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Job title-Manufacturing Operator (FBD, Granulation & Coating) Job location - Central Islip, NY Shift-1st & 2nd Note- Interview Drive scheduled for this job on 12/09/2025 Essential Duties and Responsibilities: • Dispensing raw materials and primary packing materials as per work order., • Ensure the proper planning and execution of batches., • Monitoring cleaning and sanitation of production area and machinery as per respective SOP during batch-to-batch and product-to-product changeover., • Daily monitoring and recording of production materials and production lines., • Conducting in-process checks and recording in batch manufacturing record., • Controlling machine operations with minimum rejections and maximum outputs while maintaining quality standards within the standard norms., • Operating equipment and performing necessary maintenance on machinery., • Safeguard equipment for smooth functioning with coordination of engineering for preventive maintenance and calibration., • Manufacturing and filling of products as per Batch Manufacturing Records and SOP., • Maintaining inventory of machine parts, tools, and accessories., • Working individually and in collaboration with others as part of a team., • Coordinating with other departments like packaging, engineering, QA, and QC for better planning and execution., • Sampling as per schedule and in coordination with QA and QC., • Check and ensure status labels at all stages of manufacturing and filling., • Identifying and assisting in any corrective actions., • Perform, check, and ensure calibration/verification of instruments, equipment, and weighing balances as per schedule., • Ensuring line clearance during batch-to-batch and product-to-product changeover., • Online documentation and timely entries related to manufacturing and filling operations and activities., • Wearing appropriate PPE as stated in the SOP before entering any processing areas., • Executing procedures to complete tasks safely and efficiently., • Performing duties through the proper safe use of equipment, according to Health & Safety procedures and Equipment Manuals., • Performing other related duties as assigned. Other Responsibilities: • Maintaining 100% cGMP and SOP Compliance during complete operation hours., • Complying with all company policies and procedures., • Reporting all issues that arise to the department head or reporting manager., • Performing daily maintenance on equipment and machinery., • Completing all documentation in a timely manner, ensuring their integrity, accuracy, and completeness., • Maintaining discipline in the department., • May be required to assist in the training of other employees in the department., • Flexible to work extended hours, to achieve manufacturing schedule when needed. Training and Safety: All employees must undergo various training activities at the start of their employment. New training and re-training will occur periodically. Operators may be required to cross-train in all areas of the manufacturing operations. Employees must strictly adhere to all safety, health, and environmental guidelines at all times and ensure that all safety precautions are being taken during the handling of machines. Qualification: • A high school diploma or equivalent is required., • An accredited college certificate or university degree is preferred., • A minimum one (1) year of manufacturing experience with Oral Solid Dosage is required., • Proficient in the English language (Speaking/Reading/Writing) to understand work instructions and document results., • Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment is highly preferred., • Basic understanding of mechanical machinery and the operating principles of control systems., • Ability to follow both verbal and written instructions., • Demonstrated ability to work in both independent and team environments., • Good knowledge of Health & Safety procedures, including, OSHA., • Strong mathematical and organizational skills. Physical Requirements: • This position requires the ability to do heavy lifting/bending frequently., • Exert an amount of force continuously and/or up to 5 pounds of force frequently and/or up to 25 pounds of force occasionally and/or up to 50 pounds of force rarely by utilizing a hand truck to lift, carry, push, pull or otherwise move objects., • The ability to wear appropriate PPE is required., • Individuals may be required to wear respiratory devices that include but are not limited to: Air Purifying Respirators (APR) which include half-face and full-face negative pressure respirators, hooded powered air-purifying respirators, or Supplied Air Respirators (SAR), which include hooded or full face supplied air respirators.

Job Description QA Intern – Fall 2025 Job Summary: We are seeking a detail-oriented and proactive Quality Assurance Intern to support our QA team, with a primary focus on reviewing, revising, and maintaining Standard Operating Procedures (SOPs). This role provides hands-on experience in the highly regulated Aerospace and Defense industry, while building core skills that are widely applicable across sectors such as automotive, healthcare, manufacturing, and software. The compensation for this role is $20-$22 hourly based on experience. Key Responsibilities: · Assist in the review, editing, and updating of SOPs to ensure clarity, consistency, and compliance with internal standards and regulatory requirements. · Collaborate with subject matter experts (SMEs) to verify accuracy of SOP content. · Help organize and maintain the SOP library in the document control system. · Participate in internal audits and help track document-related corrective and preventive actions (CAPAs). · Provide administrative support to the QA team, including preparing reports and summaries related to SOP status. · Attend QA team meetings and contribute to ongoing quality improvement initiatives. Preferred Qualifications: · Current enrollment in a Bachelor's or Master’s degree program in Quality Assurance, Life Sciences, Engineering, Business, or a related field. · Strong written and verbal communication skills. · Excellent attention to detail and organizational abilities. · Proficiency in Microsoft Office Suite (Word, Excel, etc.). · Ability to work independently and manage multiple tasks. What You Will Gain: · Practical experience working with a professional QA team · Exposure to compliance documentation and quality system processes · Opportunity to improve skills in technical writing and internal communication · A solid understanding of the role of SOPs in maintaining product and process quality

Job DescriptionDescription: For more than 75 years, Heatherwood has been committed to building upscale residential rental communities, commercial properties, and luxury urban spaces. Our commitment to quality constructions, striking designs, and providing exemplary service, makes us one of the most highly regarded leaders in the industry. Additionally, we offer a competitive benefits package including health & dental, and vision insurance, 401(k), and paid PTO. The Coordinator Manager supports the Development and Construction departments by managing day-to-day construction projects, ensuring efficient communication across departments, and collaborating with internal and external stakeholders, vendors, and others with whom we do business. This role leads and mentors a small team of Development / Construction Coordinators, providing guidance, oversight, and support. The Coordinator Manager plays a key role and is vital in delivering successful project outcomes. Responsibilities and Duties • Serve as the primary point of contact among Development/Construction staff, vendors, consultants and others with whom we do business., • Mentor and Supervise a small team of Construction/ Development Coordinators, providing day-to-day supervision, guidance, and support to ensure successful project execution and departmental efficiency., • Ensure compliance with budgets and schedule., • Maintain and update Standard Operating Procedures (SOP) as required., • Prepare and submit building permit applications., • Attend legal hearings related to violations and variances., • Provide weekly project status updates at Development/Construction meetings., • Draft and track requests for information (RFI)., • Maintain project documentation, including proformas, construction plans, status reports, and photo documentation, • Obtain Certificates of Occupancy upon project completion., • Collect and organize competitive bids from vendors and subcontractors., • Prepare, review, and process Contracts and Purchase Orders., • Draft and track change orders throughout the project lifecycle., • Support the Development / Construction departments with various administrative tasks., • Coordinate the pre-qualification and registration process for potential bidders, suppliers, and subcontractors., • Ensure Coordinators are appropriately trained and engaging trades and vendors early on so that all warranty information is in the que prior to project close out, ensuring a glitch free transition from construction to Operations, • Assist in the preparation of internal and external reports, including project budgets, cost reports, and other required documentation., • A minimum of seven (7) years of experience in pre-construction through project completion., • Expediting experience is a plus. Experience with municipal permitting processes and coordination with public agencies and utility companies for rebates procurement, • Experience with Yardi Voyager is a plus., • Ideal candidate has expertise in Procore, particularly for the purpose of soliciting bids, • Self-motivated, self-directed, and able to initiate tasks like informing executive team of draft SOP’s and gaining approvals without supervision., • Strong understanding of property budgets and budget compliance., • Strong interpersonal, business, and communication skills (both written and verbal)., • Excellent computer proficiency, including Microsoft Office Suite (Word, Excel, Outlook) Microsoft Project, DocuSign, • Ability to read and understand blueprints, • Familiar with AIA documents , lien waivers, insurance requirements, and compliance tracking., • Strong analytical and problem-solving skills, with a keen attention to detail., • Excellent organizational abilities and experience managing a high volume of work in a fast-paced environment., • Working knowledge of multi-family residential and mixed use projects is a plus., • Must have a valid driver’s license, • Ability to lift and carry up to 10 pounds occasionally, • Position is in -person and requires travel to job sites on occasion/as needed.

Job Description Job Summary: This position is a shared position. The primary duties are as a general labor employee in production. This position will fill in as a QA Technician when needed. Oversee the production process, ensuring safety and quality standards are met. Required Skills/Abilities: • Prior food service industry experience is a plus., • Must have good written, verbal, and math skills., • Responsible for daily QA function within a food processing plant., • Daily, perform a pre-operational sanitation checklist for buildings A, B, C, and D, • Perform an operational sanitation checklist for buildings A, B, C, and D for the duration of each production day., • Monitors production compliance to HACCP Plan, • Perform ATP test after deep cleaning procedures and after allergen productions. Determine conformance or nonconformance and take corrective action when necessary., • Check traceability records compared with actual lot numbers and correct any discrepancies., • Periodic audit of Recipes to see if followed., • Periodic line studies to pinpoint sources of increased micro count on product., • Collect and maintain reference samples for all products manufactured daily for freezer storage., • Collect records from the previous day's production., • Check the thawing process and document., • Check all temperatures around the facility and record on the Daily Temperature Log sheet and Pre-shipment HACCP record (2x Daily- am. / p.m.), • Take aseptic raw material and finished good samples for microbiological analysis., • At least every hour makes a production inspection for (if specifications are met):, • The thickness of the dough, • Raw product integrity, • Internal product temperature (when applicable)., • Organoleptic inspection., • Cooling tank operating, • Product condition after the freezer, • Packing machine operation, package seals, • Proper film bag, bag code date, • Box label and code date, • Metal detector, • Weight, • Employee dress, • Floor area, • Monitor all areas of production, • Water pick up when doing Precooked items., • Perform pH testing and Bostwick (Sauce plant), • When product is out of specification, put product on HOLD following SOP., • When Metal Detector rejects product, QA must inspect product following SOP, • Check sanitizer concentration once a week., • Check soap concentration once a week using a test kit., • Ability to understand documents such as safety rules, operating and maintenance instructions, and procedure manuals, • Ability to write routine reports and correspondence

Job Description Job Title: QA Inspector Location: Central Islip, NY (Additional openings in Hauppauge) Job Type: Permanent We’re looking for a detail-oriented QA Inspector to join our team and help ensure the highest standards of quality and compliance across our manufacturing operations. In this role, you’ll be responsible for performing inspections, verifying documentation, and supporting daily quality assurance activities in a fast-paced pharmaceutical environment. Key Responsibilities: • Perform pre-activity checks for room and equipment cleanliness., • Conduct daily walkthroughs of the warehouse to ensure compliance with internal standards., • Accurately document cleaning activities in logbooks and checklists., • Review QA release reports and physically release materials accordingly., • Verify incoming materials against documentation and labeling requirements., • Monitor and manage the reject cage., • Perform daily balance verifications., • Track and record temperature and humidity levels per SOP guidelines., • Organize and maintain QA documentation., • Follow all company policies, safety protocols, cGMP standards, and SOPs., • 1–5 years of experience in QA within the pharmaceutical industry., • Strong understanding of GMP standards and regulatory requirements., • Experience with line inspections, document reviews, and batch record evaluations is a plus., • High school diploma required., • Ability to read and follow SOPs accurately. You’ll be based in a modern pharmaceutical manufacturing facility with multiple production lines. QA Inspectors typically oversee 1–3 lines at a time. Available shifts include: • 1st Shift: 7:00 AM – 3:30 PM, • 2nd Shift: 3:00 PM – 11:30 PM Pay and Benefits The pay range for this position is $38937.00 - $54080.00/yr. benefits start day 1 and they are eligible for 2 weeks vacation, 56 hours sick and wellness add 2 days mental health days Workplace Type This is a fully onsite position in Central Islip,NY. Application Deadline This position is anticipated to close on Sep 22, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionBenefits/Perks • Competitive Compensation PRIMARY RESPONSIBILITIES: Operate industrial equipment (e.g., forklift, pallet jack) to handle materials, including lifting up to 40 feet. Follow safety procedures and standard guidelines for assigned tasks. Check incoming shipments against documentation, counts items, and reports damaged items. Adhere to Good Manufacturing Practices (cGMP) and company Standard Operating Procedures (SOP), Additional duties as assigned.

Operators may be required to cross-train in all areas of the manufacturing operations. Job title-Manufacturing Operator (FBD, Granulation & Coating). Manufacturing and filling of products as per Batch Manufacturing Records and SOP.

Benefits: • 401(k), • 401(k) matching, • Dental insurance, • Employee discounts, • Health insurance, • Opportunity for advancement, • Paid time off, • Parental leave, • Signing bonus, • Training & development, • Tuition assistance, • Vision insurance Join the fastest growing Academy of Early Education in the nation where “Happy Happens Here”! At The Learning Experience, we are committed to giving everyone a platform to display their talents, share their ideas, and grow their careers in Early Childhood Education. As a Center Director, you’ll lead a passionate team and make a meaningful difference in the lives of children, their families, and your community. Compensation: $65 - $70,000/year What We Offer: • Competitive Benefits: Health, Vision, Dental Insurance, 401K, Pet Discount Plan, Childcare Discounts, and more!, • State-of-the-Art Classrooms: Lead in an immersive school and classroom setting utilizing the latest technology, materials, and resources to allow children to learn, play, and grow., • Prioritize recruiting and respond to applicants within 1 business day using tools like CareerPlug., • Ensure the center is fully staffed with well-trained, high-performing teachers using the onboarding SOP and celebrating milestone progress., • Create a team culture rooted in professionalism, kindness, and inclusion, aligned with TLE values and brand standards., • Conduct and document monthly team meetings focused on communication, recognition, and growth., • Deliver timely, constructive feedback and address performance issues promptly., • Keep employee turnover below 40% in a rolling 12-month period., • Complete and submit annual performance reviews using ADP, ensuring they are timely and properly filed., • Serve as the go-to for both staff and families—resolving concerns quickly, collaboratively, and respectfully. Enrollment • Execute a formal marketing plan that includes outreach, social media, events, and community engagement., • Lead and convert prospective families with warmth and professionalism—through both in-person and virtual tours., • Maintain strong lead-to-start conversion and consistently meet or exceed the center’s active enrollment budget., • Use systems to accurately forecast enrollment trends and make data-informed decisions., • Post engaging content on social media and solicit positive online reviews., • Conduct competitive shops 2x per year and use the insights to stay market-relevant., • Build strong relationships with families, ensuring high levels of satisfaction and retention. Profitability • Understand and manage your center’s monthly and quarterly budget targets, especially EBITDA., • Review and analyze your P&L to confirm financial performance and identify opportunities., • Maintain accurate billing records and manage tuition collection in line with due dates., • Monitor and manage center discounts responsibly., • Escalate any financial discrepancies promptly and professionally., • Support growth by contributing to enrollment targets and operational efficiency. Standards and Quality • Ensure health and safety SOPs are followed center-wide., • Maintain full compliance with all state and local licensing regulations., • Prioritize safe supervision practices, and ensure adherence to protocols around allergies, medications, and accommodations., • Keep the center clean, organized, safe, and always tour-ready., • Ensure student and staff files are accurate, up-to-date, and securely stored., • Leverage TLE tools, systems, and required platforms to optimize operations., • Replenish inventory on budget and as needed to maintain smooth center operations., • Process payroll on time and accurately., • Stay informed and responsive to labor laws, fire codes, health regulations, and internal policies., • Operate proactively, meet deadlines, and make sound decisions for your team, your center, and your business. Qualifications: • Two or more years of center management or people leadership experience highly preferred. At least one year required., • Must possess a state-specific Director or Administrative Credential and meet all licensing and background screening requirements., • Bachelor’s degree in Early Childhood Education or a related field is highly preferred., • Strong knowledge of early childhood education, licensing standards, and classroom best practices. #tlehp

Job DescriptionDescription: Position Summary: A Machine Operator is responsible for operating manufacturing machinery for compression/encapsulation in compliance with all regulatory SOP requirements and company policies. *Multiple Shifts Available - Day, Night, Weekend. Responsibilities: Including but not limited to - • Load and unload tablet press machines., • Monitor tablet press operation and report irregularities to management., • Follow all applicable safety rules, SOP’s and cGMP guidelines., • Exemplify superb ethical conduct, teamwork, integrity, respect and accountability., • Operator Level I: 6 months+ experience in pharmaceutical compression/encapsulation, • Operator Level II: 2+ years of work experience in pharmaceutical compression/encapsulation, • Strong mechanical aptitude, • Required to use hands/fingers to operate machinery, etc., • Must be able to lift up to 50 lbs and move 10-20 feet., • Must be able to stand, climb and bend for extended periods of time., • Indoor manufacturing environment including enclosed areas with dust and loud noises; close proximity to heavy machinery and pharmaceutical powders., • Potential to move between production operations sites/areas to complete job functions., • Operator I: $19.00 - $23.00 / hour, • Operator II: $20.50 - $24.50 / hour