- Pfizer (Groton, CT)
- …faster by imagining what's possible and taking action. **What You Will Achieve** As a Sr . Associate Drug Product Manufacturing (DPM) Lead within Drug Product ... the scale-up of solid oral dosage forms from lab to GMP manufacturing scale (immediate release tablets, modified release tablets, microspheres, capsules, etc.)… more
- Amgen (Thousand Oaks, CA)
- …your best work alongside other innovative, driven professionals in this meaningful role. ** Sr Associate Manufacturing ** **Live** **What you will do** Let's ... drug substance manufacturing processes and procedures. Draft and revise GMP manufacturing documents (SOPs, Forms). Draft and develop user requirements… more
- Astrix Technology (Thousand Oaks, CA)
- Sr . Manufacturing Associate Manufacturing Thousand Oaks, CA, US Pay Rate Low: 30 | Pay Rate High: 38 + Added - 10/05/2024 Apply for Job Our client, a ... a fantastic opportunity to join the team as a Sr . Manufacturing Associate We are...control ownership, ensuring records are comprehensive and compliant per GMP regulatory procedures. This must occur with a Right… more
- Mayo Clinic (Jacksonville, FL)
- …equity and inclusion, and provides the resources you need to succeed. **Responsibilities** The Sr . Quality Analyst, FDA Regulated Manufacturing will be part of a ... GMP principles (eg, quality process analyst, quality improvement associate , etc.) is strongly encouraged. **Exemption Status** Exempt **Compensation Detail** $… more
- Amgen (New Albany, OH)
- …do your best work alongside other innovative, driven professionals in this meaningful role. Sr Associate Digital Manufacturing **Live** **What you will do** ... support the development of master batch records, technical reports, and other Good Manufacturing Practices ( GMP ) documents that supports smart manufacturing … more
- Lilly (Indianapolis, IN)
- …better for people around the world. **Organization:** Drug Product External Manufacturing Quality Assurance assures patients worldwide of safe and efficacious drug ... selection, pre-validation/validation, ongoing operations, and termination. Drug Product External Manufacturing Quality Assurance is committed to creating partnerships that… more
- Quality Consulting Group (Thousand Oaks, CA)
- …CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic ... you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: + New Product Introductions… more
- Astrix Technology (Milpitas, CA)
- Sr Manufacturing Associates Manufacturing ...a variety of Vascular Therapies. They are seeking a Senior Manufacturing Associate to play ... and quality records. + Adhere to and comply with Good Manufacturing Practices ( GMP ) and Good Documentation Practices (GDP). **Requirements:** + High School… more
- Terumo Medical Corporation (Elkton, MD)
- Sr . Manufacturing Operator, B Shift (6pm-6:30am), TR Band 2 Date: May 17, 2024 Req ID: 3128 Location: Elkton, MD, US Company: Terumo Medical Corporation ... for order and up-coming changeovers from Supervisor. Requires minimal supervision. Sr . Manufacturing Operator has responsibility for providing daily work… more
- Lilly (Lebanon, IN)
- …help to build the processes and facility to enable a successful startup into GMP manufacturing operations._ **Main Purpose and Objectives of Position:** The ... Sr ./ Sr . Principal HSE Associate /Engineer is...as the site grows through startup to full scale GMP manufacturing . Post start-up, this role will… more
- Aston Carter (Thousand Oaks, CA)
- …within the Site Supply Chain organizations and the RMD organization within External Supply Manufacturing . The Sr . Associate Supply Chain is responsible for ... Smart sheets or at the very least Excel and remain self sufficient. Amgen is seeking a Sr . Associate Supply Chain to be a part of our Global Raw Materials and… more
- Randstad US (South San Francisco, CA)
- sr . research associate , analytical development. + south san francisco , california + posted 5 days ago **job details** summary + $30 - $39.34 per hour + contract ... $30.00 - 39.34 per hour work hours: 9 to 5 education: Bachelors responsibilities: The Sr . Research Associate will be responsible for developing assays for the … more
- US Tech Solutions (New Albany, OH)
- …and SOP's * MS Office familiarity . **Preferred Qualifications** * Polished GMP professional with Warehousing, Manufacturing or Quality experience * Experience ... of GMPs, SOP adherence. 2. Biotech/Pharma experience 3. Material handling experience in a GMP environment 100% Onsite - New Albany, OH (Relocation is fine) 3 head… more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill an Associate Director of Quality Auditing position. This position will be responsible for providing professional expertise, ... oversight and planning for the Regeneron Quality Auditing function, with primary emphasis on GMP , IT and Quality audits that may impact GMP operations and/or… more
- Pfizer (Groton, CT)
- …manage resource requirements (FTE, capital assets, and capabilities) for drug product manufacturing . + Author, review or approve GMP documentation, including ... individual for the role of Operations Lead, Drug Product Manufacturing in our Groton CT facilities (SDM / PCMM).The...while meeting operational quality standards in alignment with current GMP guidelines. The candidate will work closely with other… more
- US Tech Solutions (Thousand Oaks, CA)
- …to deviations, safety events. Biotech, pharma, background. The Senior Associate Facilities Maintenance will provide support to Manufacturing Clinical Supply ... experience with facilities management or maintenance of a regulated Manufacturing Area ( GMP Manufacturing ) 2. Demonstrated experience with document revision… more
- Lilly (Durham, NC)
- …operations at Research Triangle Park Parenteral Manufacturing facility. The Sr Manager assists the Associate Director-QA Parenteral in managing daily ... facility and Quality System from the ground up. The Sr Manager for QA Visual Inspections Operations is responsible...occur within the parenteral areas. + Reviews and approves GMP documentation in support of daily operations such as:… more
- Lilly (Branchburg, NJ)
- …First & Quality Always; following our common purpose under TEAM Lilly and our Manufacturing Standards under the strict code of conduct guided by our Red Book ... works within the Lilly Branchburg Process Team environment per Manufacturing Standards for Operational Excellence (MSOE), resolves key technical/quality problems… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …SAP/Bioman, CIP, Compliance, and Scheduling. + **_Departments_** are defined as: Manufacturing departments. ** Sr . Technical Production Specialist** + BS/BA ... and services in more than 110 countries and regions. The Technical/ Sr . Technical Production Specialist is responsible for designing, developing, implementing,… more
- Boehringer Ingelheim (St. Joseph, MO)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Associate Director, Site MSAT strategically and technically leads all ... aspects of the site's MSAT ( Manufacturing Science and Technology) processes within the site to...minimum of eight (8) of MSAT/scientific experience within a GMP biological vaccine and/or pharmaceutical production environment. + Experience… more