About this role
Sr. Quality Control (QC) Specialist
Pay: $50 - $53.96 per hour
Duration: 5 months
Location: Onsite (initially in Santa Monica for the month of November, some remote time, then return to office in Thousand Oaks)
Responsibilities (include but not limited to):
- Execute global reporting control and invalid trending programs.
- Execute data extraction from LIMs system to support reporting requirements.
- Lead/coordinate continuous improvement activities partnering with sites.
- Author Annual Product Review Laboratory Section.
- Author technical quarterly invalid and biannual control trending reports.
- Interact with the laboratory operations group to support new methods, technology, and KLIMS implementation and ongoing support for new module implementations and/or installation of new capabilities.
- Meet reporting deadlines as defined per procedure demonstrating organizational, prioritization, and time management proficiencies.
- Highly effective written and oral communication skills to address a cross-functional audience.
- Self-motivated, detail-oriented, and willingness to support other team members.
- Improve processes to minimize complexities and optimize operational effectiveness.
- Proficient with statistical tools such as JMP and/or Minitab.
- Proficient in Microsoft Office application.
- Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/210/211), Quality Control, GMPs, GLP.
Basic Qualifications:
- Master's Degree and 4+ years' experience in a Quality function in the pharmaceutical or biotechnology industry
- OR Bachelor's Degree and 6+ years' experience in a Quality function in the pharmaceutical or biotechnology industry
- OR High School Degree and 10+ years' experience in a Quality function in the pharmaceutical or biotechnology industry.
Preferred Qualifications:
- Experience with gene and cell therapies or pharmaceutical industry, Statistical knowledge in biologics is a plus.
- Able to adjust workload based upon changing priorities.
- Experience in Risk Management processes a plus.
- Experience with US and international health authority inspections a plus.
EEO Statement
The staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process, and always double check the email address of the Recruiter to ensure it’s from an official Planet domain (@theplanetgroup.com or @launchcg.com) - and not a domain with an alternative extension like .net, .org, or .jobs.
The Planet Group and our companies are equal opportunity employers. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity, and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.
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About The Planet Group
The Planet Group is a global professional services firm delivering strategic staffing and advisory solutions. We operate at the intersection of talent and transformation – connecting the right people with the right opportunities in the areas of technology, engineering, accounting & finance, digital marketing, and manufacturing.
As one of the largest staffing companies in the US, we operate with a global reach and a performance-first mindset. We partner with clients to move fast, stay agile, and drive measurable results – building high-impact teams that fuel transformation and growth.