining production equipment.
Requirements
Requires a high school diploma or equivalent, with an associate degree preferred and at least three years of relevant manufacturing experience in a regulated environment. Must be able to work rotating shifts and perform physically demanding tasks, including lifting up to 70 pounds.
Full job description
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
Performs all tasks associated with preparing, formulating and dispensing aseptically manufactured products in and ISO 5 cleanroom environment according to cGMP Guidelines in order to meet production demands.
Schedule: Monday through Thursday 0500-1530. Weekend and off shift overtime as needed.
Essential Functions
Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines, SOP’s and FDA regulations.
Responsible for following detailed instructions and communicating effectively, both written and verbally.
Perform Batch Record calculations and maintain all documentation according to cGMP Guidelines.
Set up, maintain, and clean appropriate equipment and work area according to SOP and in compliance with cGMP guidelines.
Set up, operate, and monitor production equipment and processes in accordance with current good manufacturing practices and standard operating procedures.
Calibrate or adjust equipment to ensure quality production, using internal calibration functions.
Participate and perform effectively in a team environment and interact with multiple departments to ensure the operational success of the team.
Adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance.
Troubleshoot problems with equipment, devices, or products.
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.).
Requirements
Associate Degree preferred, High school diploma or equivalent required.
Three or more years of relevant manufacturing experience required (regulated environment, attention to detail and following detailed instruction).
Knowledge of Good Manufacturing Practices c(GMP) and applicable Quality System Standards.
Willingness to work rotating shifts, weekends, and overtime, as necessary.
Effectively adjusts to changes and deals effectively with uncertainties in the workplace.
Ability to generate new and valuable ideas and effective solutions to difficult problems; connects previously unrelated notions.
Realizing the worth of all people and respects others, regardless of background or cultural differences.
Thoroughly understanding the needs of internal/external customers and making customer satisfaction a top priority.
Strong motivation and ability to achieve work goals and quantifiable business results.
Ability and desire to cooperate, collaborate, and partner with others.
Willingness to help outside your department and within your department outside your normal or assigned responsibilities.
Has demonstrated the use of logical methods to solve problems with effective solutions and able to make quick quality decisions.
Dedicated to providing the highest quality product and meeting the expectations and requirements of internal and external customers.
Takes ownership and accountability for the production process, assigned production area, production equipment and associated documentation.
Good interpersonal skills and ability to communicate information in a timely manner to those who need the information.
Drive self and team to schedule adherence and most efficient production process.
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 an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Driving innovation in nuclear medicine to improve patients’ lives
Industry
Pharmaceutical Manufacturing
Company size
1,001-5,000 employees
Founded
2017
Headquarters
Boston, Massachusetts
LinkedIn followers
79,058
Curium is the global leader in nuclear medicine, providing life-changing diagnostics and treatment to patients all over the world.
We develop, manufacture and distribute world-class radiopharmaceutical products with a renewed focus on cancer, exploring untapped potential for new innovation.
We build on remarkable foundations and a legacy of providing reliable and consistent nuclear solutions to tens of thousands of patients every day. Our proven heritage combined with a pioneering approach are the hallmarks from which we provide life-changing diagnostics and therapeutics. Our people are the root of the incredible impact they have.
As part of our 2030 vision to become an oncology-focused nuclear medicine leader – both in diagnostics and therapy – we will expand our reach further into Japan and China, continuing to roll out our superior products to a global market. The impact of these investments on patients will be life changing.
Our cancer focus is currently in Neuroendocrine Tumors (NETs) and prostate cancer PSMA. We are also working on leveraging the power of AI to improve image quality and accuracy; to identify patterns to help diagnose pathologies and of course to better support physicians.
Our Promise
We strive to make the impossible possible and to be an organization that will change the face of medicine. Our diverse group of industry experts is unified under one strong and singular focus – to develop, manufacture and supply revolutionary diagnostic and therapeutic radiopharmaceuticals to our customers around the globe with unrivaled reliability and superior service.
Offices: 2 Seaport Ln, 2nd floor, Boston, Massachusetts 02210, US · 20, rue Quentin Bauchart, Paris, France 75008, FR · 111 Westport Plaza, Suite 800, St. Louis, MO 63043, US · Biopôle Clermont-Limagne 3 rue Marie Curie 63360, Saint-Beauzire, FR · Westerduinweg 3, Petten, North Holland 1755, NL
Nuclear MedicinePET ImagingMolecular ImagingcGMP Manufacturing Contract Manufacturingand SPECT ImagingWholesalePharmaceuticalCustomer Service
How many Manufacturing jobs are open in Helsinki, Finland right now?
There are currently 1,046 open manufacturing positions in Helsinki, Finland listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Helsinki, Finland?
Companies currently hiring include Mohawk Industries, Rollon Americas, Chart Industries, Inc., Armstrong World Industries, Fives, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Helsinki, Finland?
Yes — 50 of the 1046 open manufacturing positions offer remote or hybrid work (11 remote, 39 hybrid).
How do I apply for Manufacturing jobs in Helsinki, Finland?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.