3 Days (580)

Civica Rx•Petersburg, VA

6d•Onsite

About The Position

The Manufacturing Support Supervisor will play a role in facility start-up and commercialization, with primary responsibilities focused on supporting daily manufacturing operations and the timely production of pharmaceuticals at the Civica site in Petersburg, VA. This position will hire, develop, and support a team of manufacturing associates through equipment qualifications, identifying and improving processes, operating manufacturing equipment, and owning documentation. This position will provide new process training to the manufacturing team to achieve efficient, cost-effective, safe, and compliant production of high-quality injectable products in line with the Civica culture and vision for what is in the best interest of the patient. This is a 6:00 AM – 6:30 PM, 2-2-3 work schedule.

Requirements

Bachelor's degree with 4+ years of demonstrated ability in a cGMP FDA, cGMP, ISO, or other regulated production environment. An associate’s degree and 6 years of cGMP production experience may be considered.
Experience with Autoclaves and Parts Washers.
1+ years of supervisory experience in a GMP manufacturing environment.
Experience in a process improvement environment, including change management and leading teams.
Strong writing and documentation skills.
Self-directed with effective analytical and problem-solving skills.
Strong interpersonal, collaboration, communication, and leadership skills.

Nice To Haves

Lean Manufacturing/Six Sigma Green Belt Certification preferred.

Responsibilities

Actively participate in new equipment and process qualifications.
Serve as the escalation point for their group, take accountability and ownership for business, technical, and compliance decisions.
Maintain inspection readiness and serve as SME during inspection tours.
Ensure staff are appropriately trained and qualified for the activities they perform prior to execution.
Ensure systems and processes are properly executed and maintained to ensure staff’s safety, product quality, and continuity of supply.
Develop and create standard operating procedures, specifications, and other forms of governing documents to delineate manufacturing process requirements according to qualification, compliance, and business requirements.
Ensure that the Manufacturing organization operates to meet the requirements of approved production plans at minimum costs within established quality limits and in accordance with FDA, cGMP, ISO, and OSHA requirements.
Identify opportunities to improve customer service, quality, safety performance, process efficiencies, or otherwise reduce manufacturing costs by using effective project management, cost control techniques, and Lean Manufacturing tools and techniques.
Mentor, coach, and teach Manufacturing Associates in the use of change management/control techniques to ensure timely completion of projects.
Utilize scientific methods and statistical tools to perform investigations, root cause analyses, and impact assessments in support of the timely resolution of deviations/discrepancies related to Manufacturing.
Identify corrective and preventive actions (CAPA) and lead projects to completion within project timelines.
Verify the effectiveness of CAPA by post-project data collection and analysis.
Flex schedule to meet commitments and achieve milestones related to projects, production, and other demands of the role.
Maintain accuracy of and approve staff’s timecards.