Experience leading medical, or other regulated industry, product development. * Experience in ... Excellent requirements and specification writing skills. * Demonstrated deep understanding of US ...
60 Katalyst Medical Writer Jobs Hiring Near You
Experience leading medical, or other regulated industry, product development. * Experience in ... Excellent requirements and specification writing skills. * Demonstrated deep understanding of US ...
Medical Device Quality Engineer
$75.20K - $97.20K/yr
Summary : Seeking an experienced Medical Device Quality Engineer to support the launch of a new ... Write and maintain SOPs, work instructions, and process documentation to support repeatable, high ...
Medical Device Quality Engineer
$75.20K - $97.20K/yr
Summary : Seeking an experienced Medical Device Quality Engineer to support the launch of a new ... Write and maintain SOPs, work instructions, and process documentation to support repeatable, high ...
Strong capability in test protocol report writing, statistical analysis (9595, tolerance intervals ... medical device industry
Strong capability in test protocol report writing, statistical analysis (9595, tolerance intervals ... medical device industry
... medical devices from concept through commercialization, or across the full product life cycle ... Strong technical writing and communication skills.
... medical devices from concept through commercialization, or across the full product life cycle ... Strong technical writing and communication skills.
Excellent technical writing skills. * Prior experience initiating/writing, evaluating and completing Corrective and Preventive Actions (CAPA). * Work experience in a medical device/ pharmaceutical ...
Excellent technical writing skills. * Prior experience initiating/writing, evaluating and completing Corrective and Preventive Actions (CAPA). * Work experience in a medical device/ pharmaceutical ...
Roles & Requirements: * 5+ Years' experience in medical device V&V for a large company. * Experience with FDA-regulated V&V. * IEC 62304 experience. * Meaningful direct experience in writing ...
Roles & Requirements: * 5+ Years' experience in medical device V&V for a large company. * Experience with FDA-regulated V&V. * IEC 62304 experience. * Meaningful direct experience in writing ...
Associate QC Chemist II
$24.25 - $32/hr
Writes procedures with guidance. Works under the guidance of a supervisor but can manage time ... BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree. * 3 + ...
Associate QC Chemist II
$24.25 - $32/hr
Writes procedures with guidance. Works under the guidance of a supervisor but can manage time ... BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree. * 3 + ...
Medical Device or Pharmaceutical Experience Required. Preferred Medical Device with 3-5 Years ... Excellent oral and written communication skills.
Medical Device or Pharmaceutical Experience Required. Preferred Medical Device with 3-5 Years ... Excellent oral and written communication skills.
Ability to effectively communicate across multiple audiences, including operators, peers and management, in both written and oral manners * Process validation experience. * Experience in a Medical ...
Ability to effectively communicate across multiple audiences, including operators, peers and management, in both written and oral manners * Process validation experience. * Experience in a Medical ...
Ability to effectively communicate across multiple audiences, including operators, peers and management, in both written and oral manners. * Process validation experience. * Experience in a Medical ...
Ability to effectively communicate across multiple audiences, including operators, peers and management, in both written and oral manners. * Process validation experience. * Experience in a Medical ...
Experience in medical device manufacturing is required. * Experience in process validation planning, execution and reporting is required. * Strong technical writing skills related to process ...
Experience in medical device manufacturing is required. * Experience in process validation planning, execution and reporting is required. * Strong technical writing skills related to process ...
Experience in the Medical Device Industries with experience in the Manufacturing Process Validation. * Demonstrates excellent written and verbal communication skills (English and Spanish) across all ...
Experience in the Medical Device Industries with experience in the Manufacturing Process Validation. * Demonstrates excellent written and verbal communication skills (English and Spanish) across all ...
Quality Engineer
$80.70K - $104.20K/yr
Medical Device Quality Engineer responsible for supporting the launch of a new medical device ... Write, maintain, and control SOPs, work instructions, and process documentation to support ...
Quality Engineer
$80.70K - $104.20K/yr
Medical Device Quality Engineer responsible for supporting the launch of a new medical device ... Write, maintain, and control SOPs, work instructions, and process documentation to support ...
We are seeking an experienced Project Manager with a strong background in medical device component ... Excellent communication skills; must be highly proficient in reading, writing, and speaking English.
We are seeking an experienced Project Manager with a strong background in medical device component ... Excellent communication skills; must be highly proficient in reading, writing, and speaking English.
Effective verbal and written skills. * Medical terminology knowledge preferred. * Prior experience in a regulatory/medical setting preferred. * Candidates must posses 3 to 5 years of experience or ...
Effective verbal and written skills. * Medical terminology knowledge preferred. * Prior experience in a regulatory/medical setting preferred. * Candidates must posses 3 to 5 years of experience or ...
Manufacturing Process Engineer
$68.70K - $91.60K/yr
Manufacturing Process Engineer with experience in medical device manufacturing, responsible for ... Strong verbal and written communication skills with the ability to effectively communicate at ...
Manufacturing Process Engineer
$68.70K - $91.60K/yr
Manufacturing Process Engineer with experience in medical device manufacturing, responsible for ... Strong verbal and written communication skills with the ability to effectively communicate at ...
... medical device manufacturing. * Strong knowledge of Quality Management Systems, regulatory standards, and industry best practices. * Demonstrated experience writing and managing Quality System ...
... medical device manufacturing. * Strong knowledge of Quality Management Systems, regulatory standards, and industry best practices. * Demonstrated experience writing and managing Quality System ...
Software Controls Engineer
$47.25 - $60.25/hr
... field (medical device is ideal but not required). * Must be mechanically/electrically inclined and okay with extensive field work/dirty hands. * Ideally someone who can also write PLC code and can ...
Software Controls Engineer
$47.25 - $60.25/hr
... field (medical device is ideal but not required). * Must be mechanically/electrically inclined and okay with extensive field work/dirty hands. * Ideally someone who can also write PLC code and can ...
manufacturing Engineer
Blue Ash, OH · On-site
$70.10K - $90.30K/yr
... written and oral manners · Process validation experience. · Experience in a Medical Device and/or regulated manufacturing work environment. · Persuasive communication and interpersonal skills. · ...
New
manufacturing Engineer
Blue Ash, OH · On-site
$70.10K - $90.30K/yr
... written and oral manners · Process validation experience. · Experience in a Medical Device and/or regulated manufacturing work environment. · Persuasive communication and interpersonal skills. · ...
New
Effective verbal and written skills. * Medical terminology knowledge preferred. * Prior experience in a regulatory/medical setting preferred.
Effective verbal and written skills. * Medical terminology knowledge preferred. * Prior experience in a regulatory/medical setting preferred.
Katalyst Jobs Information
What are the key skills and qualifications needed to thrive as a Medical Writer, and why are they important?
To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.
How does a Medical Writer typically collaborate with subject matter experts during a project?
Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.
What are medical writers?
Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.
What is the difference between Medical Writer vs Clinical Writer?
| Aspect | Medical Writer | Clinical Writer |
|---|---|---|
| Credentials | Typically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are common | Similar credentials; often holds degrees in life sciences with certifications in clinical research or writing |
| Work Environment | Works in pharmaceutical, biotech, or healthcare companies, often in offices or remote settings | Primarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings |
| Industry Usage | Used across pharma, biotech, medical device industries for regulatory, educational, and promotional content | Focused on clinical trial documentation, protocols, and reports within clinical research |
Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.
What is it like to work at Katalyst?
Katalyst appears to be a collaborative and innovative company that values creativity and teamwork, fostering an environment where employees can share ideas and work together to achieve common goals.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
What other companies are hiring for Medical Writer jobs?
What are the most popular jobs at Katalyst?
What are the most popular categories at Katalyst?
Job description
Job Summary:
- Overall technical leadership and responsibility for realization of a new product release and sustaining activity.
- Translation of user requirements, requirements management, top-level design, feasibility of potential solutions, decomposition of derived requirements.
- Systems design/architecture and Integration oversight.
- Support for NPI efforts that create value for Clinical Applications and Devices Organization through innovation and design, while delivering high quality engineering solutions.
- Technical liaison to the program.
- Defect/Risk management and Design Reviews.
- BS degree in engineering.
- Experience leading medical, or other regulated industry, product development.
- Experience in leading groups to solutions for complex problems.
- Experience with deriving and simulating human interactions with devices and device use conditions.
- Experience with electronic requirement data management SW – preferably DOORS.
- Minimum five years engineering / R&D experience in a rigorous quality-focused environment.
- Minimum three years' experience in a Systems Engineering role, or a role having overall systems responsibility involving electrical (analog and digital), mechanical, firmware and software development disciplines.
- Excellent requirements and specification writing skills.
- Demonstrated deep understanding of US and international regulatory requirements for a heavily regulated product.
- Ability to build and maintain effective cross-functional and cross-organizational relationships.
- Excellent oral, written and presentation skills.
- In depth knowledge performing risk management per ISO 14971.
- In depth knowledge in developing and testing products to IEC60601-1 Safety standard.
- In depth knowledge in developing and testing products to IEC62336 EMC standard.
- Understanding of US and international regulatory requirements for medical devices strongly preferred.
- Experience developing reliability plans.
- Knowledge of product development processes and best practices.
- Knowledge of verification and validation testing processes.
- Electrical or Software development experience is a plus.
- Master's degree preferred.