Associate, Quality Assurance - raw materials and components in Thousand Oaks

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Job DescriptionJob Descriptionjob summary:

This position is responsible for sampling and inspection of raw materials and components and for performing Quality review of documentation for assigned functions (e.g. equipment and maintenance records). Duties will include the operation and maintenance of instruments and equipment associated with sampling, e.g., Toledo balance, drum lift, pallet jack, etc. Maneuvering of large drums required. Employees will also be responsible for the maintenance of training records, recording and computing data.

Schedule/Shift: 1st shift, Mon.-Fri. The role offers long-term (3-year) engagement with limited overtime.

location: Newbury Park, California
job type: Contract
salary: $25.00 - 30.36 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:

• General inspection of received shipments of raw materials, components, and labels.
• Sampling of chemical raw materials and preparation of sample shipments.
• Quality inspection and dimensional analysis for component and label batches.
• Review of GMP shipment paperwork.
• GMP controlled document review.
• Receiving operations oversight and consultation (Purposeful Presence on the Floor).
• Initiation of deviation records.

qualifications:

• Bachelors degree (BS) OR Associates degree (AS) and 4 years of directly related experience OR High school diploma / GED and 6 years of directly related experience
• Ability to lift 50+ pounds and pass a vision assessment for inspection work.
• Must be comfortable working with raw materials and components, though no lab work is required
• General understanding of aseptic techniques, cGMPs, gowning, sampling procedures and safety guidelines

Qualifications:

• Bachelors Degree in Science OR Associates Degree in Science and 2-3 years of experience in biotechnology/Pharma environment.
• Work as a team player and/or independently
• Multi-task and basic problem solving skills
• Excellent communication skills
• Time management
• Proficient computer skills (i.e. documentation systems, databases and spreadsheets).

#LI-DB1

skills: Quality Assurance, GMP (Good Manufacturing Practice), Good Manufacturing Practices (GMP), Quality Assurance (QA), Good Documentation Practices (GDP)

Equal Opportunity Employer: Race, Color, , , , Gender , , , 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.

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