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Career Opportunity: Job Title: Coord 2, Quality Document Sys Management About CodeForce 360 Making a career choice is amongst the most critical choices one can make, and it's important for the choice to be calculated with factors such as a company's run of success since its inception and more. But, when you come across a company that has reputation proven with nothing but an illustrious run of success since the day it began, you don't need to think of anything else. That's precisely what some of our employees and prospective employees think when they came across CodeForce 360. Position Overview Coord 2, Quality Document Sys Management Must have:
- Excellent professional/business writing skills and the ability to communicate correctly and concisely in English
- Experience with technical writing or documentation review
- Demonstrated proficiency with MS Office skills, particularly in PowerPoint, Excel, and Word. Proficiency with SharePoint, Jira, and Confluence preferred.
- The Project Coordinator, Compliance and Documentation, supports the Global Customer Services (GCS) organization within CLIENT's Medication Management Solutions (MMS) Business Unit.
- In collaboration with SMEs in GCS and other cross-functional teams, this role serves the GCS Readiness function in ensuring documentation, process and procedural compliance with quality and regulatory requirements.
- The Project Coordinator is responsible for the collection/creation, updating and verification of all GCS content across the Dispensing and STS product areas.
- In addition, the role will manage content workflows through the Veeva system to ensure approved, compliant product information is released to GCS in a timely and accurate manner.
- Lastly, this role will be responsible for overseeing and contributing to the creation and maintenance of relevant GCS SOP and SWI documentation in compliance with all applicable quality requirements.
- The Project Coordinator role requires solid project management skills, attention to detail, strong process execution and analytical skills.
- This role will support GCS Implementation by assuring that the documentation that is foundation to the implementation and upgrade of Dispensing and STS products is current, accurate and complete.
- He/she will create and curate the GCS implementation documentation for the Dispensing and STS Portfolio of products.
- Actively participate in GCS compliance initiatives with Readiness and Quality project teams.
- Assists GCS Readiness Project Managers in preparing procedures, work instructions, and GCS documentation.
- Ensures GCS documents are produced in accordance with corporate/BU procedures, and regulatory standard/guidance. Assists with writing content when required.
- Assists GCS Readiness project managers with documentation and process reviews, including scheduling meetings, facilitating SME input, collating documentation input, and tracking completion of deliverables in accordance with standard project management practices.
- Plans, coordinates, and executes all Veeva Vault activities to ensure compliance with regulations and standard work instructions procedures
- Creates and maintains documentation fS on how to use Veeva Vault
- Attains and maintains required expertise in all databases that house product data for the platform (Veeva Vault, SAP, SharePoint)
- Attains mastery of all CLIENT processes for governing GCS documentation
- Serves as subject matter expert and resource fS on documentation, ensuring GCS documentation is controlled and approved, and make optimizations as needed.
- Identifies opportunities to streamline or improve processes
- Excellent professional/business writing skills and the ability to communicate correctly and concisely in English
- Strong technical skills and experience with using a document management system like Veeva Vault or SAP
- Ability to understand system operations and dependencies to effectively set-up, manage, and troubleshoot problems with a documentation management system
- Ability to gain new technical skills quickly
- Strong customer service skills and positive attitude
- Ability to communicate complex technical concepts in layman's terms
- Advanced skills with Microsoft Office products
- Ability to meet tight deadlines and handle changing priorities
- Bachelor's Degree in Engineering, Technology, or Life Sciences preferred.
- Two or more years of experience in project management
- Prior experience within a regulated industry (e.g., medical device, pharma, automotive, aerospace) is preferred
- Managed/supported projects cross-functionally in an iterative, fast paced environment
- Experience with technical writing or documentation review preferred
- Excellent verbal and written communication skills required
- Strong analytical, problem-solving, and interpersonal skills
- High attention to detail while managing multiple complex deliverables and stakeholder groups
- Ability to learn quickly, deal with ambiguity, take initiative and achieve results
- Demonstrated proficiency with MS Office skills, particularly in PowerPoint, Excel, and Word. Proficiency with SharePoint, Jira, and Confluence preferred.
- Proven organization and time management skills
- Location: prefer San Diego candidate or candidate located in Pacific or Mountain Time Zones
- ID: #49385857
- State: California San diego 92130 San diego USA
- City: San diego
- Salary: USD TBD TBD
- Job type: Contract
- Showed: 2023-03-01
- Deadline: 2023-04-29
- Category: Et cetera