Planet Pharma
Job Description
The Senior Quality Coordinator is part of the Novato Quality Leadership Team (NQLT) reporting to the Head of Site Quality in Novato, California. The role is responsible for supporting MSA, NDA and SOW for the head of Global Quality Assurance, Novato Site Quality Head and Head of Product Quality Lifecycle Management Head.
The Senior Quality Coordinator will work in a fast-paced environment that requires efficient and timely completion of duties. This role also supports the Novato Site Head of quality in developing and managing visual displays, metrics pertinent Novato Quality.
This position requires critical thinking ability, influencing, collaboration, multi-tasking, independent execution, and leadership skills.
KEY RESPONSIBILITIES
-Develop and maintain visual displays for monitoring key performance indicators for Novato Quality Leadership team.
-Manage department budget and associated processes.
-Assist NQLT in the creation and maintenance of RACIs and SLAs
-Develop and implement NQLT sponsored projects and timelines. Serve as project manager as needed.
-Create presentation slide decks as needed.
-Attending NQLT staff meetings and serving as a scribe to capture decisions and action log. Maintain NQLT action log.
-Initiate and process MSA/NDA and SOW contracts in support of Global Quality Assurance, of Product Quality Lifecycle Management and Novato Site Quality Heads. Onboard New Suppliers in Coupa
-Proactively coordinate, create, and manage Novato site visit agenda and itinerary for the Chief Quality Officer (SVP)
-Create and maintain distribution lists for Novato Quality. Develop a system for maintaining the lists current.
-Manage budget for, plan, schedule and facilitate site quality engagement events
-Provide proactive support in managing the Quality Site Head's calendar, including scheduling meetings, coordinating appointments, and ensuring optimal time allocation for business priorities.
-Perform other duties as assigned.
REQUIREMENTS
-BA/BS in life sciences or related field
-Excellent interpersonal and communication skills (written & verbal) and ability to influence diverse stakeholders and drive accountability and decision-making cross functionally and at all levels.
-Demonstrated ability to partner with other functional groups to achieve business objectives.
-Demonstrated ability to work independently and effectively.
-Demonstrated ability to drive continuous improvement and operating with a Lean and Agile mindset.
-Experience in project management is a plus.
-Ability to create slide presentations.
-Ability to work in a fast-paced environment.
-Results oriented; effectively manage multiple projects efficiently.
-Demonstrated knowledge in data analytics and visual management tools required.
-Experienced in using business related AI tools such as Co-pilot
-Proficiency in Microsoft office Suites required.
-2+ years' experience in Biotechnology, Pharmaceutical or other regulatory industry preferred but not required.
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it's from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
The Senior Quality Coordinator is part of the Novato Quality Leadership Team (NQLT) reporting to the Head of Site Quality in Novato, California. The role is responsible for supporting MSA, NDA and SOW for the head of Global Quality Assurance, Novato Site Quality Head and Head of Product Quality Lifecycle Management Head.
The Senior Quality Coordinator will work in a fast-paced environment that requires efficient and timely completion of duties. This role also supports the Novato Site Head of quality in developing and managing visual displays, metrics pertinent Novato Quality.
This position requires critical thinking ability, influencing, collaboration, multi-tasking, independent execution, and leadership skills.
KEY RESPONSIBILITIES
-Develop and maintain visual displays for monitoring key performance indicators for Novato Quality Leadership team.
-Manage department budget and associated processes.
-Assist NQLT in the creation and maintenance of RACIs and SLAs
-Develop and implement NQLT sponsored projects and timelines. Serve as project manager as needed.
-Create presentation slide decks as needed.
-Attending NQLT staff meetings and serving as a scribe to capture decisions and action log. Maintain NQLT action log.
-Initiate and process MSA/NDA and SOW contracts in support of Global Quality Assurance, of Product Quality Lifecycle Management and Novato Site Quality Heads. Onboard New Suppliers in Coupa
-Proactively coordinate, create, and manage Novato site visit agenda and itinerary for the Chief Quality Officer (SVP)
-Create and maintain distribution lists for Novato Quality. Develop a system for maintaining the lists current.
-Manage budget for, plan, schedule and facilitate site quality engagement events
-Provide proactive support in managing the Quality Site Head's calendar, including scheduling meetings, coordinating appointments, and ensuring optimal time allocation for business priorities.
-Perform other duties as assigned.
REQUIREMENTS
-BA/BS in life sciences or related field
-Excellent interpersonal and communication skills (written & verbal) and ability to influence diverse stakeholders and drive accountability and decision-making cross functionally and at all levels.
-Demonstrated ability to partner with other functional groups to achieve business objectives.
-Demonstrated ability to work independently and effectively.
-Demonstrated ability to drive continuous improvement and operating with a Lean and Agile mindset.
-Experience in project management is a plus.
-Ability to create slide presentations.
-Ability to work in a fast-paced environment.
-Results oriented; effectively manage multiple projects efficiently.
-Demonstrated knowledge in data analytics and visual management tools required.
-Experienced in using business related AI tools such as Co-pilot
-Proficiency in Microsoft office Suites required.
-2+ years' experience in Biotechnology, Pharmaceutical or other regulatory industry preferred but not required.
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it's from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.