TekWissen ®
Analytical Chemist/Quality control chemist
TekWissen ®, Berkeley, California, United States, 94709
Analytical Chemist/Quality Control Chemist
1 day ago Be among the first 25 applicants
This range is provided by TekWissen ®. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $32.00/hr - $32.00/hr
Job Title:
Quality Control Specialist
Duration:
9 Months
Job Type:
Temporary Assignment
Work Type:
Onsite
Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. This client is a German multinational Pharmaceutical and biotechnology company and one of the largest pharmaceutical companies in the world, headquartered in Leverkusen, and areas of business include pharmaceuticals; consumer healthcare products, agricultural chemicals, seeds and biotechnology products.
Job Description
Supports implementation of new methods in Quality Control Chemistry department.
Maintains appropriate logs, notebooks and other records including electronic documents.
Performs method feasibility studies, method development, and performs laboratory assays for method validation protocol execution utilizing various chemistry instrumentations (HPLC, UPLC, KF Titrator, Autotitrator, Melting Point meter, Chloride meter, Polarimeter).
Thorough knowledge of chromatography (SEC, ION, NORMAL, REVERSE, ION- PAIR, etc), electrophoresis (PAGE and/or agarose), simple chemistry methods (e.g., spectrophotometry) and wet chemistry to prepare samples.
Knowledge of biologics and manufacturing processes.
Troubleshoots assays and analytical instrumentation needed for method performance including HPLC, UPLC, KF Titrator, Autotitrator, Melting Point meter, Chloride meter, Polarimeter.
Prior experience in a QC laboratory and hands on experience with LIMS, SAP and related chromatographic software (EMPOWER).
Generates method development reports and method validation reports.
Understands and follows SOPs, pharmacopoeias, regulations, and safety guidelines.
Able to follow GDP and GMP practices.
Capable of managing multiple tasks, working effectively with more than one technical lead, interfacing with other functions such as manufacturing and research personnel.
Minimum Education Bachelor's Degree in a science or technical field.
Minimum Experience Minimum 6 years of experience or a Master’s degree and 2 years of experience or a PhD and zero years of experience in pharmaceutical or related industry or an equivalent combination of education and experience.
3+ years experience in the relevant (business need) technical and logistical specialty.
Qualifications
Minimum Education: Bachelor's Degree in a science or technical field.
Minimum Experience: 6+ years in pharmaceutical industry or equivalent.
Knowledge of chromatography and electrophoresis techniques.
Experience with QC laboratory, LIMS, SAP and chromatography software.
Familiarity with GDP, GMP, SOPs and pharmacopoeias.
Strong analytical and problem‑solving skills.
Excellent communication and teamwork abilities.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
Seniority Level Associate
Employment Type Contract
Job Function Other
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This range is provided by TekWissen ®. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $32.00/hr - $32.00/hr
Job Title:
Quality Control Specialist
Duration:
9 Months
Job Type:
Temporary Assignment
Work Type:
Onsite
Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. This client is a German multinational Pharmaceutical and biotechnology company and one of the largest pharmaceutical companies in the world, headquartered in Leverkusen, and areas of business include pharmaceuticals; consumer healthcare products, agricultural chemicals, seeds and biotechnology products.
Job Description
Supports implementation of new methods in Quality Control Chemistry department.
Maintains appropriate logs, notebooks and other records including electronic documents.
Performs method feasibility studies, method development, and performs laboratory assays for method validation protocol execution utilizing various chemistry instrumentations (HPLC, UPLC, KF Titrator, Autotitrator, Melting Point meter, Chloride meter, Polarimeter).
Thorough knowledge of chromatography (SEC, ION, NORMAL, REVERSE, ION- PAIR, etc), electrophoresis (PAGE and/or agarose), simple chemistry methods (e.g., spectrophotometry) and wet chemistry to prepare samples.
Knowledge of biologics and manufacturing processes.
Troubleshoots assays and analytical instrumentation needed for method performance including HPLC, UPLC, KF Titrator, Autotitrator, Melting Point meter, Chloride meter, Polarimeter.
Prior experience in a QC laboratory and hands on experience with LIMS, SAP and related chromatographic software (EMPOWER).
Generates method development reports and method validation reports.
Understands and follows SOPs, pharmacopoeias, regulations, and safety guidelines.
Able to follow GDP and GMP practices.
Capable of managing multiple tasks, working effectively with more than one technical lead, interfacing with other functions such as manufacturing and research personnel.
Minimum Education Bachelor's Degree in a science or technical field.
Minimum Experience Minimum 6 years of experience or a Master’s degree and 2 years of experience or a PhD and zero years of experience in pharmaceutical or related industry or an equivalent combination of education and experience.
3+ years experience in the relevant (business need) technical and logistical specialty.
Qualifications
Minimum Education: Bachelor's Degree in a science or technical field.
Minimum Experience: 6+ years in pharmaceutical industry or equivalent.
Knowledge of chromatography and electrophoresis techniques.
Experience with QC laboratory, LIMS, SAP and chromatography software.
Familiarity with GDP, GMP, SOPs and pharmacopoeias.
Strong analytical and problem‑solving skills.
Excellent communication and teamwork abilities.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
Seniority Level Associate
Employment Type Contract
Job Function Other
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