SRG is currently looking for Sr Manufacturing Engineer for one of our priority clients! Reach out to me if you if you or anyone you know has interest! Beverly, MA(Direct position) Sr. Manufacturing Engineer JOB DESCRIPTION Responsible for creating, documenting, developing and implementing procedures used to assemble, process, test and /or manufacture products. Will design, implement, monitor and maintain manufacturing processes. Consult with design engineers in order to achieve the most efficient and cost effective way of producing the highest quality product possible. Qualifications BS in mechanical or manufacturing engineering. Engineering drawings/specifications and manufacturing process planning/evaluation. Prior experience in machine shop practices including milling, turning and grinding is preferred. Background in continuous improvement, project management, cross-functional work, facility and workstation design, resource scheduling and asset...

Quality Engineer - Medical Device Quality Engineering supports compliance with Regulatory and Procedural requirements identify trends requiring remediation and to recommend Preventive Actions to address them. Essential Functions and Responsibilities: Working directly with cosmetic/OTC CMOs to identify gaps in processes or procedures against GMP and Quality Agreements. Reports to QA manager based in Irvine, CA. Serve as Quality Person in Plant at local CMO (located in California) and may travel to additional CMOs within the continental US. Creation and implementation of Quality Improvement Plans to remediate deficiencies at CMOs. Trend Analysis of deviation and complaint investigations, and associated corrective actions. The development and execution of continuous improvement projects; and maintenance of defined QA metrics. Review of GMP documentation, including batch records, cleaning validation, SOPs, audit reports (internal/regulatory) and annual product reports....

Project Engineer - Power Distribution SRG Life Sciences is in need of Project engineer with Power Distribution experience for our priority client in Gaithersburg, MD. Individual must have Pharmaceutical/Biotech background. Reach out to me if you or someone you know has interest! Gaithersburg, MD 6-12 months Project Engineer with an Electrical Engineering background for a project Client is looking for a Project engineer with 5-10 years of bio/pharma experience. Client has several EE projects they are trying to complete before years end, will go into next year as well. Someone with a true EE...not automation/systems, more power distribution, wiring, motors, etc. #LI-BK1 SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

SRG is seeking a Senior Director, Supply Chain for a client in Bloomsbury, NJ. This position is with a growing pharmaceutical company , and qualified candidates will have 15+ years of related experience, preferably in the pharma industry. Position Overview: This position will work closely with the client’s executive team and functional leaders in developing strategies and processes, as well as oversee the implementation and management of the approved and agreed upon strategies and processes to ensure reliable, compliant, cost effective and on-time supply of products to meet business requirements. The position will have responsibility for the Supply Chain to ensure an uninterrupted supply of high-quality materials, the production planning of finished products aligned with the clients manufacturing strategy and network capacity and resource projections to ensure adequate lead-time to secure labor, equipment, materials and space based on growth, market conditions and regulatory...

We are searching for a Supply Chain Coordinator for a 12 month contract in Morrisville, NC The Supply Chain coordinator will develop and maintain integrated production planning and scheduling that encompasses materials to assure that they meet supply targets. This position will be responsible for ordering and buying materials as well as tracking production and material consumption in applicable system. MAJOR ACTIVITIES AND RESPONSIBILITIES: Develop dashboards by program, that track when program materials have been determined (PCL), ordered, received, tested and released Escalate roadblocks to any of these stages in the material process Work with each of the functions (mainly Supply Chain, QA and QC) to drive completion of deliverables for material readiness deadlines Work with the asset schedule planner to give input on ability to shift asset schedule based on material availability Develop, monitor and report key performance indicators around material and...

Biopharm Manufacturing JOB DESCRIPTION Role = Biopharm Manufacturing Associates Duration = One year from start date Work Shift = Candidates must be flexible to work various shift structures (days or overnight shifts), scheduled shifts will be assigned after training which three weeks M-F day shift. ASSIGNED SHIFT SCHEDULE: (Days or Nights) Week 1 = Sun, Mon, Thur & Fri Week 2 = Tue, Wed & Sat 100% onsite work (even during COVID with proper safety/health protocols) We believe in passionately working toward helping patients Do More, Feel Better, and Live Longer. We do this by supporting our energetic, dynamic teams. Under the direction of senior personnel, you will perform production operations including cell culture operations, preparation of media and buffer solutions, chromatographic separation, sterile filtration, and concentration operations. Work with various equipment including: bioreactors, tanks, chromatography columns, agitators,...

MES Recipe Developer The Emerson Syncade Recipe Developer will deliver electronic batch record configuration and validation in the Emerson Syncade Manufacturing Execution System (MES) and provide support for during batch record execution. Develop, validate, and deploy new and revised recipes in the Emerson Syncade MES system.Perform system configuration tasks and testing with supervision. Participate in validation activities including the development and execution of IQ/OQ/PQ protocols and testing. Perform dry runs and verification testing. Participate in cross-functional teams to assess and communicate planning, development, and testing solutions for recipe creation and modification. Perform support of floor operations on a rotational basis. Deliver updates to system lifecycle documents such as User Requirements Specifications, Configuration Specifications, Function Specification, Design Specifications.Work with local and network IT to develop and deliver...

SRG is a global staffing and consulting firm and we are looking for a Contract Quality Engineer IV, Risk Management-Medical Device in Dublin, CA! Envision working with energetic colleagues and inspirational leaders. We are always striving to find motivated individuals. Grow your career with the pharmaceutical and medical device industry leader! An ideal candidate for this role is someone who can thoroughly assess potential product risks and summarize them in a clear, concise manner; a natural ability to categorize information and see possibilities beyond the obvious would be helpful. Successful candidates will have the following types of experience: This role is part of the team that manages post-market medical device risk. As such, it is mandatory to have hands-on experience executing medical device risk management in alignment with ISO 14971 and QSR. Primary responsibilities of this position include aggregating and presenting periodic risk data, generating risk management...

Project Engineer SRG is in need of 2 Project Engineers for the Rockville area! Reach out to me if you or anyone you know has interest! Rockville, MD 6-12 + months Project Engineer Client is looking for a Project Engineer with 5-8 years of experience. General project engineering such as redlining drawings, data collection, support GES GA, order & procure equipment, draft PM task list, field verify/assess, receive internal permits. Pharma/Biotech (BSME or BSChE) #LI-BK1 SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.