Document Control Specialist
Company: Johnson & Johnson
Location: Santa Clara
Posted on: March 17, 2023
Job Description:
Job Description - Document Control Specialist (2306110527W)
Document Control Specialist - 2306110527W Description Robotics &
Digital Solutions, part of the Johnson & Johnson Family of
companies, is recruiting for a Document Control Specialist located
in Redwood City/Santa Clara, CA.Robotics & Digital Solutions is
part of Ethicon, Inc., a global leader in surgery with products and
solutions found in almost every operating room around the world.
Ethicon has made significant contributions to surgery for more than
100 years from creating the first sutures, to revolutionizing
surgery with minimally invasive procedures. Our continuing
dedication to Shape the Future of Surgery is built on our
dedication to help address the world's most pressing health care
issues and improve and save more lives. Through Ethicon's surgical
technologies and solutions including robotics, digital solutions,
sutures, staplers, energy devices, trocars and hemostats and our
commitment to treat serious medical conditions like obesity and
cancer worldwide, we deliver innovation to make a life-changing
impact. For more information, visit www.ethicon.comThe Specialist
will play an important role in implementing the document and change
control processes for changes to Documents and Records in PLM
systems such as Agile PLM. This role is responsible for providing
internal customers with mentorship in following document and change
control procedures.Are you interested in making a difference in a
thriving diverse company culture, that celebrates the uniqueness of
our employees and is committed to inclusion Apply today!Key
Responsibilities:
- Facilitate the change control process from initiation through
all workflows steps to implementation including review of completed
change orders for content and the approvals.
- Collaborate and provide mentorship to change owners, approvers,
and business partners.
- Review change orders and items for completeness and compliance
with QSR, ISO and internal template and procedure requirements in a
timely manner.
- Perform final incorporation of documentation revisions and
pre-release preparation of the document files associated with
approved change orders and ensure workflow activities are
completed.
- Consult with end users regarding problems in accessing
electronic content
- Select and/or verify required approvers of changes per
procedures.
- Assist in the preparation of document control metrics and
reports, including but not limited to periodic review process and
change order timeliness
- Communicate the status of changes.
- Support and recommend change control process improvements
including initiating procedural revisions.
- Support both internal and external audits, as well as quality
events (CAPA, NC, Audit findings), relating to document/change
control processes. Qualifications QualificationsEducation:
- Minimum of a Bachelor's, equivalent University Degree is
required; degree in a science-related subject or other related
fieldExperience and Skills:Required:
- Minimum 2 years of relevant work experience
- Proficient in Microsoft Suite (Outlook, Word, Excel, and
PowerPoint)
- Proven understanding of electronic documentation systems, data
retrieval and electronic file formats
- Ability to collaborate in an open office environment and
remotely with virtual teams while paying attention to detail
- Work successfully and in coordination with others and other
departments in achieving organizational goals
- Ability to coordinate, prioritize, and balance multiple
projects and tasks simultaneously
- Strong analytical, prioritization, communication, and
leadership skills
- Proven experience/knowledge with managing parts/BOM
structures/drawings
- Ability to work independently without supervision and in a
team
- Prompt in reporting for work and effectively and efficiently
uses their time to accomplish their job tasks
- Ability to meet project achievements and work in a fast-paced
environmentPreferred:
- Experience with Product Lifecycle Management (PLM) systems,
such as Agile PLM, ADAPTIV (Enovia platform), Windchill, and/or
equivalent PLM systems within a regulated industry - Direct
experience with Agile PLM is highly desired
- Familiarity and ability to apply Good Manufacturing Practices
(GMPs) documentation requirements, especially pertaining to quality
records and change control
- Medical Device, Pharmaceutical, and/or Biotech experience
- An understanding of FDA 21 CFR 820, ISO 13485 documentation
requirements, especially pertaining to document control, training,
quality records, and process control is preferred.
- Experience with MRP/ERP systems such as SAPOther:
- This position is located in Redwood City/Santa Clara, CA, and
requires less than 10% domestic travel.
- The anticipated base pay range for this position is:
- For California Bay Area Only, $68,900 to $96,600
- The Company maintains highly competitive, performance-based
compensation programs. Under current guidelines, this position is
eligible for an annual performance bonus in accordance with the
terms of the applicable plan. The annual performance bonus is a
cash bonus intended to provide an incentive to achieve annual
targeted results by rewarding for individual and the corporation's
performance over a calendar/ performance year. Bonuses are awarded
at the Company's discretion on an individual basis.
- Employees may be eligible to participate in Company employee
benefit programs such as health insurance, savings plan, pension
plan, disability plan, vacation pay, sick time, holiday pay, and
work, personal and family time off in accordance with the terms of
the applicable plans. Additional information can be found through
the link below.At Johnson & Johnson, we're on a mission to change
the trajectory of health for humanity. That starts by creating the
world's healthiest workforce. Through cutting-edge programs and
policies, we empower the physical, mental, emotional and financial
health of our employees and the ones they love. As such, candidates
offered employment must show proof of COVID-19 vaccination or
secure an approved accommodation prior to the commencement of
employment to support the well-being of our employees, their
families and the communities in which we live and work.Johnson &
Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, age, national origin, or protected veteran status
and will not be discriminated against on the basis of
disability.For more information on how we support the whole health
of our employees throughout their wellness, career and life
journey, please visit www.careers.jnj.com .]Johnson & Johnson is an
Affirmative Action and Equal Opportunity Employer. All qualified
applicants will receive considerationfor employment without regard
to race, color, religion, sex, sexual orientation, gender identity,
age, national origin,or protected veteran status and will not be
discriminated against on the basis of disability.andEqual
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individual with a disability, please check ourpage for information
on how to request an accommodation.Disability Assistance This site
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Keywords: Johnson & Johnson, Santa Clara , Document Control Specialist, Other , Santa Clara, California
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