Sr. Quality Analyst
Date Posted : 2012-04-06
Group : Science Biotech Jobs
Are you someone who realy wants to make a difference in the world?
Join our passionate team and spend your day helping people
change their lives and acheive their dreams!
California Cryobank (www.cryobank.com), one of the largest and most respected reproductive tissue banks in the industry, provides anonymous donor semen services as well as private storage of semen, eggs and embryos to thousands of people around the world each year. Our subsidiary division, FamilyCord (www.familycord.com) is a top-tier umbilical cord blood processing and storage company recognized as a leader and innovator within the rapidly growing cord blood banking industry.
California Cryobank is privately-held, with headquarters in West Los Angeles and branches in Westwood, Palo Alto, Boston and New York City. We have built a reputation of quality and caring for over 33 years and are poised for continued growth and success.
We have an immediate opening for a Sr. Quality Analyst to provide quality control and assurance support in our Corporate Headquarters in W. Los Angeles. Primary duties include:
independantly manages the CAPA system including organizing meetings with other department managers to conduct investigations, corrective action, preventive action plan and follow-up.
Manages client complaints using CAPA system.
Monitors Quality Control of the CCB product processing on a monthly basis, maintains the data of non-conformances, generate reports, and informs Quality Supervisor or Director about any important events or developments requiring immediate attention.
Reviews and analyses trend analytical data as needed to draft reports for senior management.
Organizes meetings, agendas, and generates meeting minutes for internal quality departmental meetings and companywide quarterly quality meetings.
Participates in and supports companywide audits and inspections.
Provides support to Quality Supervisor to manage Document Control and companywide licensing.
Supports Compliance Manager in order to manage companywide Safety Program by conducting regular safety inspections and training.
Writes and maintains quality and regulatory procedures.
Communicates effectively with internal staff, company-wide departments and CCB clients.
Supports department by providing CCB staff training on Quality System requirements.
Other job duties or projects as assigned.
Bachelor of Science Degree and 3-4 years Quality/Regulatory experience and/or training in the Biotechnology industry, including drafting quality and regulatory procedures/reports
familarity with regulatory compliance issues and laboratory (blood bank)/medical terminology.
MS Office skills
Superb written, verbal and interpersonal skills
Excellent organizational, prioritization and time management skills
Personable, professional demeanor and ability to interact with regulatory bodies
Ability to work effectively in both independantly and in a team enviroment
High attention to detail, follow-through, and accuracy
Ability to handle multiple concurrent activities and competing priorities
Ability to handle highly sensitive and confidential infomation with integrity
We offer competitive compensation and benefits, inc.:
Group health, dental and vision insurance
Company-paid Life and Disability Insurance
Health Care and Dependent Care Flexible Spending Accounts
Generous Paid Time Off (PTO) policy (19 days to start!)
Please submit your cover letter with salary requirements and resume to:
Attn: Sr. Quality Analyst
No phone calls please. EOE