Associate Director Automation
Company: Civica Rx
Location: Petersburg
Posted on: November 10, 2024
Job Description:
About Civica: Over the past two decades, shortages of generic,
injectable medications critical to the lifesaving work of hospitals
in the United States have become commonplace and have reached an
all time high. Over 300 essential medications are reported to be in
shortage, according to industry and FDA reports. "Race to the
bottom" pricing of mostly sterile injectable medications,
manufacturing challenges and predatory pricing are both the causes
and results. Who suffers most? Patients. Civica is a 501(c)(4)
social welfare organization established in 2018 by health systems
(CommonSpirit Health, HCA Healthcare, Intermountain Healthcare,
Mayo Clinic, Providence St. Joseph Health, SSM Health, and Trinity
Health) and philanthropies (Gary and Mary West Foundation, Laura
and John Arnold Foundation, and Peterson Center on Healthcare) to
reduce chronic generic drug shortages and related high prices in
the United States. An experienced team of health care and
pharmaceutical industry leaders leads the organization. Today, more
than 55 health systems have joined Civica. They represent over
1,500 hospitals and over 30 percent of all U.S. hospital beds.
Civica has also supplied the U.S. Department of Veteran's Affairs,
the U.S. Department of Defense, and the U.S. Strategic National
Stockpile of essential medicines. Since established, the #1 Policy
for the Civica team has been "Do What Is in the Best Interest of
Patients." Civica has expanded its mission beyond the hospital
setting to include lowering the cost of medications at the pharmacy
counter. It has launched a sister organization, CivicaScript, to
enter the retail pharmacy market partnering with Blue Cross Blue
Shield entities and others with the goal of reducing select high
cost generic drugs where market forces are not working to control
drug costs. More recently, Civica announced plans to develop,
manufacture and deliver affordable biosimilar insulin, The
consistent availability of affordable insulin will benefit people
who ration their care or who have been forced to choose between
this life-sustaining medicine and living expenses. Those who are
uninsured or underinsured often pay the most out of pocket for
their medications. Long- and short-acting insulins will be produced
and available in both vials and pre-filled pens - at no more than
$30 per vial and no more than $55 for a pack of five pens. Learn
more about Civica's plans and progress at www.civicarx.org Job
Description The Associate Director of Automation and MES is
responsible for developing and implementing the Automation strategy
and oversees a site-based team accountable for the development,
implementation, and operational compliance of the Civica Petersburg
process automation philosophy and associated industrial control
systems (ICS) including facility, utility, and manufacturing
processes, as well as supporting infrastructures. The Plant ICS
system includes: DCS, SCADA, PLC, BMS, EMS and data systems such as
historian and analytics solutions. As the functional leader, you
have the ability to make decisions, and are capable of setting and
balancing priorities. You must be able to manage multiple projects
with frequent changes and are able to coordinate and manage project
activities while involving cross-functional partners. You have a
willingness to perform "hands-on" work in a dynamic, fast-paced
start up environment. Incumbent provides technical expertise on
Manufacturing and Compliance standards and processes to team
members; and provides input on strategy to key business leaders.
Essential Duties and Responsibilities:
- Develop the automation strategy for the site.
- Lead the Automation Engineering function supporting mission
critical Automation Systems in the manufacturing of commercial and
clinical products. The scope of this group will include support of
the following systems:
- Data Historians
- Central Monitoring Systems
- Process Automation and Building Management Systems
- SCADA and PLC systems
- Accountable for the delivery of all aspects of plant
execution/operations systems to support site commissioning,
validation, and on-going safety, compliance, and quality
manufacturing.
- Lead and manage the group of automation engineers and represent
the Automation Engineering function to other partner groups such as
IT, Quality, Validation; Manufacturing, Engineering & Technical
Services, ensuring the quality of work and appropriate resources
are in place to support ongoing initiatives, operations and
projects requiring Automation Engineering Support
- Support Manufacturing and Operations by providing strategic
direction and tactical support. Troubleshoot day-to-day issues,
assigning personnel as necessary to provide comprehensive
solutions.
- Set and drive strategic priorities for the holistic systems
technology landscape for the site, including but not limited to
oversight of new plants/ facilities, changes to plant
execution/operations systems, automation engineering systems,
develop and maintain validation lifecycle strategy etc. Responsible
to implement, validate, maintain, and govern S95/S88 Standards,
Libraries, Interfaces & Systems.
- Accountable to develop and manage the Leads along with a high
performing team to deliver on above responsibilities. Create and
sustain a culture of innovation, quality, compliance,
accountability, employee engagement, collaboration, diversity, and
inclusion.
- Responsible for inspection/audit readiness (internal and
external) in relation to the Automation systems. Also accountable
for adherence to cybersecurity corporate requirements, all
engineering aspects of data integrity, and provide leadership
support for alarm management.
- Mentor, coach, train and evaluate a team of automation
engineers.
- Implement automation policies and related procedures based on
regulations and industry standards.
- Provide oversight in the authoring and review of SOPs and
system support.
- Analyze operational process problems and recommend appropriate
corrective and preventative actions.
- Participate in the site wide teams to provide cybersecurity
alignment and direction.
- Effectively interact and collaborate with cross-functional
departments and vendors to drive automation deliverables.
- Establish and maintain continuous improvement projects.
- Participate in regulatory inspections (e.g. FDA, DEA) as a
Subject Matter Expert (SME).
- Demonstrates strong leadership, motivation, teambuilding,
communication, and advanced coaching skills that instill a strong
sense of mission in a team environment across all levels of
organization.
- Forecasts and adheres to departmental budget, and responsibly
manages resources.
- Implement a culture of continuous improvement and ensure the
adoption of best practices. Ensure safety is integral.
- Ensure safety is integral to all activities. Basic
Qualifications and Capabilities:
- A minimum of a bachelor's degree or similar technical degree is
required.
- 10+ year's progressive experience in automation or related role
in the pharmaceutical industry.
- 5+ years of subject matter expertise with automation
execution.
- Experience with writing software test plans, user requirements,
and system design documents.
- Strong knowledge of programming and troubleshooting Rockwell or
SiemensPLCs and Rockwell or Siemens FTView, GE iFix, and/or
Wonderware System Platform HMIs.
- Strong knowledge of Computerized Systems, Compliance
regulations and standards.
- Assist and provide resources in various stages of the
engineering project lifecycle from conceptual design, detailed
design, specification, implementation, commissioning,
qualification, trouble-shooting and continuous improvement of
automation and instrumentation for the sterile injectable
industry.
- Collaborate with functional and discipline heads and leads to
develop solutions to issues that are immediately impacting business
needs. Collaborates effectively with Operations, Quality,
Regulatory, Process Development, Supply Chain, and other key groups
involved in GMP manufacturing.
- Demonstrates strong leadership, motivation, teambuilding,
communication, and advanced coaching skills that instill a strong
sense of mission in a team environment across all levels of
organization.
- Demonstrates excellent planning and organizational skills, with
the ability to balance production and maintenance needs.
- Excellent project management and time management capabilities;
with the ability to partner and influence across a matrixed
environment. Excellent communication skills; verbal & written.
- Forecasts and adheres to departmental budget, and responsibly
manages cost center resources. Preferred Qualifications:
- Knowledge of Database/Historian (SQL, AVEVA PI).
- Knowledge of Vmware and virtualization
- Basic networking knowledge.
- Knowledge of systems such as Allen Bradley PLC platforms,
Johnson Controls, Amega or DeltaV, SCADA systems, PI Historian,
Siemens PLC S7, iFix, iHistorian, Industrial Ethernet networks,
Profibus and AS-I networks.
- Knowledge and understanding of Data Integrity and how it
applies to the BioTech Industry with specific focus on guidelines
from the FDA.
- Exposure to batch and continuous processes found in the
pharmaceutical and Biotech Industries is preferred.
- Experience with S88 and ASTM 2500 principles would be an
advantage.
- Exceptional organizational and teamwork skills are required to
be successful in this dynamic environment with changing
priorities.
- Experience with regulatory inspections.
- Demonstrated management and delivery of large capital
projects.
- Subject matter expertise with Computerized Systems Validation
(CSV)
- Previous experience/best practices implementing and using
continuous improvement/lean tools such as; Six Sigma, 5-S, Lean
Manufacturing, Transactional Lean, etc. PandoLogic. Keywords:
Automation Director, Location: Petersburg, VA - 23803 , PL:
595171079
Keywords: Civica Rx, Newport News , Associate Director Automation, Executive , Petersburg, Virginia
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