(Biologics/cGMP) Quality Analyst

Job Title: Quality Analyst Location: Exton, PA Type: Contract Overview Join a pharmaceutical company operating globally in terms of R&D, manufacturing and marketing, with a strong focus on prescription medicines. Responsibilities The QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of...

Position Overview:The Quality Control Analyst will be responsible for ensuring compliance with cGMP standards in the quality control processes. This role requires a solid educational background and relevant experience in the biopharmaceutical industry.Qualifications: Bachelor’s degree in biological or chemical sciences or a related field. A minimum of 2-4...

Position Overview:The Quality Control Analyst at Lenmar Consulting Inc. plays a critical role in ensuring the integrity and quality of biopharmaceutical products. This position requires a solid educational background and relevant experience in a regulated environment.Key Responsibilities:Utilize a Bachelor’s degree in biological or chemical sciences or an...

Position Overview:The role of the Quality Control Analyst at Lenmar Consulting Inc. is essential in ensuring the integrity and compliance of our biopharmaceutical products.Qualifications: A Bachelor’s degree in biological or chemical sciences or a related field. A minimum of 2-4 years of relevant experience in a cGMP Quality Control, analytical...

Company DescriptionPharmaJob DescriptionBS in biological or chemical sciences or equivalent• Minimum of 2-4 yrs working experience in a cGMP Quality Control, analytical development, analytical transfer or validation department in a FDA-regulated industry.• Knowledge of principles, concepts, and practices in QC testing of protein biopharmaceuticals.•...

Job DescriptionJob Title: Quality Analyst IILocation: Exton, PADuration: 12 months contract with possible extensionDescriptionWill contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies. This individual has an important...

QC Analyst IIExton PA1-3 Year ContractThe QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies. The individual will help maintain the biochemistry laboratory systems, assist in training other...

Job DescriptionJob DescriptionDescription:The QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies. Biopharmaceutical manufacturing runs typically cost in excess of 1$ million each and reach many...

Job DescriptionJob DescriptionDescription:The QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies. Biopharmaceutical manufacturing runs typically cost in excess of 1$ million each and reach many...

Are You Ready to Elevate Your Career?Hired by Matrix is seeking a dedicated QC Analyst 2 to join a leading global pharmaceutical organization. We are committed to connecting talented individuals with companies that prioritize their contributions and foster positive work environments.Key Responsibilities:Ensure operational success by delivering precise,...

Job OverviewKey Responsibilities:Play a vital role in ensuring operational success by delivering precise, GxP-compliant evaluations of clinical biopharmaceutical products while engaging in assay qualification and validation initiatives.Recognize that biopharmaceutical manufacturing processes can exceed $1 million per run, particularly for larger phase 3...

Are You Ready to Elevate Your Career?At Hired by Matrix, we believe in more than just filling positions; we strive to connect talented individuals with organizations that appreciate their skills and contributions. With over three decades of experience in providing talent solutions, we partner with leading companies across various sectors, including...

CONTRACT MUST HAVES:BS in biological or chemical sciences or equivalent with 2+ years experience working in a cGMP Quality Control, analytical development, analytical transfer or validation department in a FDA-regulated industryHands-on experience with at least 2 of the following techniques: HPLC, capillary electrophoresis, ELISA, or SDS-PAGE, used for...

Position: Quality Control AnalystCompany: Integrated Resources, Inc (IRI)Overview:We are seeking a qualified individual with a solid background in analytical laboratory practices, particularly within the pharmaceutical manufacturing sector. The ideal candidate will have experience in in-process, release, and stability testing utilizing methodologies such as...

Job SummaryJoulé is seeking an experienced Process Technician to join our team in the manufacture of preclinical, clinical, and commercial biologics drug substances. As a Process Technician, you will be responsible for operating upstream equipment, maintaining accurate records, and ensuring compliance with company and government regulations.Key...

Description:The QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies.Education: BS in biological or chemical sciences or equivalentExperience:Minimum of 2-4 yrs working experience in a cGMP Quality...

Position Overview:The Quality Control Analyst II plays a crucial role in ensuring operational excellence by delivering precise, GxP-compliant evaluations of clinical biopharmaceutical products. This position also involves active participation in assay qualification and validation studies.Educational Requirements: A Bachelor’s degree in biological or...

Position Overview:The Quality Control Analyst 2 plays a vital role in ensuring the operational success by delivering precise, GxP-compliant evaluations of clinical biopharmaceutical products. This position also involves participation in assay qualification and validation initiatives.Given that biopharmaceutical manufacturing processes often exceed $1 million...

12-Month Contract $28.66/Hour Job Description:The QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies. Biopharmaceutical manufacturing runs typically cost in excess of 1$ million each and reach many...

12-Month Contract $28.66/Hour Job Description:The QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies. Biopharmaceutical manufacturing runs typically cost in excess of 1$ million each and reach many...