GMP Documentation Expert

About the RoleWe are seeking a highly skilled and motivated MCS Manufacturing Associate to join our team. In this role, you will be responsible for performing various tasks related to manufacturing operations, including setting up and cleaning equipment, preparing buffers/media, and following GMP documents.

At ACL Digital, we offer a competitive salary of $120,000 annually to our Device Engineer. 100% Thousand Oaks-based role open to relocation candidates with standard shift hours from 8-5pm and potential for overtime. Ideal candidate has hands-on experience in engineering environments, particularly with tools like Instron systems and optical measurement...

Discover International is currently seeking two skilled professionals to fill the role of Document Control CoordinatorThe selected candidates will be responsible for ensuring the quality and compliance of electronic batch records, SOP revisions, work order approvals, and minor deviations. They will also evaluate compliance issues, provide recommendations,...

Job Overview:As a Sr Software Engineer at Aditi Consulting in Thousand Oaks, you will play a vital role in supporting our Drug Substance Supply organization. This manufacturing support role requires expertise in electronic batch record generation, validation, and communication between GMP operations teams and process development scientific groups.The ideal...

Company OverviewAditi Consulting is a leading consulting firm that provides expert services in digital transformation, manufacturing systems, and process development. Our team of experts has extensive experience in implementing electronic batch records, managing NPI/EBR metrics, and enhancing communication between GMP operations teams and scientific groups.

Job DescriptionRole Summary: We are seeking an experienced Sustaining Engineer Expert to join our team at Planet Pharma. This is a 12-month contract opportunity with the possibility of extension or conversion to a permanent position.Salary: $38/hour (W2)Responsibilities and Duties:Product Changes: Complete product and manufacturing process changes, ensuring...

Job OverviewWe are seeking a skilled Expert Systems Developer to join our team at Liberty Personnel Services, Inc.The estimated salary for this position is $120,000 - $180,000 per year, depending on experience.About the RoleThis is a key opportunity for an experienced systems engineer looking to leverage their skills in software development and systems...

Senior Analytical ScientistWe are seeking a highly experienced Senior Analytical Scientist to establish and lead the analytical development program suitable for Quality Control functions in the area of protein biotherapeutics for future GMP production.About UsThe O'Connor Group is an early-stage biopharma company creating breakthrough protein-based drugs to...

About the RoleThe Production Operations Associate will work closely with our manufacturing team to support the development, clinical, and commercial activities of our company. This role requires a strong understanding of GMP documents and procedures, as well as excellent communication and teamwork skills.

Job Summary: We are seeking a highly skilled Digital QMS Expert to join our team at Aditi Consulting. As a key member of our organization, you will be responsible for managing the collaboration on process improvement, transfer, and sustainment of QMS processes across company Operations and R&D. This involves ensuring the Digital QMS platform is up-to-date...

Job Description:We are seeking a skilled and detail-oriented Regulatory Compliance Expert to oversee and ensure adherence to regulatory standards within our organization. The ideal candidate will possess a strong background in quality management and compliance, with a focus on FDA regulations, CGMP, and various quality systems. This role is critical in...

Job Summary:Aditi Consulting is seeking a highly skilled Sr Software Engineer to join our team in Thousand Oaks. In this critical role, you will be responsible for generating electronic documentation, tracking NPI/EBR metrics, and facilitating communication between GMP operations teams and process development scientific groups.The ideal candidate will have...

Job OverviewImmediate opportunity for an MCS Quality Assurance (QA) Associate supporting one of the world's leading biotechnology companies located in Thousand Oaks, CA.A great company is seeking a highly motivated and detail-oriented individual to provide operational QA support of a clinical drug product packaging and labeling team as a MCS Quality...

**Job Summary** We are seeking an experienced Device Design and Development Professional to join our team at Aditi Consulting. This role offers the opportunity to work on commercialized drug delivery devices and participate in design, development, and lifecycle management activities. **Responsibilities** Design Control Expertise: Possess a deep...

About Amgen SAAt Amgen SA, our mission is to serve patients living with serious illnesses by developing innovative treatments that make a lasting impact on their lives. We have been at the forefront of biotechnology since 1980, pioneering new treatments for some of the world's toughest diseases.We have a collaborative and science-based culture that fosters...

About the Role:We are seeking a highly motivated Production Associate to join our team at Randstad Life Sciences. This role involves working in a dynamic production environment supporting development, clinical, and commercial activities. Under general supervision, the successful candidate will perform operations in the Manufacturing area according to...

Company Overview:EPM Scientific - Phaidon International is a leading global recruitment firm specializing in scientific and engineering placements.Job Summary:We are currently seeking a highly skilled Sr. Pharmaceutical Scientist - Manufacturing Process Leader to join our team. This role will be responsible for assisting the Manufacturing Sciences Department...

Key ResponsibilitiesA successful MCS Quality Assurance (QA) Associate will possess a strong understanding of GMP processes and documentation, excellent communication skills, both written and verbal, and experience with procedure reviews and initiation of deviation reports. Some of the key responsibilities include:• Review and approval of printed clinical...

VICTORY HEMATOLOGY AND ONCOLOGY INC is looking for a skilled Healthcare Claims Processor to join our team. As a Medical Biller, you will be responsible for processing insurance claims, maintaining accurate records, and ensuring timely payments. You will work closely with clients to answer questions related to billing, process all forms needed for insurance...

Job Summary">Midatlantic Employers' Association is seeking an experienced Software Development Engineer to join our team. This role requires a professional with expert-level skills in software architecture design, software analysis, and code development for embedded systems.">About the Role">We are looking for a talented individual who can take lead roles in...