Rose International
Date Posted:
12/11/2025 Hiring Organization:
Rose International Position Number:
494551 Industry:
Biotech/Healthcare Job Title:
Quality Control Specialist Job Location:
Berkeley, CA, USA, 94710 Work Model:
Onsite Shift:
M-F start 8:00am Employment Type:
Temporary Full-Time:
Yes Estimated Duration:
6 months Hourly Rate:
$32.00–$37.00
Must Have Skills/Attributes:
Chemistry, GDP, GMP, LIMS, Pharmaceutical
Experience Desired:
Pharmaceutical industry experience (3 yrs); Thorough knowledge of chromatography techniques (3 yrs); Comprehensive knowledge of GDP and GMP practices (3 yrs)
Summary Supports implementation of new methods in Quality Control Chemistry department.
Education / Experience Requirements
Minimum 6 years of experience in pharmaceutical or related industry with a Bachelor's degree, OR
Minimum 2 years of experience with a Master's degree, OR
PhD with relevant pharmaceutical industry exposure
Demonstrated hands‑on experience with analytical instrumentation in a regulated environment
Required Skills
Thorough knowledge of chromatography techniques including SEC, ION, NORMAL, REVERSE, and ION‑PAIR chromatography
Proficiency in electrophoresis methods including PAGE and agarose gel electrophoresis
Expertise in simple chemistry methods such as spectrophotometry
Strong understanding of biologics and pharmaceutical manufacturing processes
Hands‑on experience with LIMS, SAP, and EMPOWER chromatographic software
Comprehensive knowledge of GDP and GMP practices
Excellent documentation and technical writing abilities
Strong analytical and troubleshooting capabilities
Ability to manage multiple priorities and work independently
Effective communication and interpersonal skills for cross‑functional collaboration
Responsibilities
Support the implementation and integration of new analytical methods within the Quality Control Chemistry department
Maintain comprehensive logs, notebooks, and electronic documentation systems in accordance with regulatory requirements
Conduct method feasibility studies and method development activities to support analytical testing needs
Execute laboratory assays for method validation protocols utilizing various chemistry instrumentation
Operate and maintain analytical equipment including HPLC, UPLC, KF Titrator, Autotitrator, Melting Point meter, Chloride meter, and Polarimeter
Troubleshoot assays and analytical instrumentation to ensure optimal method performance and data quality
Prepare samples using wet chemistry techniques and various analytical methodologies
Generate comprehensive method development reports and method validation reports
Follow established SOPs, pharmacopoeial guidelines, regulatory requirements, and safety protocols
Manage multiple concurrent tasks while working effectively with technical leads across different projects
Interface and collaborate with manufacturing, research, and other cross‑functional teams
Utilize LIMS, SAP, and chromatographic software systems for data management and analysis
Only those lawfully authorized to work in the designated country associated with the position will be considered.
Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.
Benefits For information and details on employment benefits offered with this position, please visit the relevant HR portal. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website.
Equal Opportunity Employer Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E‑Verify). (Posting required by OCGA 13/10‑91.).
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12/11/2025 Hiring Organization:
Rose International Position Number:
494551 Industry:
Biotech/Healthcare Job Title:
Quality Control Specialist Job Location:
Berkeley, CA, USA, 94710 Work Model:
Onsite Shift:
M-F start 8:00am Employment Type:
Temporary Full-Time:
Yes Estimated Duration:
6 months Hourly Rate:
$32.00–$37.00
Must Have Skills/Attributes:
Chemistry, GDP, GMP, LIMS, Pharmaceutical
Experience Desired:
Pharmaceutical industry experience (3 yrs); Thorough knowledge of chromatography techniques (3 yrs); Comprehensive knowledge of GDP and GMP practices (3 yrs)
Summary Supports implementation of new methods in Quality Control Chemistry department.
Education / Experience Requirements
Minimum 6 years of experience in pharmaceutical or related industry with a Bachelor's degree, OR
Minimum 2 years of experience with a Master's degree, OR
PhD with relevant pharmaceutical industry exposure
Demonstrated hands‑on experience with analytical instrumentation in a regulated environment
Required Skills
Thorough knowledge of chromatography techniques including SEC, ION, NORMAL, REVERSE, and ION‑PAIR chromatography
Proficiency in electrophoresis methods including PAGE and agarose gel electrophoresis
Expertise in simple chemistry methods such as spectrophotometry
Strong understanding of biologics and pharmaceutical manufacturing processes
Hands‑on experience with LIMS, SAP, and EMPOWER chromatographic software
Comprehensive knowledge of GDP and GMP practices
Excellent documentation and technical writing abilities
Strong analytical and troubleshooting capabilities
Ability to manage multiple priorities and work independently
Effective communication and interpersonal skills for cross‑functional collaboration
Responsibilities
Support the implementation and integration of new analytical methods within the Quality Control Chemistry department
Maintain comprehensive logs, notebooks, and electronic documentation systems in accordance with regulatory requirements
Conduct method feasibility studies and method development activities to support analytical testing needs
Execute laboratory assays for method validation protocols utilizing various chemistry instrumentation
Operate and maintain analytical equipment including HPLC, UPLC, KF Titrator, Autotitrator, Melting Point meter, Chloride meter, and Polarimeter
Troubleshoot assays and analytical instrumentation to ensure optimal method performance and data quality
Prepare samples using wet chemistry techniques and various analytical methodologies
Generate comprehensive method development reports and method validation reports
Follow established SOPs, pharmacopoeial guidelines, regulatory requirements, and safety protocols
Manage multiple concurrent tasks while working effectively with technical leads across different projects
Interface and collaborate with manufacturing, research, and other cross‑functional teams
Utilize LIMS, SAP, and chromatographic software systems for data management and analysis
Only those lawfully authorized to work in the designated country associated with the position will be considered.
Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.
Benefits For information and details on employment benefits offered with this position, please visit the relevant HR portal. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website.
Equal Opportunity Employer Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E‑Verify). (Posting required by OCGA 13/10‑91.).
#J-18808-Ljbffr