QA Associate I, Manufacturing
$60K - $70K/yr
QA Associate I, Manufacturing Position Summary: * Work Schedule: Monday-Friday, core hours 8am-4:30pm * 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and ...
$60K - $70K/yr
QA Associate I, Manufacturing Position Summary: * Work Schedule: Monday-Friday, core hours 8am-4:30pm * 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and ...
$60K - $70K/yr
QA Associate I, Manufacturing Position Summary: * Work Schedule: Monday-Friday, core hours 8am-4:30pm * 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and ...
Carlsbad, CA · On-site +1
$70K - $102K/yr
MANAGER/ QA ASSOCIATE, GxP QUALITY SYSTEMS SUMMARY: Ionis is seeking a Manager / QA Associate, GxP Quality Systems, to support compliance across Ionis quality systems. This role is responsible for ...
Carlsbad, CA · On-site +1
$70K - $102K/yr
MANAGER/ QA ASSOCIATE, GxP QUALITY SYSTEMS SUMMARY: Ionis is seeking a Manager / QA Associate, GxP Quality Systems, to support compliance across Ionis quality systems. This role is responsible for ...
Carlsbad, CA · On-site +1
$70K - $102K/yr
MANAGER/ QA ASSOCIATE, GxP QUALITY SYSTEMS SUMMARY: Ionis is seeking a Manager / QA Associate, GxP Quality Systems, to support compliance across Ionis quality systems. This role is responsible for ...
Carlsbad, CA · On-site +1
$70K - $102K/yr
MANAGER/ QA ASSOCIATE, GxP QUALITY SYSTEMS SUMMARY: Ionis is seeking a Manager / QA Associate, GxP Quality Systems, to support compliance across Ionis quality systems. This role is responsible for ...
The QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which consists of QA Production Floor supports, and QA Product Release. 2nd Shift Hours: 2 PM - 10:30 PM Monday through ...
The QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which consists of QA Production Floor supports, and QA Product Release. 2nd Shift Hours: 2 PM - 10:30 PM Monday through ...
Sacramento, CA · On-site
In Process QA Specialist (Full Time) At Nivagen as an In Process QA Specialist you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing ...
Sacramento, CA · On-site
In Process QA Specialist (Full Time) At Nivagen as an In Process QA Specialist you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing ...
Sacramento, CA · On-site
In Process QA Specialist (Full Time) At Nivagen as an In Process QA Specialist you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing ...
Quick apply
Sacramento, CA · On-site
In Process QA Specialist (Full Time) At Nivagen as an In Process QA Specialist you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing ...
In Process QA Specialist (Full Time) At Nivagen as an In Process QA Specialist you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing ...
In Process QA Specialist (Full Time) At Nivagen as an In Process QA Specialist you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing ...
San Francisco, CA · On-site
$121K - $167K/yr
ABOUT THE ROLE We are seeking a QA Associate Manager to join our Growth Marketing Operations (GROMO) team. This role is ideal for someone with a strong background in marketing campaign testing and ...
San Francisco, CA · On-site
$121K - $167K/yr
ABOUT THE ROLE We are seeking a QA Associate Manager to join our Growth Marketing Operations (GROMO) team. This role is ideal for someone with a strong background in marketing campaign testing and ...
Los Angeles, CA · Hybrid
$67K - $95K/yr
We are looking for a Quality Control Senior Associate to join our QA function of the Sourcing team at Everlane. In this role, you will work with our products, factories, and internal team to identify ...
Los Angeles, CA · Hybrid
$67K - $95K/yr
We are looking for a Quality Control Senior Associate to join our QA function of the Sourcing team at Everlane. In this role, you will work with our products, factories, and internal team to identify ...
Ensure quality control and risk management throughout the audit lifecycle Minimum qualifications * 5+ years hands-on experience as Senior Assurance Associate or Early Manager at EY, PwC, Deloitte, or ...
Ensure quality control and risk management throughout the audit lifecycle Minimum qualifications * 5+ years hands-on experience as Senior Assurance Associate or Early Manager at EY, PwC, Deloitte, or ...
Del Rey, CA · On-site
$17 - $19/hr
We are hiring Quality Control and Quality Assurance Associates to help ensure products meet company quality, safety, and production standards throughout the busy pomegranate season. This is a great ...
New
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Del Rey, CA · On-site
$17 - $19/hr
We are hiring Quality Control and Quality Assurance Associates to help ensure products meet company quality, safety, and production standards throughout the busy pomegranate season. This is a great ...
New
Palmdale, CA · On-site
$70K/yr
Train, coach, and develop QA associates on quality procedures, standards, and best practices. * Review and maintain accurate QA documentation, reports, and records. * Investigate product quality ...
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Palmdale, CA · On-site
$70K/yr
Train, coach, and develop QA associates on quality procedures, standards, and best practices. * Review and maintain accurate QA documentation, reports, and records. * Investigate product quality ...
San Diego, CA · On-site
$33/hr
... QA Associate - Clinical Supplies v1.0 • Excellent written and verbal communications skills with internal and external customers, peers and managers • Lead by example according to our values and ...
San Diego, CA · On-site
$33/hr
... QA Associate - Clinical Supplies v1.0 • Excellent written and verbal communications skills with internal and external customers, peers and managers • Lead by example according to our values and ...
San Diego, CA · On-site
$33/hr
Ability to identify aberrant data and potential quality/compliance concerns escalating to management CSD-JD-QA Associate - Clinical Supplies v1.0 * Excellent written and verbal communications skills ...
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San Diego, CA · On-site
$33/hr
Ability to identify aberrant data and potential quality/compliance concerns escalating to management CSD-JD-QA Associate - Clinical Supplies v1.0 * Excellent written and verbal communications skills ...
First Shift The Sr. Quality Associate I Quality Assurance will primarily serve as a Quality Systems technical specialist as part of the QA NFF/NFB business unit. He/She will develop and implement ...
First Shift The Sr. Quality Associate I Quality Assurance will primarily serve as a Quality Systems technical specialist as part of the QA NFF/NFB business unit. He/She will develop and implement ...
The role manages a team of QA Associates and works cross-functionally to resolve quality events and maintain operational excellence. Role Specific Requirements * Ensure ongoing compliance with local ...
The role manages a team of QA Associates and works cross-functionally to resolve quality events and maintain operational excellence. Role Specific Requirements * Ensure ongoing compliance with local ...
Pomona, CA · On-site
$122K - $149K/yr
The role manages a team of QA Associates and works cross-functionally to resolve quality events and maintain operational excellence. Role Specific Requirements * Ensure ongoing compliance with local ...
Pomona, CA · On-site
$122K - $149K/yr
The role manages a team of QA Associates and works cross-functionally to resolve quality events and maintain operational excellence. Role Specific Requirements * Ensure ongoing compliance with local ...
Carlsbad, CA · On-site
$154.50 - $196.87/hr
Associate Director, Development Quality Assurance Job Category: Development - Ionis Requisition Number: IONIS004059 * Full-Time Locations Showing 1 location Headquartered in Carlsbad, California, and ...
Carlsbad, CA · On-site
$154.50 - $196.87/hr
Associate Director, Development Quality Assurance Job Category: Development - Ionis Requisition Number: IONIS004059 * Full-Time Locations Showing 1 location Headquartered in Carlsbad, California, and ...
Day Quality Associate II / Quality Associate III, QA Release Summary: The Quality Associate II/II provides routine technical support for various tasks (i.e. documentation, training, compliance ...
Day Quality Associate II / Quality Associate III, QA Release Summary: The Quality Associate II/II provides routine technical support for various tasks (i.e. documentation, training, compliance ...
Foster City, CA · Hybrid
$190K - $205K/yr
POSITION SUMMARY The Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum's clinical study programs as the GCP-QA representative on the study management team; managing activities ...
Foster City, CA · Hybrid
$190K - $205K/yr
POSITION SUMMARY The Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum's clinical study programs as the GCP-QA representative on the study management team; managing activities ...
$12.81 - $17.21
17% of jobs
$18.66 is the 25th percentile. Wages below this are outliers.
$17.21 - $21.61
24% of jobs
The median wage is $23.81 / hr.
$21.61 - $26.01
18% of jobs
$26.01 - $30.41
15% of jobs
$30.78 is the 75th percentile. Wages above this are outliers.
$30.41 - $34.81
10% of jobs
$34.81 - $39.21
8% of jobs
$39.21 - $43.61
5% of jobs
$43.61 - $48.01
3% of jobs
$48.01 - $52.41
0% of jobs
$52.41 - $56.81
0% of jobs
$56.81 - $61.21
0% of jobs
$12
$28
$61
The most popular types of Qa jobs in California are:
Cities in California with the most Qa Associate job openings:

$60K - $70K/yr
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 15 days ago
7.6
Based on 55 frontline employees who took The Breakroom Quiz
59th of 86 rated pharmaceutical
QA Associate I, Manufacturing
Position Summary:
Work Schedule: Monday-Friday, core hours 8am-4:30pm
100% on-site (San Diego)
Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Catalent's San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of our Catalent Spray Drying technologies with downstream roller compaction capabilities to support the needs of our client's most challenging compounds.
The Manufacturing Quality Assurance (MQA) Associate I is responsible for a wide variety of activities pertaining to supporting, maintaining, and assuring compliance with quality systems requirements and applicable regulatory requirements; to advance the development and manufacture of drug candidates. This will include documentation review and approval, dispositioning of product or its intermediates and supporting manufacturing operations.
The Role:
Reviews and dispositions production batch records for product release. Determines if records are compliant with internal and cGMP regulations.
Liaison between Manufacturing and QA for executed Batch Record Review and flow of documents.
Liaison between QA and client and effectively communicates with clients in regards to Executed Batch Records and review status.
Tracks status of Executed Batch Records and maintains established deadlines for completion of review and corrections.
Reviews and approves GMP product labels.
Support GMP manufacturing activities including release of GMP materials, shipment verification and performance of production audits in a Class 100,000 environment, maintenance of clinical trial material inventory logs.
Other duties as assigned.
The Candidate:
High school diploma required; BS/BA degree desirable
Work experience in a GXP manufacturing environment or similar is preferred.
Candidate must also be highly detail-oriented and organized, able to work both independently and as a team player with a positive attitude.
Pay:
The anticipated salary range for this role in California is $60,000 to $70,000 annually. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why you should join Catalent:
Awesome employee activities: Movie Day, Monthly Birthday Celebrations, Friday Bagel Breakfast, On-site Fitness Center with machines, Sponsored Sports Teams, and several other company-sponsored events that encourages positive employee comradery, which contributes to effectively building positive employee relationships, overall creating a positive work environment.
Environmentally friendly green initiatives with on-site practices as well as regularly participating in Beach Clean-up activities for community engagement.
Defined career path and annual performance review and feedback process. Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
Several Employee Resource Groups focusing on Diversity and Inclusion.
Competitive salary with bonus potential. Generous 401K match and Paid Time Off accrual. Medical, dental and vision benefits effective day one of employment.
152 hours of PTO + 10 paid holidays.
Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic.
Tuition Reimbursement - Let us help you finish your degree or earn a new one!
WellHub program to promote overall physical wellness.
Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Sourced by ZipRecruiter
Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.
Pharmaceutical product wholesalers
10,000+ Employees
Somerset, NJ, US
2007