Senior Quality Assurance Associate
San Diego, CA, US
Scientific
Bachelors Degree
Full Time, Temporary
$52.00/HR
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
San Diego, CA, US
$52.00/HR
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Job Title: Senior Quality Assurance Associate
Location: San Diego, CA- ONSITE
Duration: 3 months and may lead to temp to hire
Pay: $52.00/HR
Shift: MON-FRI 8AM – 4:30PM
Requirements:
• Bachelors or Master’s degree in a scientific discipline or relevant equivalent knowledge and experience
• 10+ years Quality Assurance experience in a GMP manufacturing environment or equivalent experience
• Six Sigma or ASQ certification preferred
Knowledge/Skills Requirements:
• Use existing procedures and established literature to solve routine and non-routine problems
• Utilize all elements of the quality system to identify, classify and control the status of finished products produced
• Based on broad technical skills and QA experience, anticipates and identifies unmet customer needs
• Proactive to address work issues at the individual, team and department level
• Ability to follow and provide a variety of instructions furnished in written, oral, diagram or schedule form
• Ability to identify and provide guidance/mitigation for aberrant data and potential quality/compliance concerns escalating to management
• Lead by example according to Catalent’s values and culture
• Able to lead difficult discussions with customers and drive them to an acceptable resolution
• Provides reliable/defendable interpretations of regulatory guidance for the customer and is capable of defending these positions to regulatory agencies
• Ability to collaborate with peers and demonstrate leadership capabilities in a matrix environment.
The San Diego Clinical and Specialty Services (CSS) Quality Assurance Senior Specialist supports clinical trial projects, ensuring all work is performed in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs). The Senior Specialist provides regulatory expertise to the investigation and deviation management process. Participates in and maintains site audit readiness by working closely with all departments within the business unit. They ensure that testing methods are validated, equipment is calibrated, and results are accurate and reliable.
• Ensures that products are manufactured, packaged, tested and released
• Performs document generation and review
• Participates in CI projects with risk-based approach
• Ensures that products are manufactured, packaged, tested and released according to applicable procedures
• Perform product release applicable procedures
• Lead investigator for deviations and complaints
• Performs document generation and review
• Participates in CI projects with risk-based approach
• Support functions associated with the packaging of clinical and commercial drug material
• Perform batch record review
• Participates in CI projects with risk-based approach
• Lead investigator for deviations and complaints
• Performs in-process audits, line clearance, verification of line clearance.
• Performs shipment verification
• Assesses incoming damaged material
• Participate in document generation and review
• Performs annual retain inspections
• Lead investigator for deviations and complaints
• Participates in CI projects with risk-based approach
• Reviews/approves model protocol, randomizations
• Performs label approval, print requests, label release
• Participates in document generation and review
• Lead investigator for deviations and complaints
• Tracks metrics for label control.
• Participates in CI projects with risk-based approach
• Reviews and tracks investigations/ deviations and corrective actions
• Participating in reported incidents to support quality compliance and business needs
• Assist in data compilation and management support of client business and quality review meetings
• Participates in CI projects with risk-based approach
Why Kelly?
Kelly® puts you in charge of your career, with access to cutting edge projects and technologies in industry leading organizations. Top companies throughout the world have trusted Kelly as a premier source of engineering & scientific talent and services since 1965. And Engineering & Scientific job seekers know Kelly® as a firm with an unmatched reputation for quality, integrity and professionalism. Whether you seek the variety and flexibility of working on short-term project engagements or prefer contract-to-hire or direct hire placement with our clients, apply with Kelly® to explore opportunities that suit your specific professional interests.
As a Kelly Services employee, you will have access to numerous perks, including:
- Exposure to a variety of career opportunities as a result of our expansive network of client companies
- Career guides, information and tools to help you successfully position yourself throughout every stage of your career
- Access to more than 3,000 online training courses through our Kelly Learning Center
- Weekly pay and service bonus plans
- Group-rate insurance options available immediately upon hire*
10163915
I want more jobs like this in my inbox.
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.