Quality Control Associate
$45 per hourAs a QC Analyst II, you will support various activities within the QC department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, drug substance and final product samples and other samples collected from manufacturing areas. salary: $45 - $58 per hour
shift: First
work hours: 8 AM - 5 PM
education: Bachelors Responsibilities Conduct biological, chemical, and physical analyses on samples including raw materials, initial, in-process and final products, and samples collected from environmental monitoring according to SOP and pre-approved protocols.
• Drive implementation of new methodologies, or new sample types into existing methods in a QC laboratory
• Support Investigation of nonconformances and troubleshoot unexpected results.
• Handle multiple tasks concurrently including testing and inventory management in a timely and appropriate manner.
• Perform review of test data, which includes overall documentation practices (CGDP). May perform release functions in LIMS or other computerized systems.
• Support generation and documentation of validation protocol deliverables.
• Draft and update, as required, QC SOPs.
• Perform test equipment, equipment maintenance and calibrations as required.
• May perform other duties as assigned. The essential functions of this role include:
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 View email address on 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.
shift: First
work hours: 8 AM - 5 PM
education: Bachelors Responsibilities Conduct biological, chemical, and physical analyses on samples including raw materials, initial, in-process and final products, and samples collected from environmental monitoring according to SOP and pre-approved protocols.
• Drive implementation of new methodologies, or new sample types into existing methods in a QC laboratory
• Support Investigation of nonconformances and troubleshoot unexpected results.
• Handle multiple tasks concurrently including testing and inventory management in a timely and appropriate manner.
• Perform review of test data, which includes overall documentation practices (CGDP). May perform release functions in LIMS or other computerized systems.
• Support generation and documentation of validation protocol deliverables.
• Draft and update, as required, QC SOPs.
• Perform test equipment, equipment maintenance and calibrations as required.
• May perform other duties as assigned. The essential functions of this role include:
- working in a smoke free environment
- wearing steel toe shoes
- manual lifting up to 50lbs
- standing for 5 hours at one time
- Quality Control
- Quality Assurance
- Laboratory/Sciences
- GMP manufacturing
- GDP
- Laboratory functions
- Product Inspection
- Production Control
- Pharmaceutical
- Years of experience: 2 years
- Experience level: Experienced
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 View email address on 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.
Vacancy posted 28 days ago
Similar jobs that could be interesting for youBased on the Quality Control Associate in Newbury Park, CA vacancy
$25 - $27 per hour
...Job Summary Under general supervision, this position performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good Manufacturing Practices (cGMP), safety guidelines, and regulatory requirements...SuggestedContract workWork at officeMonday to Friday- ...Check us out at We are looking for a motivated and hands‑on Quality Systems Specialist to join our team. How you will add value to... ...Supplier Qualification and oversight of quality Events and Change Control. The Quality Systems Specialist works closely with...SuggestedFull timeVisa sponsorshipWork visaMonday to Friday
- ...records in an audit‑ready state Assist with laboratory investigations including OOS results, deviations, invalid assays, and other quality system activities Support laboratory maintenance, calibration, housekeeping, and audit readiness activities Work cross‑functionally...Suggested
$45 per hour
...department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, drug...SuggestedHourly payPermanent employmentTemporary workWork experience placementLocal areaShift work$50 per hour
...advance your pharmaceutical career with a global industry leader? We are seeking a detail-oriented QC Analyst II to support critical quality control operations in a cutting-edge cGMP manufacturing facility. This is a fantastic on-site opportunity to drive analytical...SuggestedHourly payContract workTemporary workWork experience placementLocal area- ...are looking for a motivated and hands-on Quality Operations Specialist to join our team.... ...Review analytical data, test results, and associated documentation to support batch... ...CAPA development Manage and support change control activities, including impact assessments...Full timeVisa sponsorshipWork visaMonday to Friday
- SSi People is looking for an MCS Senior Associate Quality Assurance in Thousand Oaks, California. This role requires delivering real-time quality assurance support in a drug substance production facility. Responsibilities include providing compliance support and overseeing...Shift work
$75k - $112k
The Quality Assurance Specialist is responsible for planning, designing, executing, and documenting software testing activities across... ...based on contract needs Must comply with all ITAR/EAR export control regulations Background check required Avum, Inc. is an Equal...Contract workLocal areaRemote work- ...Job Description Job Description Job Summary: The Quality Specialist is responsible for creating, reviewing, and submitting First... ...with quality management systems (QMS) and documentation control ~ Familiarity with aerospace specifications and manufacturing...Work at office
$26 per hour
...Description Job Description At Cydcor, we’re committed to delivering exceptional experiences for our clients and customers. As a Sales Quality & Customer Support Specialist, you’ll play a vital role in improving customer outcomes, identifying quality trends, and helping our...Work at officeRemote work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Quality Control Associate. Be the first to apply!
Related searches
- quality equipment Newbury Park, CA
- quality manufacturing Newbury Park, CA
- quality tech Newbury Park, CA
- quality Newbury Park, CA
- quality inspection Newbury Park, CA
- quality control Newbury Park, CA
- qc Newbury Park, CA
- quality control nurse Newbury Park, CA
- quality control representative Newbury Park, CA
- qc engineer Newbury Park, CA

