Offer summary

Qualifications:

Bachelor’s degree in science or equivalent experience, 7+ years of GxP experience in pharmaceutical industry, Working knowledge of quality risk assessment, Extensive knowledge of GMP regulations, Strong technical writing and software skills.

Key responsabilities:

Support monthly and quarterly Quality metrics reporting

Perform batch record review and product dispositions

Evaluate compliance of manufacturing records

Liaise with Regulatory Affairs on process changes

Assist in the preparation of Annual Product Quality Report

Job description

Description

Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medicines that meet significant unmet medical needs. Ardelyx has two commercial products approved in the United States, IBSRELA® (tenapanor) and XPHOZAH® (tenapanor). Ardelyx has agreements for the development and commercialization of tenapanor outside of the U.S. Kyowa Kirin commercializes PHOZEVEL® (tenapanor) for hyperphosphatemia in Japan. A New Drug Application for tenapanor for hyperphosphatemia has been submitted in China with Fosun Pharma. Knight Therapeutics commercializes IBSRELA in Canada.

Purpose of the role

The QA Specialist III / IV will provide QA support for Quality Operations. Working in a fast-paced pharmaceutical environment with a broad scope of responsibilities, the candidate will be able to bring many different skills to the job, with a focus on QA activities. The position requires diverse skill sets and will provide the opportunity to challenge an individual’s abilities to carry out the assigned responsibilities. In addition, the position requires the candidate to possess strong document and quality risk assessment management experience, in a GxP environment.

Position Responsibilities

Support the reporting of Quality metrics on a monthly, and quarterly basis in support of Management reviews and KPI
Support various quality risk management frameworks
Perform batch record review and product dispositions in support of clinical trials, registration, validation, and commercial product distribution
Evaluate compliance of completed manufacturing records (batch records, COC/ COA, and any related data as applicable) from CMO as necessary to ensure that they are accurate and complete
Maintain Continued Process Verification data collection in real-time at batch release
Review all the supporting documents regarding Quality System documentation including deviations, OOS, product complaints, CAPAs, and document /change controls-related processes
Evaluate document changes for compliance requirements (SOPs, Master Batch records, etc.)
Support the analysis and reporting of product and process quality trends, and quality system performance against internal and external guidelines, standards, and regulations
Support QA CMO oversight activities to ensure required quality standards are maintained
Liaise with Regulatory Affairs on any manufacturing process changes that may impact regulatory filings
Collaborate with CMC to continually improve compliance with quality systems, internal SOPs, and regulatory requirements and to resolve minor and major deviations
Support Product complaint-handling activities.
Support the Annual Product Quality Report preparation
Support cGMP compliance audits of GMP suppliers’ quality systems
Support and conduct training for employees, as necessary
Perform other related duties as assigned from time to time-based on company needs

Position Requirements

Bachelor’s degree in science or equivalent relevant experience
7+ years of combined GxP experience in drug substance and drug product manufacturing process development, commercial manufacturing, analytical development, and/or quality control experience in biotechnology or pharmaceutical industries
Experience in a manufacturing setting as a Quality person in the plant (QA PIP)
Working knowledge and/or understanding of quality risk assessment management principles
Extensive knowledge of GMP regulations and guidance (such as US, EU, and ICH)
Extensive experience with Quality Assurance systems and processes
Effective organization and planning skills
Demonstrated ability to deal with frequent changes, delays, or unexpected events
Strong technical writing skills
Advanced software skills (including SharePoint, Visio, Project, Acrobat Pro, and Veeva (a plus)) and demonstrated troubleshooting and problem-solving techniques
Strategic planning, leadership, and negotiation skills, and the ability to develop and present training materials to large groups
Proven ability to work independently and under tight deadlines and pressure in a composed manner
Effective interpersonal and communication skills
Comfortable communicating with all levels of staff, including executives
Strong team player

Location

Remote

The anticipated annualized base pay range for this full-time position is $116,393 - $142,259. Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.

Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.

Ardelyx is an equal opportunity employer.

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