Program Manager

  • Full-time

Company Description

On December 31st, 2020 Innova Medical, Inc. acquired MPS Medical to expand its U.S production of COVID-19 antigen test kits, producing over 4 million SARS-CoV-2 Antigen Rapid Qualitative Tests per day.  Currently, Innova Medical Group, Inc. is the world’s largest manufacturer of rapid antigen test kits and leader in COVID-19 testing solutions arena.

Innova Medical Group, Inc. achieves to deliver better global health outcomes with its deep expertise in testing and unique offerings in diagnostic medical devices and services that help tackle some of the world’s most challenging healthcare problems. Alongside of COVID-19 solutions, Innova specializes in innovative screening, testing and diagnostics for cancer, heart disease, arterial calcification, stroke, and virus detection focused on infectious disease.

In this role coordinates activities related to production, personnel handling, quality assurance, material requesting and internal customer service in product manufacturing. This includes activities area assigned in the clean room and packaging area

www.innovamedgroup.com

www.mpsmedical-inc.com

Job Description

  • Coordinates MPS projects in accordance with policies, principles, and procedures established by the company.
  • Develops plans for efficient use of materials, machines, and human resources.
  • Reviews MPS costs and product quality and modifies required outputs to maintain and enhance profitability.
  • Confers with the company CEO and other management personnel to review achievements and discuss required changes in goals or objectives resulting from current status and conditions.
  • Ensure that all customer expectations are met or exceeded.
  • Support the design and implementation of validation studies on specified customer equipment / process to ensure consistency of data production and concurrence with manufacturer and FDA/ISO standards.
  • Supports the reviews protocols to national and international standards. 
  • Serves as liaison / team member with QA, Regulatory Affairs, Research and Development and Manufacturing departments.
  • Manages/supports and directs as needed, the activities for MPS Products
  • Responsibilities include assigning work, appraising employee performance, addressing complaints and resolving internal/external problems.
  • Other responsibilities and tasks assigned by CEO.

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Expertise and familiarity with PC applications software and manufacturing systems software.
  • Working knowledge of the medical device industry regulatory standards.
  • Multi-year experience in contamination control.
  • Requires a bachelor’s degree or significant verifiable experience in the medical device or other regulated industry.
  • Must possess more than basic mathematical skills.
  • Position requires a strong ability to identify opportunities for improvement and implement changes.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Requires the ability to communicate effectively, written and verbal as well as effective people skills.

Additional Information

PHYSICAL DEMANDS –Reasonable accommodations may be made to enable individuals with disabilities to perform the following essential physical demands:

  • Physically able to sit, stand and walk for extended periods of time.
  • Able to move about on foot; walk up and down stairs repeatedly as needed.
  • Clarity of vision at 20 inches or more; able to view a computer monitor for extended periods of time.