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The role of Document/Change Control Specialist include, but are not limited to: Document Management • Oversee the full lifecycle of controlled documents, including creation, review, revision, approval, issuance, and retirement. • Ensure documents are formatted, maintained, and distributed in accordance with company standards and procedures. System Administration • Administer and maintain the company’s Document Management System (DMS), including user access, permissions, and periodic system updates. • Troubleshoot system issues and liaise with IT or vendors as needed. Compliance & Audits • Prepare and provide documentation during internal, customer, and regulatory audits. • Ensure all controlled documents comply with applicable regulatory standards (e.g., FDA, ISO, cGMP) and company requirements. Version Control • Monitor and enforce proper version control practices, ensuring that obsolete or superseded documents are promptly removed from circulation. Document Archiving • Maintain both electronic and physical archives according to established retention schedules. • Index and catalog records to allow for accurate and efficient retrieval. Change Control • Administer the Document Change Request (DCR) process to ensure that changes are reviewed, approved, implemented, and documented appropriately. Record-Keeping • Maintain accurate records of product data, certificates of compliance, inspection reports, and other documents required for quality assurance and regulatory compliance. Training Support • Train employees on document control procedures, proper documentation practices, and effective use of the Document Management System (DMS). • Provide ongoing support to ensure adherence to company documentation standards. Key Skills & Qualifications • Attention to Detail: Ability to ensure accuracy, consistency, and completeness in all documentation. • Software Proficiency: Skilled in document management systems (e.g., SharePoint, MasterControl) and Microsoft Office Suite (Word, Excel, PowerPoint). • Quality System Knowledge: Familiarity with quality management systems (QMS) and regulated manufacturing environments, including FDA, ISO, and cGMP requirements. • Manufacturing Awareness: Understanding of manufacturing workflows and quality control principles to align documentation with operational needs. • Communication Skills: Strong interpersonal and written communication skills for collaborating with cross-functional teams and training staff. • Organizational Skills: Ability to prioritize, manage deadlines, and maintain meticulous records in a fast-paced environment. Pay : $20.00 Hours: 7 a.m. to 3:30 p.m.

QC People are Needed to Learn our Production Quality Operations and Product Development at Our Manufacturing Plant. Hands On Positions that Requires Some QC Background and Experience in Manufacturing. Tremendous Career Opportunity for someone who enjoys Contributing to the Manufacturing Process and Attaining Team Goals. Great Benefits, a Healthy Work Environment, and Unequaled Job Security with a Company that has had Continued Growth and Success for over 50 Years. Please submit your resume and or Job History. You can also pick-up a Job Application at our Security Post at 15853 Olden St Sylmar, Ca 91342, 24 Hours a Day, 7 Days a Week. Reference Jobs 537-10

Assembler – Medical Device Manufacturing (Second Shift) Valencia, CA Are you detail-oriented and looking to grow in the medical device industry? We’re hiring Assemblers to join our dynamic team in Valencia, CA. As part of a leading medical device company, you'll contribute to the production of life-changing products that support patient health and safety. Key Responsibilities: Perform precise assembly of medical devices using hand tools, microscopes, and assembly equipment Follow detailed manufacturing instructions, blueprints, and SOPs Maintain high standards for quality, cleanliness, and safety in a controlled environment Document work accurately and follow GMP and ISO standards 🔧 Requirements: Minimum 1 year of hands-on assembly experience (medical device, electronics, or similar preferred) Excellent attention to detail and fine motor skills Ability to work effectively as part of a team in a fast-paced production environment Must be able to read and understand work instructions in English 2nd Shift | Monday – Friday, 3:00 PM – 11:30 PM $19.80 per hour Apply today Call or text 818-203-9268 and submit your resume for consideration

A&R Engineering has multiple openings for 2nd Shift Mechanical Assemblers for Aerospace and Defense components. - candidate must be capable of reading and understanding written and verbal instructions in English - candidate must be either as U.S. Citizen or permanent resident - candidate must have completed High School or GED as a minimum - Good manual dexterity is a must - Capable of lifting 15- 20 pounds - Training is available - Experience utilizing mechanical and pneumatic presses for riveting and staking is a plus - Experience utilizing automated identification equipment is a plus - Experience using basic measuring tools is a plus (i.e. - calipers, micrometers, vision systems) Principals only. Recruiters, please don't contact this job poster.

Assembly position using basic hand tools to assemble various components in quantity, with a possibility of on-the-job training across other areas of manufacturing. It's a growing company with a great culture, and very low employee turn over to prove it. Clean, modern facility is enjoyable to work in. Pay depends on experience, starting at $16/hr but can go up if you have added relevant experience. Paid vacation, 401k, health and dental, overtime, and bonuses are available. Must be US citizen and 18 years or older.

Starting Rate $18.22 - higher rate with more experience. This Assembler Position uses basic hand tools to assemble various components in manufacturing. We will provide on-the-job training to the right candidate. ControlAir is an established company with 35 years in the business. We have very low employee turnover, which is a testament to our exceptional culture and a clean, climate-controlled work environment. Candidates must be US citizens, 18 years and older. Candidates must be fluent in reading, writing, and speaking English.