Top 41 Qa document control Jobs in San Diego, Ca

QA Associate III
PCI Pharma Services —San Diego, CA
- $29.65 - $33.36 an hour
- Full-time
- ERP systems
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
QA Specialist I
PCI Pharma Services —San Diego, CA
- $29.65 - $33.36 an hour
- Full-time
- High school diploma or GED
- Bachelor's degree
- Continuous improvement
- Health insurance
- Dental insurance
Clinical - QA Associate, Clinical Studies
Medvacon Life Sciences, LLC —San Diego, CA
- $33 an hour
- 8 hour shift
- Mid-level
- Math
- Associate's degree
QA Associate III - Second Shift (2-10)
PCI Pharma Services —San Diego, CA
- $29.65 - $33.36 an hour
- Full-time
- ERP systems
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
QA Specialist
Abzena Inc. —San Diego, CA
- $90,000 - $125,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
Quick Apply
Quality Control Associate
SMSbiotech, Inc —San Diego, CA
- $60,000 - $68,000 a year
- Full-time
- Data analysis skills
- Mid-level
- Driver's License
- Mileage reimbursement
- Health insurance
Quick Apply
QA Associate I - Second Shift (2-10)
PCI Pharma Services —San Diego, CA
- $21.69 - $24.41 an hour
- Full-time
- Laboratory experience
- High school diploma or GED
- Bachelor's degree
- Health insurance
- Dental insurance
QA Associate I
PCI Pharma Services —San Diego, CA
- $21.69 - $24.41 an hour
- Full-time
- Laboratory experience
- High school diploma or GED
- Bachelor's degree
- Health insurance
- Dental insurance
11h
Quality Control Associate, Raw Materials
Capricor Therapeutics —San Diego, CA
- $70,000 - $87,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
- Paid parental leave
- AD&D insurance
Quick Apply
Data Entry & QMS Data Migration Specialist (Structured Data & System Implementation)
Biolegacy Research —San Diego, CA
- $25 - $27 an hour
- Office
- High school diploma or GED
- SQL
Quick Apply
Quality Assurance Specialist
Siemens Healthineers —San Diego, CA
- $89,220 - $122,672 a year
- Full-time
- Microsoft Outlook
- Inventory management
- Writing skills
- Disability insurance
- Health insurance
Quality Associate, Batch Record Review and Product Disposition
Travere Therapeutics —San Diego, CA
- $85,000 - $105,000 a year
- Online Application
- Laboratory experience
- Mid-level
- Continuous improvement
- Health insurance
- Paid time off
Quality Control Inspector
IMIA, LLC —San Diego, CA
- $30 - $38 an hour
- Overtime
- Word processing
- Computer literacy
- Mid-level
- On-the-job training
Quick Apply
Quality Specialist 3
Grifols —San Diego, CA
- $97,000 - $115,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor of Science
- Paid holidays
- Health insurance
7d
Quality System Specialist (Veeva eQMS Specialist)
Viking Therapeutics, Inc. —San Diego, CA
- $95,000 - $115,000 a year
- System design
- Mid-level
- 3 years
Quick Apply
14d
QA Operations Specialist II
Maravai LifeSciences —San Diego, CA
- $60,000 - $70,000 a year
- 5 years
- Mid-level
- Analysis skills
- Health savings account
- Paid holidays
10d
Software Test Analyst 2
Cellanome —San Diego, CA
- $75,000 - $90,000 a year
- Computer Science
- Data analysis skills
- No experience needed
- Health insurance
- 401(k)
3d
QA Group Lead - Second Shift (2-10)
PCI Pharma Services —San Diego, CA
- $36.54 - $41.10 an hour
- Full-time
- Mid-level
- Bachelor's degree
- 1 year
- Health insurance
- Dental insurance
Manager, Clinical Quality System Documents
Arrowhead Pharmaceuticals —San Diego, CA
- $120,000 - $145,000 a year
- Microsoft Word
- 5 years
- Bachelor of Science
13d
QC Technologist III
Werfen —San Diego, CA
- $34 - $39 an hour
- Online Application
- ERP systems
- Data analysis skills
- Maintenance
12d

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QA Associate III

PCI Pharma Services -
San Diego, CA

Apply Now

Job Details

Full-time
$29.65 - $33.36 an hour

Benefits

Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Vision insurance

Qualifications

High school diploma or GED
Manufacturing facility experience
Quality assurance experience within pharmaceutical industry
Productivity software
Pharmaceutical manufacturing facility experience

Full Job Description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

This position performs a range of routine and semi-routine QA Raw Materials activities to ensure compliance with Quality Assurance and regulatory requirements. Responsibilities include supporting audits, training programs, and documentation review for GMP operations. The role promotes a compliant cGMP environment by following SOPs and provides quality support for investigations related to GMP manufacturing events. It also generates and reviews documentation for batch disposition and batch record assembly. The individual can work independently, within guidelines, and as part of a team. Additional duties include leading projects and training junior staff.

ESSENTIAL JOB FUNCTIONS-OTHER DUTIES MAY BE ASSIGNED:

Assists in regular follow ups with end users to ensure timely completion of open investigations and investigation activities.
Assist in ensuring the adequacy of investigations performed in relation to manufactured drug product and drug substance to support the batch release process.
Provides quality support in the review and approval of quality reports including deviations, OOSs, complaints, OOTIs, SCARs, and corrective and preventive actions (CAPAs)
Generates and compiles lot file review documentation for batch disposition.
Updates lot status in ERP system.
Responsible for equipment inductions, revisions and record maintenance within the electronic database.
Performs Technical Quality review of validation protocols and reports.
Performs logbook documentation audits for cGMP regulated logs and SOPs.
Creates, revises and approves procedures.
Performs the review of equipment and facility related Change Control documentation.
Assists with internal, client and regulatory audits.
Assists with the generation of department metrics.
Assists with developing recommendations for continuous improvement projects.
Assists in the review and approval of production batch records and associated data for product disposition.
Assists in the review and approval of controlled documents including standard operating procedures, protocols, and reports.
Regular and reliable attendance on a full-time basis [or in accordance with posted schedule].
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Fosters a safe and environmentally sustainable workplace by following all PCI EHS policies and procedures.
Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and company culture.

EDUCATION AND EXPERIENCE:

High School Diploma or equivalent. Bachelor’s degree strongly preferred in a Life Sciences discipline or equivalent.
Minimum of three to five (3-5) years of relevant GMP experience in documentation, QA on the floor, manufacturing, or equivalent.
Knowledge of cGMP regulations and good documentation practices preferred.
Strong organizational and analytical skills.
Must be familiar with Microsoft Office applications.

The hiring rate for this position is $29.65 - $33.36/hour plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), flexible spending account, and 401(k).

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Apply Now

Refine Your Search

qa document control jobs in san diego, ca

QA Associate III

QA Specialist I

Clinical - QA Associate, Clinical Studies

QA Associate III - Second Shift (2-10)

QA Specialist

Quality Control Associate

QA Associate I - Second Shift (2-10)

QA Associate I

Quality Control Associate, Raw Materials

Data Entry & QMS Data Migration Specialist (Structured Data & System Implementation)

Quality Assurance Specialist

Quality Associate, Batch Record Review and Product Disposition

Quality Control Inspector

Quality Specialist 3

Quality System Specialist (Veeva eQMS Specialist)

QA Operations Specialist II

Software Test Analyst 2

QA Group Lead - Second Shift (2-10)

Manager, Clinical Quality System Documents

QC Technologist III

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