Senior Manager, Quality Salary at Janatics Usa Inc BETA

SUMMARY/JOB PURPOSE: Responsible for assisting in the development, implementation and maintenance of QA systems and activities supporting GCP and PV operations. Provides assistance with planning and conducting audits of vendors and associated documentation activities. Essential Duties And Responsibilities: * Responsible for assisting in the development of internal processes and systems related to GCP and PV QA activities; * Provides direct support to clinical study teams and participates in QA planning and implementation to support study operations; * Participates in the development and approval for the CQA audit schedule including the contracting of PV and GCP audits to contractors and conducting complex audits; * Responsible for developing, tracking and managing periodic management reports including key Clinical and PV Compliance and QA metrics; * Participates in and support various development teams; * Manages and/or participates in complex audits and regulatory inspections; * Indep

Job Description Job Description Job Summary: Directly supervise hourly personnel during the production shift and satisfy all production, quality and safety requirements in the most economical manner possible. Responsibilities Plan, organize and control shift operations in accordance with Company policies and procedures. Maintain total awareness of Company policies, procedures and regulations, and ensure compliance by all assigned employees. Focus efforts toward the completion of production in accordance to the daily production schedule. Conduct operations to maximize production yield while minimizing loss of raw materials, supplies and components. Check equipment speeds at the start and throughout regular tours during the shift. Ensure the timely and accurate recording and submission of all necessary forms, reports and documents required for management reports. Provide continuous on-the-job development, training and motivation of personnel to acquire maximum quality, productivity, coop

**_General Description:_** Manages the operational performance of the Manufacturing QA function, ensuring the successful day to day management of: QA manufacturing shop floor activities, Batch Release Key processes and QA objectives, whilst adhering to regulatory compliance and achieving commercial success. Assists shop floor Mfg. associates with deviation management and batch documentation of events. The position also supports other QA duties or QA projects assigned according to business needs. To ensure the efficient and effective day to day running of the manufacturing QA Team. **_Essential Functions of the job_** **_:_** + Developing and implementing the Quality Assurance Batch Release strategy, to ensure it meets the business requirements and customer deliverables, as well as ensuring the departmental performance against goals. + Acts as the site Release Responsible Person, interacts with EU QPs as needed for European batch release. + Support QA shop floor activities with resource

Production Supervisor, 3rd shift Exton, PA (USA) (Onsite) Sunday-Thursday 10PM - 6:30AM As a Production Supervisor, you will assure that DSM products are of consistent and high quality by supervisor assigned areas in compliance with SHE and quality system requirements to achieve customer quality and service expectation. As the primary point of contact and guidance for operators who produce DSM medical devices, this position represents a critical link in ensuring company expectations are appropriately communicated, understood, and carried out by the team. The ideal candidate will have manufacturing experience within a medical device or pharmaceutical environment. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Responsi

Delivering mission-critical, electronic solutions that protect lives. Use your creativity and critical thinking to take our products from concept to customer. At CAES, we engineer solutions for the world's most critical missions. We serve customers in the defense and aerospace markets. Seeking a career that offers challenging, diverse projects and opportunities? Looking for a position with a company that offers long-term professional advancement? Searching for a place that values a diverse, team-based environment? One that values YOU. Consider CAES. The most important thing we build is TRUST Overview As a seasoned Senior Manager Manufacturing Engineering at CAES, you play a pivotal role in advancing our manufacturing processes and ensuring the highest standards of quality and efficiency. Your deep expertise in engineering and leadership is instrumental in driving innovation, optimizating production workflows, and achieving exceptional operational performance. You are not just a leader,

Company Description M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we've seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems. Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements. Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA. Due to our continued growth, we are hiring for a S

SUMMARY The Senior Specialist, QA Analytical ensures cGMP compliance and adherence to SOPs and WRKIs through the review and approval of compliance documentation. It also ensures company compliance in its programs to prevent or eliminate deviations in procedures. Additional responsibilities include review and approval of investigations, CAPAs, analytical lab documents, regulatory support and quality process improvement. ESSENTIAL DUTIES AND RESPONSIBILITIES Provide leadership, support and oversight of analytical lab documents, investigations, CAPAs, manufacturing, packaging, labels, release of material. Responsible for review and approval of analytical CoAs, reports, stability protocols, calibration notebooks and method transfers/development testing protocols. Responsible for the review, approval and logistics of pre-executed and post executed batch records through QA department. Review and approve documents, such as change control, change orders, component specification sheets to ensur

About Vibrantz Technologies Vibrantz Technologies ("Vibrantz" or "Company") is a leading global provider of specialty chemicals and materials solutions whose purpose is to bring color, performance and vibrancy to life. Every day, our employees, the products we make, and our valued customer partnerships are inspired by this purpose. Serving customers globally, our innovations are trusted in a variety of advanced materials, color solutions and performance coatings applications to enhance the hue, functionality, safety and environmental footprint of everyday consumer products. Our key competencies in particle engineering, glass and ceramic science and color technology enable benefits like more durable vehicles and batteries, easier-to-clean appliances, energy efficient roof tiles and bricks, stronger and more decorative glass, and eco-friendly paints. Headquartered in Houston, Texas, Vibrantz has over 60 manufacturing facilities and sales offices on six continents and employs roughly 4,00