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(Contractor) Technical Writer
Curium Pharma Maryland, MO
$85k-103k (estimate)
Contractor | Wholesale 2 Weeks Ago
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Curium Pharma is Hiring a (Contractor) Technical Writer Near Maryland, MO

(Contractor) Technical Writer
Date: Apr 30, 2024
Location:

Maryland Heights, MO, United States

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 R&D Technical Writer position will report to the Senior Director of Downstream R&D. The successful candidate will serve as a technical team member and will support the drafting technical documents and development reports consistent with the project schedule.

Essential Functions
  • Prepares written project documents, including reports, memoranda, and SOPs.
  • Author and create submission content from source documentation for registrations and provide writing support for technical reports.
  • Use experience in Process Development to identify technical inconsistencies and participate in resolution.
  • Strong written and oral communication skills to summarize studies from reports, presentations, and notebooks and a demonstrated ability to document information in a clear and concise manner.
Requirements
  • Bachelor degree in chemistry, Chemical Engineering, Biochemistry, Biology, Life Sciences, or related field required.
  • 3 or more years of relevant experience required.
  • Demonstrated knowledge of pharmaceutical manufacturing and process development
  • Knowledge of product lifecycle - Product and process development, validation, regulatory submissions, and commercial GMP manufacturing.
  • Demonstrated experience working with Microsoft Office programs (Excel, Word, Power Point, Visio, etc.).
  • Behavioral requirements for success in this position include self-starter, strong work ethic, excellent written and verbal communication skills.

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.

Job Segment: Technical Writer, Biochemistry, Medical Technologist, Nuclear Engineering, Chemical Engineer, Technology, Science, Healthcare, Engineering

Job Summary

JOB TYPE

Contractor

INDUSTRY

Wholesale

SALARY

$85k-103k (estimate)

POST DATE

05/02/2024

EXPIRATION DATE

07/01/2024

WEBSITE

curiumpharma.com

HEADQUARTERS

SAINT LOUIS, MO

SIZE

1,000 - 3,000

FOUNDED

2017

CEO

RENAUD DEHARENG

REVENUE

$50M - $200M

INDUSTRY

Wholesale

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About Curium Pharma

About Curium Curium is the worlds 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. Our Single Focus Our diverse group of industry experts is unified under one strong and singular focus to develop, manufacture and supply SPECT, PET and therapeutic radiopharmaceuticals to customers around the globe. Our Global Reach W ... e service millions of patients worldwide using sizable global logistics and experience. By utilizing our combined resources, we can deliver superior solutions to 6,000 customers in 70 countries. Our Product Portfolio We have one of the largest vertically integrated radiopharmaceutical manufacturing networks in the industry. This includes: 1 Molybdenum facility, 3 large SPECT facilities and close to 40 PET & SPECT radiopharmacies across the United States and Europe. The products we supply are best-in-class and we are committed to developing and launching more in the years to come. Superior Reliability and Quality We strive to build and foster long-term partnerships with our customers through exceptional service reliability and dedication to our industry. Our goal is to be a trusted partnerone that contributes to the future business growth and sustainability of our customers Our Values Our core valuesintegrity, commitment and collaborationdrive every aspect of our behavior. It is our dedication to these values that truly sets us apart from the competition. Life Forward This is much more than our brand tagline. It is a commitment to our customers and those we serve by enhancing the quality of health outcomes through patient care. It is a demonstration of years spent striving for excellence, world-class service and a vision for growth. More
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If you are interested in becoming a Technical Writer, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Technical Writer for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

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Take advantage of the writer's knowledge of publishing.

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Pursue a technical writer certification.

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Understand the topic carefully.

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Simplification of any terms whenever needed.

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Step 3: View the best colleges and universities for Technical Writer.

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