Poseida Therapeutics, Inc.
Manufacturing Quality Assurance Associate
Poseida Therapeutics, Inc., San Diego, California, United States, 92189
Manufacturing Quality Assurance Associate
Join to apply for the
Manufacturing Quality Assurance Associate
role at
Poseida Therapeutics, Inc.
This range is provided by Poseida Therapeutics, Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range:
$27.13/hr - $50.38/hr
Your Impact:
You will be an integral part of a friendly Quality Assurance Team that is dedicated, agile, and collaborative. In this role, you will work on-site directly with all GMP‑related functional teams that are committed to delivering quality products to our clinical patients. Your talents and expertise will directly contribute to the passion to develop innovative therapies with the capacity to cure. You will learn and advance in your career as this group is forward‑thinking and fully supportive of career development. If you are an individual that is driven to make a difference, have a strong work ethic, and want to be part of an exciting bigger picture, the Quality Assurance team welcomes you!
Position Summary:
We are seeking an exceptional candidate to join our Quality team in San Diego, CA. The Manufacturing Quality Assurance Associate candidate will have Manufacturing Quality Assurance (MQA) related responsibilities to ensure Poseida’s starting materials and clinical products meet cGMP requirements. This role reports to the Senior Quality Assurance Specialist.
Responsibilities include but are not limited to:
Effectively communicate and collaborate with internal Quality Assurance, Manufacturing, Quality Control, Procurement, and Facilities teams
Review executed production batch records and associated testing data to ensure the records meet cGMP expectations
Participate in QA team meetings
Supports the use of and maintains Quality trackers as assigned
Participate in the creation, revision, and review of basic SOPs, Forms, Work Instructions and other controlled documents within the QMS, as requested
Qualify for and perform clean‑room (ISO classified) gowning for all QA on‑the‑floor support activities for internal manufacturing processes
Perform QA line clearance activities
Perform duties related to the raw material program, and other MQA support activities as assigned
Identify opportunities for improvement within the assigned roles and responsibilities and take initiative to communicate and drive positive change
Complete other Quality Assurance based activities as assigned
Align daily actions with department goals and company culture
Drive the spirit of teamwork across all functions by supporting a team approach with focus on our patients being the top priority
Fosters and embraces an environment of teamwork, accountability and responsibility that supports the manufacture of a quality product
Requirements, Knowledge, Skills and Abilities:
A minimum of a Bachelor’s degree in life sciences or a related field with a minimum of 2 years of relevant experience; GMP/GxP experience preferred (an equivalent combination of education and experience may be considered)
Knowledge of cGMP, FDA, ICH and EU regulations
Controlled document review and /or batch release experience preferred
Basic understanding of Deviations, CAPAs and Change Control processes
Detail oriented with strong written and verbal communication skills
Basic computer skills in Excel, PowerPoint, and Word processing
Ability to work independently, within prescribed guidelines, and as a team member
Demonstrated ability to work effectively in a dynamic, complex and fast‑paced team environment
Ability to support a flexible work schedule to accommodate the Manufacturing schedule
Must be able to achieve and retain cleanroom (ISO classified) gowning qualified status
Must be physically capable to lift 20 pounds and stand for periods up to 2 hours
Manufacturing Quality Assurance Associate Pay Rate: $27.13/hour to $50.38/hour
The final pay offered to a successful candidate 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 with the industry, education, geographic location, etc.
Who We Are and What We Do Poseida Therapeutics was acquired by Roche in early 2025 and is now part of the Roche Group. Poseida is a clinical‑stage biopharmaceutical company advancing differentiated allogeneic cell therapies and genetic medicines with the capacity to cure. The Company’s approach is based on its proprietary genetic editing platforms, including its non‑viral DNA Delivery System, Cas‑CLOVER™ Site‑Specific Gene Editing System, Booster Molecule and nanoparticle gene delivery technologies, as well as in‑house GMP cell therapy manufacturing.
Our people are as important as our cutting‑edge technology. That’s why we invest in offering excellent career development opportunities to our employees, as well as highly competitive compensation and comprehensive benefits. We are committed to giving employees the resources they need to thrive, personally and professionally.
Recruitment Fraud Alert Alert: Beware of Employment Scams
Poseida Therapeutics, Inc. has received reports of employment‑related scams. These scams have appeared in forms of false job advertisements and/or unsolicited contacts via communication/chat platforms, phone, email or text from individuals claiming to be or represent Poseida’s Human Resources team. Be advised that Poseida Therapeutics does not extend unsolicited employment offers. Furthermore, Poseida Therapeutics does not request payment information or charge prospective employees with any fees during the recruitment process.
If you would like to pursue employment opportunities with Poseida Therapeutics, Inc., please visit our official careers website https://poseida.com/careers-culture/ or official Poseida Therapeutics LinkedIn page. Job postings that do not link directly to our careers website or official Poseida LinkedIn page are not legitimate and might be fraudulent. You may report fraudulent job advertisements or contacts via our Contact Us page at https://poseida.com/contact-us/ and select the subject “Careers.” If you have been defrauded or suspect identity theft as a result of an employment scam, please contact your local law enforcement agency for guidance.
Seniority level
Associate
Employment type
Full‑time
Job function
Quality Assurance
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Manufacturing Quality Assurance Associate
role at
Poseida Therapeutics, Inc.
This range is provided by Poseida Therapeutics, Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range:
$27.13/hr - $50.38/hr
Your Impact:
You will be an integral part of a friendly Quality Assurance Team that is dedicated, agile, and collaborative. In this role, you will work on-site directly with all GMP‑related functional teams that are committed to delivering quality products to our clinical patients. Your talents and expertise will directly contribute to the passion to develop innovative therapies with the capacity to cure. You will learn and advance in your career as this group is forward‑thinking and fully supportive of career development. If you are an individual that is driven to make a difference, have a strong work ethic, and want to be part of an exciting bigger picture, the Quality Assurance team welcomes you!
Position Summary:
We are seeking an exceptional candidate to join our Quality team in San Diego, CA. The Manufacturing Quality Assurance Associate candidate will have Manufacturing Quality Assurance (MQA) related responsibilities to ensure Poseida’s starting materials and clinical products meet cGMP requirements. This role reports to the Senior Quality Assurance Specialist.
Responsibilities include but are not limited to:
Effectively communicate and collaborate with internal Quality Assurance, Manufacturing, Quality Control, Procurement, and Facilities teams
Review executed production batch records and associated testing data to ensure the records meet cGMP expectations
Participate in QA team meetings
Supports the use of and maintains Quality trackers as assigned
Participate in the creation, revision, and review of basic SOPs, Forms, Work Instructions and other controlled documents within the QMS, as requested
Qualify for and perform clean‑room (ISO classified) gowning for all QA on‑the‑floor support activities for internal manufacturing processes
Perform QA line clearance activities
Perform duties related to the raw material program, and other MQA support activities as assigned
Identify opportunities for improvement within the assigned roles and responsibilities and take initiative to communicate and drive positive change
Complete other Quality Assurance based activities as assigned
Align daily actions with department goals and company culture
Drive the spirit of teamwork across all functions by supporting a team approach with focus on our patients being the top priority
Fosters and embraces an environment of teamwork, accountability and responsibility that supports the manufacture of a quality product
Requirements, Knowledge, Skills and Abilities:
A minimum of a Bachelor’s degree in life sciences or a related field with a minimum of 2 years of relevant experience; GMP/GxP experience preferred (an equivalent combination of education and experience may be considered)
Knowledge of cGMP, FDA, ICH and EU regulations
Controlled document review and /or batch release experience preferred
Basic understanding of Deviations, CAPAs and Change Control processes
Detail oriented with strong written and verbal communication skills
Basic computer skills in Excel, PowerPoint, and Word processing
Ability to work independently, within prescribed guidelines, and as a team member
Demonstrated ability to work effectively in a dynamic, complex and fast‑paced team environment
Ability to support a flexible work schedule to accommodate the Manufacturing schedule
Must be able to achieve and retain cleanroom (ISO classified) gowning qualified status
Must be physically capable to lift 20 pounds and stand for periods up to 2 hours
Manufacturing Quality Assurance Associate Pay Rate: $27.13/hour to $50.38/hour
The final pay offered to a successful candidate 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 with the industry, education, geographic location, etc.
Who We Are and What We Do Poseida Therapeutics was acquired by Roche in early 2025 and is now part of the Roche Group. Poseida is a clinical‑stage biopharmaceutical company advancing differentiated allogeneic cell therapies and genetic medicines with the capacity to cure. The Company’s approach is based on its proprietary genetic editing platforms, including its non‑viral DNA Delivery System, Cas‑CLOVER™ Site‑Specific Gene Editing System, Booster Molecule and nanoparticle gene delivery technologies, as well as in‑house GMP cell therapy manufacturing.
Our people are as important as our cutting‑edge technology. That’s why we invest in offering excellent career development opportunities to our employees, as well as highly competitive compensation and comprehensive benefits. We are committed to giving employees the resources they need to thrive, personally and professionally.
Recruitment Fraud Alert Alert: Beware of Employment Scams
Poseida Therapeutics, Inc. has received reports of employment‑related scams. These scams have appeared in forms of false job advertisements and/or unsolicited contacts via communication/chat platforms, phone, email or text from individuals claiming to be or represent Poseida’s Human Resources team. Be advised that Poseida Therapeutics does not extend unsolicited employment offers. Furthermore, Poseida Therapeutics does not request payment information or charge prospective employees with any fees during the recruitment process.
If you would like to pursue employment opportunities with Poseida Therapeutics, Inc., please visit our official careers website https://poseida.com/careers-culture/ or official Poseida Therapeutics LinkedIn page. Job postings that do not link directly to our careers website or official Poseida LinkedIn page are not legitimate and might be fraudulent. You may report fraudulent job advertisements or contacts via our Contact Us page at https://poseida.com/contact-us/ and select the subject “Careers.” If you have been defrauded or suspect identity theft as a result of an employment scam, please contact your local law enforcement agency for guidance.
Seniority level
Associate
Employment type
Full‑time
Job function
Quality Assurance
Pharmaceutical Manufacturing
#J-18808-Ljbffr