A QC Specialist is needed for a Swiss multinational manufacturing company for the pharmaceutical, biotechnology and nutrition sectors, in the Vacaville, CA area. The QC Specialist is responsible for supporting the planning, management, and execution of projects related to the product portfolio within a Quality Control organization, ensuring compliance with GMP standards while collaborating with internal and external partners.
location: Vacaville, California
job type: Contract
salary: $23.33 - 31.04 per hour
work hours: 8am to 5pm
education: Bachelors
responsibilities:
- Assist with projects and simple to complex technical activities associated with method improvements, method transfers, and possibly lab related activities.
- Work with internal departments, collaborators and partners concerning projects and commitments.
- Support coordination with customers to support multi-site operational activities.
- Assure and apply GMP throughout operations.
- Participate in group and project teamwork activities; project and process improvements.
- Assist in execution of projects such as method transfers, and method validations.
- Support simple to complex technical activities associated with products, control systems, health authority filings.
- Support methods monitoring and reference material replenishment and testing.
- Identify discrepancies, as applicable.
- Knowledge of GMP quality control pharmaceutical systems strongly desired. ·
- strong skills in detailed planning with cross-functional teams ·
- Ability to negotiate, influence, and make decisions in order to meet local, network, and global objectives and initiatives. ·
- strong verbal and written communication skills, ability to organize and present information both formally and informally. ·
- Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in multiple analytical and/or biological test procedures. ·
- Routinely exercises sound judgment, reasoning and problem solving. ·
- Capable of working with moderate independence or under moderate supervision and planning priorities and supporting potentially multiple projects and teams.
- Requires a BS/BA degree, preferably in a scientific discipline and
- 2-3 years of experience in commercial quality control within the pharmaceutical or biopharmaceutical industry.
qualifications:
- Experience level: Experienced
- Education: Bachelors
skills:
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.
