-
Quality Assurance Auditor
3 weeks ago
Altasciences Cypress, United StatesYour New Company · At Altasciences we all · move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.No matter your role, we all play an important part and you will have a significant impa ...
-
Senior IT Auditor, IS Assurance
3 days ago
BDO Costa Mesa, United States Full timeJob Summary: · The Assurance Senior, IS Assurance is responsible for assisting in the planning of the IT audit engagement and executing the IT risk assessment and control evaluation to determine impact of controls on financial audit procedures. In this role, the Assurance Senior ...
-
Quality Assurance Auditor
3 weeks ago
Patco Brands Los Angeles, United StatesPatco Brands is one of the fastest growing beverage companies in the United States. Independently owned, Patco has established itself by using 100% Blue Weber Agave and a proprietary process to innovate within the fast growing ready-to-drink spirits category. · Patco is a maker ...
-
GMP Quality Assurance Auditor
3 weeks ago
SciPro Inc. Los Angeles, United States FreelanceWe are looking for an experienced QA Auditor, to audit suppliers and CDMO's for a CAR-T Biotech client in California. This role will be to support a few small audits, however, we are looking for someone that has capacity to work with a number of other clients as we are seeing a d ...
-
Quality Assurance Auditor
3 weeks ago
Patco Brands Los Angeles, United StatesPatco Brands is one of the fastest growing beverage companies in the United States. Independently owned, Patco has established itself by using 100% Blue Weber Agave and a proprietary process to innovate within the fast growing ready-to-drink spirits category. · Patco is a maker ...
-
Quality Assurance Auditor
3 weeks ago
24 Seven Talent Los Angeles, United StatesOur beverage client is looking to bring on a Quality Assurance Auditor to their team on a fulltime basis, sitting in California or on the West Coast as this role will require travel. · Responsibilities: · Travel to all production and co-manufacturing facilities on a regular bas ...
-
Quality Assurance Auditor
3 weeks ago
24 Seven Talent Los Angeles, United StatesOur beverage client is looking to bring on a Quality Assurance Auditor to their team on a fulltime basis, sitting in California or on the West Coast as this role will require travel. · Responsibilities: · Travel to all production and co-manufacturing facilities on a regular basi ...
-
Manager, Clinical Quality Assurance Auditor
3 weeks ago
Arrowhead Pharmaceuticals Pasadena, United StatesJob Description · Job DescriptionArrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient m ...
-
Sr Auditor, Clinical Quality Assurance
3 weeks ago
MicroVention Aliso Viejo, United StatesProvide support to all aspects of the Clinical Quality Assurance (CQA) function across the business. Support CQA Management in assuring quality throughout MicroVention and promote continual improvement processes to ensure all systems and procedures are compliant with Standard Ope ...
-
Sr Auditor, Clinical Quality Assurance
3 weeks ago
MicroVention Aliso Viejo, United StatesProvide support to all aspects of the Clinical Quality Assurance (CQA) function across the business. Support CQA Management in assuring quality throughout MicroVention and promote continual improvement processes to ensure all systems and procedures are compliant with Standard Ope ...
-
Manufacturing Quality Assurance Auditor
3 weeks ago
Spectraforce Technologies Los Angeles, United StatesPosition Title: · Manufacturing Quality Assurance Auditor · Location: · Woodland, CA · Duration: · 7 Months · Job Description: · Support a wide array of quality department tasks relating to developing and implement systems, procedures, and projects required to successfully ...
-
Ernst & Young Irvine, United StatesEY focuses on high-ethical standards and integrity among its employees and expects all candidates to demonstrate these qualities. At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the b ...
-
EY - Ernst & Young Global Limited Irvine, United StatesEY focuses on high-ethical standards and integrity among its employees and expects all candidates to demonstrate these qualities. At EY, youll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture Audit, Auditor, Accounting, Ser ...
-
Sr Auditor, Clinical Quality Assurance
3 weeks ago
MicroVention Aliso Viejo, United States12071BR · Title: · Sr Auditor, Clinical Quality Assurance · Job Description: · Provide support to all aspects of the Clinical Quality Assurance (CQA) function across the business. Support CQA Management in assuring quality throughout MicroVention and promote continual improve ...
-
EY Irvine, United States Paid WorkEY focuses on high-ethical standards and integrity among its employees and expects all candidates to demonstrate these qualities. At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the b ...
-
Ernst & Young Los Angeles, United StatesJob Description · EY focuses on high-ethical standards and integrity among its employees and expects all candidates to demonstrate these qualities. At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technolo ...
-
EY Los Angeles, CA, United StatesEY focuses on high-ethical standards and integrity among its employees and expects all candidates to demonstrate these qualities. At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the b ...
-
Sr. Supplier Quality Engineer
1 week ago
iRhythm Technologies Cypress, United StatesBoldly innovating to create trusted solutions that detect, predict, and prevent disease. · Discover your power to innovate while making a difference in patients' lives. iRhythm is advancing cardiac care...Join Us Now · At iRhythm, we are dedicated, self-motivated, and driven to ...
-
Sr. Supplier Quality Engineer
1 week ago
iRhythm Technologies Cypress, United StatesBoldly innovating to create trusted solutions that detect, predict, and prevent disease. · Discover your power to innovate while making a difference in patients' lives. iRhythm is advancing cardiac care...Join Us Now · At iRhythm, we are dedicated, self-motivated, and driven to ...
-
Health Center Supervisor
5 days ago
Planned Parenthood Los Angeles Lakewood, United StatesPlanned Parenthood Los Angeles is seeking an experienced and caring · Health Center Supervisor · with excellent communication and customer service skills to join our talented team at our Long Beach Central Health Center. This is not a desk job. · PPLA managers roll up their sl ...
Quality Assurance Auditor - Cypress, United States - Altasciences
Description
Your New CompanyAt Altasciences we all
move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.
No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe.
By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team Whether youre a recent college graduate or seeking your next career opportunity, its time to discover your future at Altasciences.
We are better together and together We Are Altasciences.About the role
The QA Auditor reports to the QA Manager and is responsible for carrying out systematic and independent examination (i.e., audit) of multiple clinical trial-related activities and documents, to determine whether the activities were conducted, and the data were recorded, analyzed, and accurately reported according to the protocol, standard operating procedures (SOPs) and Good Clinical Practices.
They are responsible for reporting any findings to the Internal Study Team and department management (e.g., Team Manager, Study Manager, Director, etc.) and for building and maintaining effective working relationships throughout the organization.
What You'll Do HereAudits phases of laboratory and clinical studies, reports, and performs related duties (e.g., issues findings and QA statements) to ensure regulatory compliance.
Audits all disciplines (examples of disciplines include Screening, Recruiting, Clinical Operations, Laboratory, Data Services).Performs in-life audits, process audits, vendor qualifications, equipment and software validation audits.
Writes and issues inspection reports. Works with internal clients to ensure that inspection findings are clearly communicated and understood. Evaluates inspection finding responses to ensure they are written to address the findings appropriately.
Ensures through phase and data inspections that the SOPs, which are involved in the conduct of a study, are current and practiced.
Identifies and communicates opportunities for process improvement based on audit and inspection observations.Participates in and guides process improvement activities in both small intradepartmental groups as well as complex and possible multidepartment interactions.
Maintains necessary documentation of QA records and study files.Notifies management of observed quality and compliance trends in the areas inspected.
Under supervision of a mentor/coach, performs the following tasks: SOP QA review, client hosting, regulatory agency hosting and external test site/clinical site/bioanalytical laboratory qualifications.
Recommends modifications in procedures to fit special needs or problems and involves manager when assistance in process improvement/resolution is necessary.
Interprets GCP, GLP, and GCLP and associated regulatory documents to facilitate auditing and process improvement recommendations.Prepares for RQAP-GCP and/or RQAP-GLP certification.
Carries out appropriate self-development efforts as directed.
What You'll Need to Succeed
Bachelor degree or higher, in Chemistry, Biochemistry, Biology, or equivalent field, or equivalent combination of education and experience, in the pharmaceutical industry
Two to three years related technical experience and/or training. A minimum of two years auditing.
Professional certification such as RQAP-GLP (Registered Quality Assurance Professional-GLP) or ASQ-CQA (American Society of Quality Certified Quality Auditor) or other certification is recommended
What We Offer
The pay range estimated for this position is $67,500 to $85,000 per year.
Please note that salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.
May consider Senior level Auditors as well.Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes:
Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & TelehealthPrograms
Training & Development Programs
Employee Referral Bonus Program
#LI-AN1
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion.
Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives.
All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation.
Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences#J-18808-Ljbffr
