Skip to content

Open nowFirst seen 2 days ago

Lead IT Administrator - Quality Managemant System

RxCloud86 open roles

Where
Remote, Oregon, United States
Work mode
Remote
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowLead IT Administrator - Quality Managemant SystemRxCloud · Remote, Oregon, United States
  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on RxCloud's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

11.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.4%3 days
  3. 11.8%7 days
  4. 18.6%14 days
  5. 35.6%30 days
  6. 45.1%60 days
This job: first seen 2 days ago

The posting

As an integral member of the Enterprise Quality Assurance management team the Lead Quality Systems Administrator oversees the development, implementation and maintenance of the Enterprise quality system at the assigned divisions, with the guidance and support from the Quality Assurance Directors and VPs. The QA Manager provides day-to-day direction, support and leadership to the QA associates and ensures that the team has adequate resources to meet its responsibilities. Additionally, this role provides QA input and advice to the management teams of the assigned business units (i.e., programs and/or departments) and assures the business units remain compliant with established procedures, client contractual agreements, EQA policies and procedures, and applicable regulations and guidelines by scheduling routine program/department audits and process/system audits to ensure client contractual agreements and EQA standards are met. This position is expected to interact directly with clients/sponsors, vendors and regulatory inspectors. The Lead Quality Systems Administrator should be highly proficient in eQMS technical configuration, understanding development processes, and maintaining infrastructure hygiene (i.e. ensuring eQMS subscription has adequate storage space and projecting future needs). The Lead Admin will also be responsible for managing up to 3 additional administrators with varying levels of experience, monitoring their performance, and ensuring completion of assigned administration duties. Where junior resources are added to the team, the Lead Admin is expected to provide education, training, and guidance in developing their skillset. Will act as the final level of escalation for complex technical issues impacting service availability. Work with project managers to coordinate and plan project tasks and resources. Lead Administrator, QMS should be highly proficient in eQMS technical configuration, understanding development processes, and maintaining infrastructure hygiene.

PRIMARY DUTIES AND RESPONSIBILITIES:

  • Oversee Quality Systems administration team, ensuring timely completion of assigned duties
  • Manage queue of requests from eQMS userbase through ServiceNow ticketing, tracking metrics, and reporting on overall current state of eQMS development
  • Creation of presentation materials, demonstrating timelines for assigned projects, milestones, and delivery of value
  • Host and coordinate external audits by sponsors/clients and/or regulatory agencies.
  • Coordinate collation of responses and corrective actions from external audits with relevant program and/or departments to ensure timely resolution of observations and issuance of responses.
  • Leverage QMS Engineering experience to drive development around best practices and optimal system performance.
  • Works closely with IT / QA to manage risk, verification, quality, and validation plans.
  • Maintain accurate records of internal and external audit files, including schedules, audit plans, audit evidence and audit reports. Assist in the archiving of QA documents.
  • Implement Quality Assurance procedures as per internal requirements and/or client contractual requirements;
  • Organize, schedule and conduct internal audits for the various programs and/or departments (as assigned by the Director, QA) to ensure client requirements (e.g., procedural steps, operational reports and AE reporting, etc.) are met and company policies and procedures are complied with;
  • Ensure program/department audits and internal process/system audits are scheduled in advance and reflected in the QA audit calendar;
  • Analyze and evaluate available data and prepare or review written reports of audit findings and observations;
  • Keep QA management up to date on findings and status of corrective/preventive actions;
  • Manage the CAPA process for the assigned programs/departments by ensuring that non-conformance and other reportable events as well as CAPA reports are recorded, followed-up, tracked and trended;
  • Conducts periodic Quality Management Review (QMR) meetings with Patient Support Program Management Teams and related functional areas to review key quality metrics, discuss trends/issues and coordinate quality improvement initiatives.
  • Implement continual process improvements related to assigned program/departmental processes and/or internal processes as required;
  • Manage the controlled documents (Policies, SOPs, WIs and Forms) request, review and issuance work flow by actively liaising with each program/department management as assigned, and coordinating with the respective programs/department managers or designates to ensure the controlled documents are generated and finalized in a timely manner;
  • Understand program/project roadmap and key milestones regarding criticality, downstream impact if dates are missed and determine alternative/mitigating actions.
  • Provide timely, concise communications to functional and executive leadership regarding project status and pending issues.
  • Build consensus among multiple functional and technical leads relative to project audit scope, task execution, staffing and issue resolution.
  • Recommend corrective actions to program/department leadership when project deliverables deviate from the work plan with the assistance of team members.
  • Interact with project sponsors, stakeholders, vendors and various project members to ensure that specified business needs are met; assists in the post-implementation analysis to ensure that requirements are fulfilled.
  • Serve as a resource to internal stakeholders for the interpretation and application of regulations and applicable guidelines;
  • In coordination with the Director, Quality Assurance, prepare QA budget and manage departmental expenses;
  • Work with the rest of the QA management team in the development/revision and implementation of QA policies and procedures as required;
  • Understand and apply company Confidentiality and Privacy Agreements
  • The Quality Assurance Manager may also be assigned other duties and tasks as required from time to time by the Director, Quality Assurance.
  • Travels up to 20% of the time.

What your background should look like

  • Bachelor of Science Degree in a scientific, healthcare or pharmaceutical field, or equivalent.
  • Minimum of 5 7 years experience in the healthcare, pharmaceutical or biotechnology industry (or similar), preferably in a quality assurance or quality control function.
  • Minimum of 5 years experience in hosting external audits and management of multiple projects (planning, implementation, management and monitoring) including budget, resource planning, Key Performance Indicators, etc.;
  • Industry certification in Quality or Clinical Research (e.g., CQA, RQAP-GxP, CCRC, CCRA, CCRP, etc.) is an asset.
  • Responsible and accountable for success/delivery of quality needs for QMS system
  • Responsible for managing 1-3 QMS engineer resources in delivery of high-quality business/customer service and consultancy to QA departments
  • Experience coaching junior/entry-level resources, ability to create development plans, and foster growth and QA knowledge in reports
  • Experience in executive reporting and developing product roadmaps to communicate QMS growth strategy
  • Quality or quality parallel professionals with 5-7 years experience, with extensive experience in a QMS System (i.e. MasterControl, TrackWise, Veeva)
  • Extensive knowledge of GxP, GDP, GMP, ISO 9001 and related Quality Standards

MINIMUM SKILLS, KNOWLEDGE AND ABILITY REQUIREMENTS:

  • Strong knowledge in quality assurance principles and quality management, including design and operation of effective quality and regulatory compliance programs;
  • Advanced knowledge of root cause analysis and CAPA investigations;
  • Ability to develop and implement customized Quality Assurance procedures specified by internal/external industry specification;
  • Advanced analytical, conceptual and problem solving skills to evaluate business; problems and apply knowledge to identify appropriate solutions;
  • Well-developed leadership, analytical, and decision making skills, with an aptitude to appropriately apply scientific, regulatory and administrative knowledge to accomplish department and company goals.
  • Superior skills in planning, organization and managing multiple priorities yet being flexible, adaptable and able to respond to changing needs.
  • Proven conflict management skills with the ability to provide leadership to others in response to situations and to escalate more critical decisions when relevant.
  • Excellent verbal and written communication skills, work well in an interdependent team environment, and promote positive, respectful professional relationships. Proficient in writing reports containing technical information;
  • Effective presentation skills and experienced in the development of training courses and materials.
  • Proven ability to organize time, set priorities and multi-task in order to meet various competing work deadlines;
  • Strong attention to details and data analysis skills;
  • Ability to work independently and in a team environment;
  • Strong proficiency in Microsoft applications (Word, Excel, PowerPoint, , Outlook), Adobe Acrobat.
From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against RxCloud's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.
  3. We apply on RxCloud's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.
  4. Every reply, sorted

    RxCloud's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.
  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.