Supervisor, QC Salary at Capsugel Sa BETA

12 Month Contract to Hire We're looking for a manufacturing operator with growth in mind. The company is expanding and is looking to promote manufacturing leads in the future. Responsibilities The incumbent is responsible for execution of all aspect of production operations which includes, but is not limited to, buffer preparation, drug formulation, filling, visual inspection, labeling, packaging, and sanitization. Gown for production operations to meet grades A, C & D cleanroom requirements. Interact with QC, QA, Tech services, Warehouse, Maintenance, IT, Supply Chain, and other departments as required. Visually inspect finished sterile product to identify any abnormalities or foreign particles or substances. Assist management in coordinating process activities to assure efficient, timely and smooth operations. Setup, operate, assess, and resolve minor equipment mechanical issues in the controlled classified areas. Monitor and maintain cleaning supplies and inventory to ensure availab

JOB TITLE: QC Sensory Technician DEPARTMENT: Quality Control REPORTS TO: QC Supervisor EFFECTIVE DATE: December 2024 SUMMARY: Conducts all necessary laboratory analysis prior to product release DUTIES AND RESPONSIBILITIES: Performs required sensory analysis. Assists with bench blending which includes project blends, possible inventory bulkings, and inventory reworks. Accurately weighs lab amounts for Production work orders. Performs office functions that include managing laboratory inventory levels and orders laboratory supplies. Manages the QC aspect of the incoming and outgoing samples. Oversees general laboratory housekeeping. Performs data entry of test results (when needed) Operates laboratory equipment (when needed) Performs other related duties as assigned by management. QUALIFICATIONS: Bachelor's Degree (BS) from four-year college or university, or one to two years of related experience and/or training, or equivalent combination of education and experience. Ability to read and

Job Description Job Description ABOUT SANISURE SaniSure is a multinational manufacturer of single-use bioprocessing solutions (SUT) used in the production of biological drugs, including monoclonal antibodies, cell therapies, gene therapies, and vaccines. With operations in the U.S. and in Europe, SaniSure operates a leading platform of vertically integrated critical fluid management technologies and integrated solutions. Its single-use products and system solutions are sold to global pharma and biotech companies and are used from R&D through full-scale commercial cGMP manufacturing of among the most innovative large molecule therapeutics and vaccines. This role is expected to be on-site. We continue to be on a robust growth trajectory, via both organic and inorganic growth, as the company capitalizes on increasing global demand and continues its transition from a component manufacturer to an integrated systems and solutions provider. Our primary offering includes high-value assembly so

Job Title: Associate IJob Description Perform testing to help develop methods for flow cytometry and analysis. Perform cell culture and cell counting to analyze for quality control. Help perform analysis for flow methods and complexity testing. Provide input to improve workflow and laboratory activity. Provide input and proficiency in relevant testing. Provide training and some oversight to new employees on the team. Perform the accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or efficacy of different cell populations. Perform maintenance, monitoring, and troubleshooting of pertinent equipment, including routine start-ups and shutdowns. Test, document, and report results for products or materials following company and/or client procedures under CGMP and/or GTP guidelines. Perform client proficiency testing under direct supervision as applicable. Organize the lab and put supplies away in a neat and organized manner

Job Type Full-time Description Position Summary Specialist III QA is a regular employee in a full-time exempt position at Kashiv Biosciences. The responsibility for document management lies with this role, including issuance and retrieval of logbooks, laboratory notebooks, issuance of protocol and report numbers, and management of documentation. The employee will support the activities of the QA department in review of QC data and reports, and other reports such as SOPs, CAPAs, Deviations, Change Controls and OOS as needed. Requirements Essential Duties & Responsibilities •Writes, revises, and reviews standard operating procedures (SOPs). •Conduct reviews of release testing, stability testing, raw material testing, method validations, equipment qualifications and calibrations, technical protocols and reports to ensure compliance with internal procedures and policies, good documentation practices (GDPs), current good manufacturing practices (cGMP), ICH, and other applicable regulations.

Job Description Job Description POSITION SUMMARY: Under the supervision of the QC Supervisor, this position will be responsible for scheduling Raw Materials, In-process and Finished Product samples for the testing according to the established QC guidelines and protocols. Candidate should be able to work in accordance with cGMP procedures and demonstrate a strong understanding of laboratory procedures and record keeping. ESSENTIAL FUNCTIONS: Responsible for submission of incoming samples for the testing in a timely manner for both in-house and contract labs, ensuring the accuracy of the testing requirements. Maintain proper logbook records to ensure all samples are received, logged, stored, scheduled and tracked per QC practices. Maintaining and storing electronic records of all sample submissions per the QC guidelines. Follow up for the testing status and setup a clear communication with QC Supervisor about any possible delays. Coordinate sample shipment to contract labs to ensure samp

**Regional Site Quality Manager - Renewables** Date: Oct 3, 2024 Location: US VA, US MD, US Company: Black & Veatch Family of Companies **Together, we own our company, our future, and our shared success.** As an employee-owned company, our people _are_ Black & Veatch. We put them at the center of everything we do and empower them to grow, explore new possibilities and use their diverse talents and perspectives to solve humanity's biggest challenges in an ever-evolving world. With over 100 years of innovation in sustainable infrastructure and our expertise in engineering, procurement, consulting and construction, together we are building a world of difference. **Company :** Black & Veatch Quality Control **Req Id :** 105346 **Opportunity Type :** Staff **Relocation eligible :** No **Full time/Part time :** Full-Time **Project Only Hire :** No **Visa Sponsorship Available:** No **Job Summary** By joining our BV Construction group, you will have the ability to develop and enhance your ski

PPG is a sister company of QISG under the parent Quanta Services, Inc. This posting is for a direct hire position of Phoenix Power Group and is solely for the purpose of Phoenix Power Group. Phoenix Power Group Inc. (PPG) is a leading Construction Services Company providing Engineering, Procurement and Construction (EPC) services specializing in the installation of utility and industrial process infrastructure including substations, power generation, industrial process facilities, and renewable fuel projects in North America. PPG is a subsidiary of Quanta Services Inc., the largest specialty contractor in North America, providing large single-source solutions and leading the industry in its ability to deliver a collective scope of services, expertise and manpower. PPG is an EPC contractor specializing in the installation of utility and industrial process infrastructure including substations, power generation, industrial process facilities, and renewable fuel projects. PPG utilizes a mo