Manager, Quality Salary at Bfgoodrich Inc BETA

Manage the KEMET Internal Quality Audit (IQA) system. Planning Execution/ Oversight Follow-up Reporting Oversight of the IQA team Help coordinate KEMET 3rd party quality certification audits, such as ISO 9001, IATF 16949, and AS 9100, by assisting ma Manager, Quality, Corporate, Technical Support, Technology

Job Summary The Quality Assurance Manager is accountable for organizing and maintaining quality control procedures and programs and to be responsive to sales and the market in order that demand for such programs is met. This position reports directly to the Operations Manager with dotted line reporting into the Corporate Director of Quality Management. Summary of Essential Job Functions/Responsibilities •Verify that inspection procedures by all warehouse personnel are accurate and in compliance with quality control procedures. •Establish quality control standards and procedures to be followed by the operations and sales departments and ensure that all necessary personnel are aware of these policies. •Inspect incoming and outgoing material to ensure that specifications are met, refusing any shipments that do not meet specifications. •Establish and maintain a program for providing actual chemical analysis for all carbon steel coils as the material arrives. •Inspect all returns and reject

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. JOB SUMMARY: QA Batch Record Specialist role supports fast-paced production environment to ensure controlled documents are managed as per standard processes and that product quality meets internal and regulatory requirements for release. Work schedule: Sunday, Friday, Saturday 6:00a - 6:30p High School diploma or GED required; higher learning certifications in an area relevant to role preferred. Minimum one (1) year of experience in a FDA-regulated manufacturing facility. Ability to read and interpret documents in English. Ability to perform calculations in all units of measure and understand rounding rules, significant figures, and tolerances to determine compliance with established criteria. Ability to use PC, calculator, and basic software (i.e., Microsoft Office); GMP software (e.g., Agile PLM, Oracle) experience p

**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

Must have experience with gas turbines LM6000 and LMXpress. Roles and Responsibilities Ensure that quality processes are fully implemented Perform site visit and spot quality control checks on the work in progress Assure the Site Quality documentation structure is set up and compliant to the contract (e.g. Site ITPs, Site ITPLs, Site Quality Plan) Lead all quality actions on site Represent the client Quality on site to the customer, authorities and any other external party Lead compliance actions on site and align required inspections and approvals Plan and lead site inspections Manage site documentation and assure on time delivery in good quality Lead Site Quality audits Set up an efficient quality team on site (Site Quality Engineer, Welding inspector) Provide quality assurance induction training to the site personnel With the assistance of third party or internal qualified Welding Supervisor, fully deploy welding processes and requirements Ensure that inspections / tests quality rec

JOB SUMMARY: To plan, organize and supervise the activities of auditing, in-process and finished product inspection in manufacturing and packaging to ensure regulatory compliance, safety and quality pharmaceutical products. The essential duties and responsibilities listed below are representative of those required on the job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties and responsibilities. ESSENTIAL DUTIES AND RESPONSIBILIITIES: Comprehend, maintain and promote cGMP and SOP compliance in FDA/DEA regulated pharmaceutical manufacturing environment, ensuring product integrity, safety and compliance standards. Manage and supervise the daily activities of the Plant Quality inspection team on all shifts to ensure oversight of operations process. Train, coach and mentor QA personnel, ensuing that training records are complete and accurate. Be proficient in all areas of manufacturing and packaging inspection process.

**The Opportunity** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. + Reporting compliance status data to operational quality management + Collaborate with center management in the development and implementation of continuous improvement plans + Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns + Responsible for coordinating and managing training activities, policies and processes at the center level. You will report to the Assi

QA Inspector job is to maintain the level of quality of the product which is being produced, bottled, and packed prior to shipment to PL Development's customers. Work schedule: Monday-Thursday 6a - 4:30pm OR Sunday, Friday, Saturday 6a - 6:30p JOB QUALIFICATIONS: High School diploma or GED required; Associates degree preferred Previous experience with QA a plus Excellent oral and written communication skills in English; fluency in Spanish is a plus Basic knowledge and understanding of cGMP Ability to work in a fast paced environment Ability to multi task Basic math skills Ability to work with limited supervision POSITION RESPONSIBILITIES: Inspection of initial product produced as it is bottled and released off the production line, checking for correct content, volume fill level, bottle size, verification of label, correct batch number, expiration date, verification packaging conforms to customer purchase order specs Report any errors or discrepancies to the Line Leader, Supervisor, and