Document Control Specialist Salary at Houdini Inc BETA

Jr Documentation Specialist - Batch records (Pharma, Biotech, Medical Device) Irvine, CA 92618 (Local candidates only. Onsite) $27-$32hr (Weekly pay + Benefits) 9 months contract (Excellent potential for permanent) Full- time: M-F 7am-3:30pm Our client is a global team of innovators, leaders, creators, builders, and problem solvers. They develop state-of-the-art instruments and reagents for life science research laboratories and healthcare facilities all over the world. Together they are helping people everywhere live longer, healthier lives. This position will be responsible for supporting the manufacturing of products by creating/processing/reviewing production batch records following established GDP/GMP processes and procedures. How You'll Make An Impact: Reviews documents for format, accuracy, and compliance with existing procedures, providing feedback on content as appropriate in collaboration with area experts. Coordinates with team members to efficiently process Change requests

Mortgage Document Control Specialist – Quality & Compliance Are you an experienced Mortgage Document Control Specialist looking to apply your expertise in mortgage and document custodian operations? We are seeking a detail-oriented Mortgage Document Control Specialist to ensure accuracy, compliance, and integrity in our processes. As a Mortgage Document Control Specialist, you will play a crucial role in maintaining industry standards by meticulously auditing and verifying mortgage documents. Key Responsibilities: Perform comprehensive audits on mortgage documents and custodial records. Verify documentation accuracy and compliance with industry regulations. Identify and correct discrepancies in loan files and records. Collaborate with team members to improve quality control processes. Generate detailed reports on audit findings and recommend process enhancements. Assist in training and mentoring new staff on quality control standards. Conduct training sessions to reinforce compliance a

Job Description Job Description Job Title: Document Control Specialist / QA Admin Shift: 2nd Shift (2:15 PM – 10:45 PM) Pay Rate: $23 - $25 per hour (depending on experience) Position Overview: We are seeking a detail-oriented and highly organized Document Control Specialist / QA Admin to join our quality assurance team on the 2nd shift. In this role, you will play a key part in ensuring accurate documentation, compliance with quality standards, and supporting the smooth operation of QA processes. This is an excellent opportunity to grow your career in a dynamic and collaborative environment while making a direct impact on operational excellence. Key Responsibilities: Manage, organize, and maintain controlled documents, ensuring accuracy, proper labeling, and version control. Ensure all documentation complies with industry regulations, company policies, and quality standards. Coordinate document reviews, approvals, and updates, working closely with cross-functional teams. Assist with Q

The Quality & Heath, Safety and Environmental (HSE) Manager will be responsible for developing, implementing and managing the company's quality system and ensuring compliance with selected industry standards and certifications decided by the company. This includes developing and driving process improvements internally and at suppliers, leading quality control initiatives and collaborating with cross-functional teams to achieve the highest levels of product integrity. The candidate will also implement and oversee the Heath, Safety and Environmental corporate programs. The ideal candidate will bring expertise in quality management, compliance and certification processes, as well as HSE procedures and best practices, particularly in a fast-paced startup environment. Responsibilities: Quality Management: • Establish and implement a comprehensive QMS, ensuring compliance with ISO standards (e.g., ISO 9001) for the operations in California. • Develop standard operating procedures (SOPs) and

GENTEX AT A GLANCE: At Gentex Corporation, we've created an environment where great ideas and great people can thrive. Leveraging a history that spans over 130 years, Gentex is a global leader in personal protection and situational awareness solutions for defense forces, emergency responders, and industrial personnel operating in high performance environments. Join our multinational team of exceptional and dedicated employees around the world and work on challenging and rewarding projects, grow your skills, and advance your career all while making a positive difference in the lives of our customers. Together, you and Gentex can build a career that's uniquely yours. ABOUT THE JOB! The Technical Document Specialist works closely with and assists the engineering team to create drawing and ECO's and manages the release, change and obsolescence of engineering controlled and related external documents. The individual creates and updates models and engineering drawings to support new product

At huMannity Medtec we truly understand the need for balance and, among other things and offer a 9/80 schedule with every other Friday off. That’s 26 long weekends a year! Position Summary: Seeking an additional Document Control Specialist to join our team as we are growing!. This role is responsible for administering and maintaining the company’s-controlled documents, records, and the document control system in accordance with company requirements. This position is a key role in ensuring product and quality system documentation meets defined quality standards requirements. This position also supports all documentation activities including review and release of change requests and provides guidance to users of the document control processes. Summary of Main Responsibilities: Reviews documents for completeness and identifies issues such as typos, grammatical errors, incomplete data, formatting discrepancies etc. and edits documents on behalf of the originator to correct the issues ident

Job Description Job Description Jr Documentation Specialist - Batch records (Pharma, Biotech, Medical Device) Irvine, CA 92618 (Local candidates only. Onsite) $27-$32hr (Weekly pay + Benefits) 9 months contract (Excellent potential for permanent) Full- time: M-F 7am-3:30pm Our client is a global team of innovators, leaders, creators, builders, and problem solvers. They develop state-of-the-art instruments and reagents for life science research laboratories and healthcare facilities all over the world. Together they are helping people everywhere live longer, healthier lives. This position will be responsible for supporting the manufacturing of products by creating/processing/reviewing production batch records following established GDP/GMP processes and procedures. How You'll Make An Impact: Reviews documents for format, accuracy, and compliance with existing procedures, providing feedback on content as appropriate in collaboration with area experts. Coordinates with team members to effi

Salary: $17.00 - $21.00 Hourly Location : Huntington Beach, CA Job Type: Temporary Job Number: 24/25 FWS Student Pool - GWC Division: Golden West College Opening Date: 07/12/2024 Closing Date: 6/30/2025 11:59 PM Pacific Definition About Golden West College Located in beautiful , Golden West College is a two-year college, serving over 10,500 students on a 122-acre campus. GWC offers over 60 Associate degrees, a strong university transfer program, more than 40 Career and Technical Education certificates, community education, and extensive student support services. Founded in 1966, Golden West College has been widely recognized for its pioneering leadership in designing learning-centered programs and services for its students. Additionally, GWC is an officially designated Hispanic-Serving Institution (HSI) and has an eligibility designation as an Asian American Native American Pacific Islander-Serving Institution (AANAPISI). At Golden West College we are committed to providing high qualit