Yoh, A Day & Zimmermann Company
QC II/ Sr. QC Associate
Yoh, A Day & Zimmermann Company, San Diego, California, United States, 92189
Yoh Life Sciences is hiring for a
QC Associate II
contractor for 8 weeks in
San Diego
with our biopharmaceutical customer. The Quality Control Associate will be responsible for performing multiple tasks within the Quality Control (QC) group in support of GMP large‑molecule manufacturing activities. Focus areas include execution of analytical method qualification / validation protocols, routine analytical testing and documentation / data review of QC generated results.
Duration:
8 week temp Pay Rate:
$40 - 45/hr DOE Location:
San Diego Shift:
Monday - Friday 9am - 5pm
Responsibilities
Collaborates with AMO on method establishment and leads transfer into QC (e.g. method verification, qualification, transfers and validations). Executes qualification / validation protocols and writes technically sound qualification / validation reports.
Performs routine analysis and testing of in‑process, release and stability samples using a broad range of assays such as pH, osmolality, and appearance, as well as ELISA, HPLC methods (e.g. titer, SE‑HPLC, RP‑HPLC), CE‑SOS, SOS‑PAGE, and clEF, as needed.
Maintains a cGMP quality level of work for the QC operations to include training, documentation and procedural work.
Writes and reviews data, technical reports, deviations, OOS investigations and test results and provides conclusions and proposals for future directions.
Initiates quality records as needed and performs technical writing of investigations for deviations and out of specification reports.
Supports audit preparations and client requests as needed.
Ensures the maintenance of laboratory and instrumentation.
Maintains regular and reliable attendance on a full‑time basis.
Performs other related duties as assigned.
Exhibits professional behavior with internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Qualifications / Skills Required
Bachelor’s degree in chemistry or related field
Minimum of 5 years’ experience in GMP pharma/biotech facility
Experience with the use of analytical techniques / instruments, such as ELISA, High Performance Liquid Chromatography (HPLC), CE‑SOS and clEF (Maurice platform), etc.
Excellent written and oral communication skills
Basic computer knowledge, including Microsoft Word, Excel and PowerPoint
Ability to effectively organize, multitask, and work in a fast‑paced, deadline driven work environment
Demonstrated understanding of USP, EP and ICH guidelines
Ability to communicate in a proactive and solution‑focused manner, including keeping management aware of potential issues
Detail oriented with the ability to troubleshoot and resolve problems
Ability to work independently and manage one's time
Estimated Min Rate : $31.50 Estimated Max Rate : $45.00
What’s In It for You?
Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
Health Savings Account (HSA) (for employees working 20+ hours per week)
Life & Disability Insurance (for employees working 20+ hours per week)
MetLife Voluntary Benefits
Employee Assistance Program (EAP)
401K Retirement Savings Plan
Direct Deposit & weekly ePayroll
Referral Bonus Programs
Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit
https://www.yoh.com/applicants-with-disabilities
to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, 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. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:
https://www.yoh.com/privacy-notice .
#J-18808-Ljbffr
QC Associate II
contractor for 8 weeks in
San Diego
with our biopharmaceutical customer. The Quality Control Associate will be responsible for performing multiple tasks within the Quality Control (QC) group in support of GMP large‑molecule manufacturing activities. Focus areas include execution of analytical method qualification / validation protocols, routine analytical testing and documentation / data review of QC generated results.
Duration:
8 week temp Pay Rate:
$40 - 45/hr DOE Location:
San Diego Shift:
Monday - Friday 9am - 5pm
Responsibilities
Collaborates with AMO on method establishment and leads transfer into QC (e.g. method verification, qualification, transfers and validations). Executes qualification / validation protocols and writes technically sound qualification / validation reports.
Performs routine analysis and testing of in‑process, release and stability samples using a broad range of assays such as pH, osmolality, and appearance, as well as ELISA, HPLC methods (e.g. titer, SE‑HPLC, RP‑HPLC), CE‑SOS, SOS‑PAGE, and clEF, as needed.
Maintains a cGMP quality level of work for the QC operations to include training, documentation and procedural work.
Writes and reviews data, technical reports, deviations, OOS investigations and test results and provides conclusions and proposals for future directions.
Initiates quality records as needed and performs technical writing of investigations for deviations and out of specification reports.
Supports audit preparations and client requests as needed.
Ensures the maintenance of laboratory and instrumentation.
Maintains regular and reliable attendance on a full‑time basis.
Performs other related duties as assigned.
Exhibits professional behavior with internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Qualifications / Skills Required
Bachelor’s degree in chemistry or related field
Minimum of 5 years’ experience in GMP pharma/biotech facility
Experience with the use of analytical techniques / instruments, such as ELISA, High Performance Liquid Chromatography (HPLC), CE‑SOS and clEF (Maurice platform), etc.
Excellent written and oral communication skills
Basic computer knowledge, including Microsoft Word, Excel and PowerPoint
Ability to effectively organize, multitask, and work in a fast‑paced, deadline driven work environment
Demonstrated understanding of USP, EP and ICH guidelines
Ability to communicate in a proactive and solution‑focused manner, including keeping management aware of potential issues
Detail oriented with the ability to troubleshoot and resolve problems
Ability to work independently and manage one's time
Estimated Min Rate : $31.50 Estimated Max Rate : $45.00
What’s In It for You?
Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
Health Savings Account (HSA) (for employees working 20+ hours per week)
Life & Disability Insurance (for employees working 20+ hours per week)
MetLife Voluntary Benefits
Employee Assistance Program (EAP)
401K Retirement Savings Plan
Direct Deposit & weekly ePayroll
Referral Bonus Programs
Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit
https://www.yoh.com/applicants-with-disabilities
to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, 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. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:
https://www.yoh.com/privacy-notice .
#J-18808-Ljbffr