Careers

Working at ZyVersa

ZyVersa is committed to restoring health and transforming lives of people with high unmet medical needs through innovation. If you are interested in working for a company that is passionate about making a difference, entrepreneurial, excited by a challenge, and driven to succeed, we want to hear from you.

We offer competitive compensation and a comprehensive benefits package, including medical, dental, 401k and more.

Available positions are listed below.

Description:
Responsible for Quality Assurance, cGMP and GCP compliance for ZyVersa activities and products. Establishes, monitors, and maintains Standard Operating Procedures. Interacts extensively with off-site vendors including but not limited to manufacturing/packaging vendors, contract manufacturers, and clinical research organizations. Maintains manufacturing and control documents in compliance with cGMPs and regulatory submissions, manages the corporate change control program.

Responsibilities:

  • Responsible for cGMP and GCP compliance of ZyVersa Therapeutics.
  • Participates in establishing quality standards for ZyVersa and communicating these quality standards to vendors.
  • Establish and implement audit programs system for ZyVersa Therapeutics.
  • Leads mock inspections and other efforts in support of FDA approval.
  • Oversees GMP and GCP audits
  • Assures critical documentation is maintained in an updated and cGMP-compliant status.
  • Create, maintain and manage the processes for the implementation of SOPs and internal training programs.
  • Serves as the Quality Assurance representative on business programs.
  • Provide support to the internal and external customers in regard to quality assurance issues.
  • Participates in the development of quality agreements with third party manufacturers.
  • Plans and executes cGMP and quality system upgrades required.

Qualifications:

  • Bachelor's degree in scientific discipline. Preference for advanced degree in science related area
  • Minimum 5+ years pharmaceutical quality assurance experience.
  • Experience in implementation of both cGMP and GCP compliance

Related Skills and Experience:

  • Good analytical and interpretative skills with the ability to anticipate regulatory trends and emerging issues
  • Able to travel as a function of the role.
  • Ability to quickly identify crucial situations and take appropriate action
  • Proven experience with interfacing with FDA, and other regulatory agencies.
  • Demonstrated ability to commit to decisions that are sometimes difficult or controversial.
  • Able to use appropriate methods and interpersonal styles to develop, motivate, and guide a team in the direction of positive outcomes and to meet business objectives.

Location: Philadelphia, PA metropolitan area

The above statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities.

ZyVersa Therapeutics is an Equal Opportunity and Affirmative Action Employer committed to a culturally diverse workforce. All qualified candidates will receive consideration without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital, domestic partnership or civil union status, sex, gender identity or expression, sexual orientation, disability, veteran status, violence victim status or any other characteristic protected by law.

Assistant Director, Quality Assurance: Apply Now

Description:

To provide administrative support to ensure efficient operation of the office. Support senior staff through a variety of tasks related to organization and communication. Responsible for confidential and time sensitive material. Ability to effectively communicate via phone and email ensuring that all duties are completed accurately and delivered with high quality and in a timely manner. Rely on experience and judgment to plan and accomplish goals and a wide degree of creativity and latitude is expected. Reports to the CSO, V.P of Research and Development.

Responsibilities:

  • Ability to work independently in a virtual pharmaceutical organization.
  • Drafting letters and documents
  • Initiating discussions and introductions through telecommunications.
  • Maintains appointment schedules, scheduling meetings, conferences, teleconferences, and travel.
  • Welcomes guests and customers; answering or directing inquiries.
  • Maintains confidence and protects operations by keeping information confidential.
  • Prepares, modifies and finalize reports by transcribing, formatting, and editing text, data, and graphics
  • Secures information by completing assigned IT related activities.
  • Develops and maintains filing and retrieval systems.
  • Maintains office supplies and equipment inventory; expediting orders; and verifying receipt of supplies.
  • Ensures operation of office equipment; completing preventive maintenance; troubleshooting; and scheduling repairs

Qualifications:

Work history in a pharmaceutical development setting is preferred. Demonstrated writing and reporting skills. Moderate to advanced skills in Microsoft Office Suite are required. Proven organization, time management, and communication experience. Experience in the preparation of presentations and complex documents. History of scheduling conferences, preparing itineraries, arranging lodging, travel and services.

Related Experience:

  • Proven administrative or assistant experience
  • Knowledge of office management systems and procedures
  • Excellent time management skills and ability to multi-task and prioritize work
  • Attention to detail and problem-solving skills
  • Excellent written and verbal communication skills
  • Strong organizational and planning skills
  • At least 5 years of experience in the field or in a related area
  • High school diploma or equivalent; college degree preferred

Location: Philadelphia, PA metropolitan area

The above statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities.

ZyVersa Therapeutics is an Equal Opportunity and Affirmative Action Employer committed to a culturally diverse workforce. All qualified candidates will receive consideration without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital, domestic partnership or civil union status, sex, gender identity or expression, sexual orientation, disability, veteran status, violence victim status or any other characteristic protected by law.

Administrative Assistant: Apply Now

Description:

The Project Manager will be responsible for overseeing the execution of work plans for delivery of new products. The reporting to the CSO, V.P of Research and Development, the Project Manager will work collaboratively with all functional departments and consultants to coordinate and integrate the successful management of assigned assets through all levels of development to NDA. The position will be responsible to develop projects plans in terms of status, budget, and time-line. The successful candidate will be knowledgeable of the overall development of pharmaceutical agents and able to fully integrate multidisciplinary functions into a cohesive plan.

Responsibilities:

  • Ability to work independently in a virtual pharmaceutical organization.
  • The timely recognition, reporting, and resolution of project issues through effective application of the collective expertise of the core team, along with any necessary additional experts.
  • The development of a range of options and recommendations for resolution to be presented to Management.
  • The ability to manage outsourced service providers, including CROs, and manufacturing service providers.
  • Scheduling and facilitating team meetings, for effective team and management communications.
  • Attends functional meetings; prepares minutes, presentations; and documents internal processes.
  • Creating and maintaining detailed project plans (MS Project) and budgets.

Qualifications:

The position requires a BS in Life Science with 7-10 years of relevant experience, including both project management and pharmaceutical industry development experience. Excellent verbal and written communication skills are essential. Periodic travel is anticipated.

Related Experience:

  • Demonstrated knowledge of project management processes and controls
  • Familiarity with pharmaceutical development requirements
  • Working knowledge of pharmaceutical regulations (cGMP, cGLP, cGCP)
  • Familiarity with Microsoft Word, Excel, and Project; Adobe Acrobat

Location: Philadelphia, PA metropolitan area

The above statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities.

ZyVersa Therapeutics is an Equal Opportunity and Affirmative Action Employer committed to a culturally diverse workforce. All qualified candidates will receive consideration without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital, domestic partnership or civil union status, sex, gender identity or expression, sexual orientation, disability, veteran status, violence victim status or any other characteristic protected by law.

Project Manager: Apply Now