Labeling Specialist

Pay is $36 - $42 per hour based on experience. 24- month assignment with the potential to convert based on performance and headcount approval. Responsible for the design and modification of artwork related to the medical field and provide technical documentation that conforms to company standards and Global Drafting Manual requirements.Design artwork for...

Job DescriptionJob DescriptionAs a Label Compliance Specialist at Amare Global, you will play a crucial role in ensuring that all product labels comply with regulatory requirements set forth by relevant authorities such as the FDA (Food and Drug Administration) and other regulatory bodies. Your attention to detail, and ability to collaborate...

Job DescriptionJob Description***Please note that this is HYBRID role where the ideal candidate will be required to work in our Lehi, UT office 1-2 days per week.***As a Label Compliance Specialist at Amare Global, you will play a crucial role in ensuring that all product labels comply with regulatory requirements set forth by relevant authorities such as...

Please note that this is HYBRID role where the ideal candidate will be required to work in our Lehi, UT office 1-2 days per week. As a Label Compliance Specialist at Amare Global, you will play a crucial role in ensuring that all product labels comply with regulatory requirements set forth by relevant authorities such as the FDA (Food and Drug...

As a Label Compliance Specialist at Amare Global, you will play a crucial role in ensuring that all product labels comply with regulatory requirements set forth by relevant authorities such as the FDA (Food and Drug Administration) and other regulatory bodies. Your attention to detail,  and ability to collaborate cross-functionally will contribute to the...

DivIHN (pronounced "divine") is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to...

*Title: Regulatory Affairs Specialist II *Location: Lake Forest, ILDuration: 12 Months*A detailed description of the position will be shared once we get your application**Regulatory Affairs Specialist II **Description*The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. In this role you will prepare documentation...

Role: Regulatory Specialist II Location: Lake Forest, IL, Santa Clara, CA, Boston, MA Duration: 6-12 Months RESPONSIBILITIES: Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR). Provides regulatory support for diagnostic product development and commercial diagnostic products. Develops...

Role: Regulatory Specialist IILocation: Lake Forest, IL, Santa Clara, CA, Boston, MADuration: 6-12 Months RESPONSIBILITIES:Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR).Provides regulatory support for diagnostic product development and commercial diagnostic products.Develops regulatory...

Role: Regulatory Specialist IILocation: Lake Forest, IL, Santa Clara, CA, Boston, MADuration: 6-12 Months RESPONSIBILITIES:Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR).Provides regulatory support for diagnostic product development and commercial diagnostic products.Develops regulatory...

Role: Regulatory Specialist IILocation: Lake Forest, IL, Santa Clara, CA, Boston, MADuration: 6-12 Months RESPONSIBILITIES:Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR).Provides regulatory support for diagnostic product development and commercial diagnostic products.Develops regulatory...

Position Title: Regulatory Specialist II Location: Lake Forest, IL,60045 Duration: 12 months. Shift Time: 8am - 5:00pm Job Responsibilities: Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR). Provides regulatory support for diagnostic product development and commercial diagnostic...

Job DescriptionJob Description·         The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit.  ·         In this role you will prepare documentation for EU Technical Files and international product registrations.  ·         This job description will be reviewed periodically and is...

Job DescriptionJob DescriptionFull time - Remote in US Office location: Lake Zurich, IL, Department:Document ManagementGeneral Description:The Document Management Specialist creates and supports the document management infrastructure life cycle.  The Document Management Specialist is a key member of Dovenmuehle that ensures all client documents are...

Job Description The Patient Care Tech reflects the mission, vision, and values of NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. Responsibilities: Performs a variety of clinical/patient care related...

Description This position will review, investigate, triage and recommend escalated compliant investigations for closure. As needed, the Postmarket Surveillance Specialist II (PSS-II) will coordinate investigations with departmental teams to identify complaint cause. The complaint investigation reports are routinely reviewed by external auditors and writing,...

This position will review, investigate, triage and recommend escalated compliant investigations for closure. As needed, the Postmarket Surveillance Specialist II (PSS-II) will coordinate investigations with departmental teams to identify complaint cause. The complaint investigation reports are routinely reviewed by external auditors and writing, knowledge...

Description This position will review, investigate, triage and recommend escalated compliant investigations for closure. As needed, the Postmarket Surveillance Specialist II (PSS-II) will coordinate investigations with departmental teams to identify complaint cause. The complaint investigation reports are routinely reviewed by external auditors and writing,...

This position will review, investigate, triage and recommend escalated compliant investigations for closure. As needed, the Postmarket Surveillance Specialist II (PSS-II) will coordinate investigations with departmental teams to identify complaint cause. The complaint investigation reports are routinely reviewed by external auditors and writing, knowledge of...

Location: Access Healthcare Multi-Specialty Group Position: Medical Assistant At AHMG, we provide clinical services, clerical support, and patient care in a forward-thinking environment. AHMG offers comprehensive benefits, paid time off. Join a team where your skills and ideas will make a difference in the health of our patients and the communities, we live...