Stock associate jobs in Boston, Massachusetts - Page 2Crear alertas

Job DescriptionCompany Description For over 164 years, Frette has crafted exquisite linens, blending Italian artistry with timeless luxury. Master artisans in Monza and Milan transform the finest fibers into creations of unmatched quality and elegance. Renowned for its signature finish, Frette has graced iconic destinations—from St. Peter’s Basilica to the Orient Express—while over 500 European royal families have slept beneath its sheets. Today, its legacy lives on in luxury hotels, private residences, yachts, and jets, remaining dedicated to outfitting the world’s most exceptional spaces. Job Description Frette is seeking a part time Support Associate for our boutique in Boston, MA. The Support Associate is an integral part of the store team, acting as a key partner to management and sales, primarily responsible for overseeing the stockroom and maintaining the upkeep of the store. At Frette we expect all employees to be team players by demonstrating a high degree of integrity and contributing to a positive environment that is fun, professional and productive. Employees are required to contribute to maintaining all brand and operating standards consistently while ensuring a high level of customer service through extensive product knowledge and commitment to an elevated selling ceremony. The Support Associate is responsible for Inventory Control, Client Experience, and Maintenance, as described below. INVENTORY CONTROL: • Inventory Control ownership including cycle counts, communicating adjustments, discrepancies, negative on hands, reports, informing store of new receipts, out of stocks, best sellers (on hand inventory levels), etc., • Execute all operational responsibilities to ensure the timely execution of all transfers, damages, fulfillments and holds, replenishment, shipping and receiving in order to maintain inventory accuracy and ideal product flow., • Ensure maximization and effectiveness of storage and capacity of all products to include front of house (sales floor), back of house and offsite storage locations., • Partner with the Store Manager and Sales Specialists to prioritize customer sales and ensure appropriate inventory levels and organization are maintained., • Ensure compliance of all operational policies and procedures are always met including but not limited to Loss Prevention, Inventory Control, Boutique Maintenance, Customer Capture, POS etc., • Follow Frette packaging guidelines for any ship outs, maintain a consistent company perspective and expectation on charge sends, returns/exchanges, and other such transactions that are critical to a positive customer experience., • Assist whenever necessary on the sales floor by providing floor coverage, supporting sales specialists and ensuring customer service standards are met., • Contribute to daily morning meetings with the store team. The focus of the day should be determined by the Store Manager in advance., • Participate in maintaining visual standards, including VM rotations, bed changes a daily standard., • Perform stockroom maintenance, stock checks, and shipping of product (transfers, customer related items, instore and E-comm fulfillments)., • Oversee ongoing facilities and maintenance in a timely and consistent manner including furniture repair, daily/monthly cleaning of stores (provide feedback to housekeeping services on quality of work on a daily basis), all repair work (walls, floors, fixtures, etc)., • Daily touch base with the Store Manager and team to outline priorities and align expectations., • In partnership with the Store Manager and Corporate Retail Team (Retail Coordinator, Director of Retail, Area Manager), manage and maintain annual budgets for the store's operational expenses (packaging, supplies, cleaning & maintenance, etc.)., • Perform key holder store opening and closing procedures as well as ensuring the opening/closing checklist has been completed and signed off on by the opening/closing associate., • A minimum of 3 years experience in a retail store environment, including back-of-house support., • Valid US driver’s license., • Flexibility to work a retail schedule which will include evenings, weekends, and holidays., • Must possess and consistently exhibit the competencies relative to the position., • Proficiency with retail operating systems including shipping, POS, Microsoft Office, and Google Workspace., • Detail-oriented, strong organization and follow-up skills., • Ability to multi-task and maintain organization in a fast-paced environment., • Self-motivated and ability to work well independently as well as within a team atmosphere., • Demonstrates a positive attitude that contributes to a positive team environment., • Team-oriented but also self-driven with an entrepreneurial spirit., • Ability to build and maintain effective working relationships with team members along with willingness to set and maintain high standards of performance., • Ability to travel as needed to off-site storage locations within a 15-mile radius., • Willingness to have a positive partnership with the Corporate team as well as other store teams., • Ability to lift and mobilize small to medium items up to 50 lbs. while utilizing appropriate equipment and techniques., • Ability to maneuver effectively around the boutique floor, stock room, and offsite., • Position entails prolonged standing, twisting, stooping, kneeling, squatting, bending and OSHA-approved ladder safety. Additional Information All your information will be kept confidential according to EEO guidelines. Pay rate for this role is $20 per hour. #LI-Onsite It is the policy and commitment of Frette to provide equal employment and advancement opportunities to all individuals. The objective of Frette is to recruit, hire, train, and promote the most qualified applicants into all job levels. Frette does not discriminate in employment opportunities or practices on the basis of race, color, religion, sex, sexual orientation, national origin, age disability, or any other characteristic protected by law. Frette will make reasonable accommodations for qualified individuals with known disabilities unless doing so would result in any undue hardship to the Company. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination, and access to benefits and training. For full time roles, in addition to the base salary, Frette offers a competitive benefits package that includes medical, dental, vision, life insurance, short + long term disability, 401K with Company match, paid maternity/paternity leave, employee discount, paid holidays, and a paid time-off policy.

Job Description We are seeking a reliable and hardworking Warehouse Associate to join our team at Katsiroubas Produce, a leading provider of fresh produce & specialty items in the Boston area. The ideal candidate will assist in maintaining an efficient and organized warehouse by performing tasks such as order picking, receiving deliveries, aisle rotation, inventory management, and ensuring the quality and freshness of products. If you’re detail-oriented, have a strong work ethic, and enjoy working in a fast-paced environment, we want to hear from you! Key Responsibilities: • Order Picking: Accurately pick and prepare orders based on customer or inventory requirements using handheld scanners or other technology., • Receiving & Stocking: Assist in the unloading of shipments, verifying product quantities, and checking for quality and freshness. Ensure all items are accurately logged into the inventory system and stored properly., • Aisle Rotation: Implement FIFO (First In, First Out) or FEFO (First Expired, First Out) practices to ensure the oldest stock is used first. Regularly check for any expired or damaged products and ensure proper disposal or return., • Inventory Management: Assist with inventory checks and stock audits, reporting discrepancies to supervisors. Help maintain accurate records of products and stock levels., • General Warehouse Maintenance: Ensure the warehouse environment is clean, safe, and organized. Assist with maintaining proper product placement to optimize space and efficiency., • Safety & Compliance: Adhere to safety standards and company policies, including the proper use of equipment such as forklifts, pallet jacks, and personal protective equipment (PPE)., • Team Collaboration: Work closely with other warehouse associates and supervisors to ensure smooth operations and timely order fulfillment., • Quality Control: Monitor the quality of the produce to ensure it meets company standards and customer expectations. Notify supervisors of any quality concerns immediately. Requirements: • High school diploma or equivalent preferred., • Previous experience in a warehouse or production environment, especially in produce handling, is a plus., • Ability to work in a physically demanding environment, including lifting, standing, and walking for long periods., • Strong attention to detail and ability to accurately follow instructions., • Knowledge of basic inventory and stock management systems is a plus., • Ability to operate warehouse equipment, such as forklifts, pallet jacks, and hand trucks (training may be provided)., • Strong communication and teamwork skills, bilingual in Spanish & English preferred., • Ability to work in a fast-paced, time-sensitive environment. Physical Requirements: • Must be able to lift up to 50 pounds regularly., • Ability to stand, walk, and bend for long periods of time., • Comfortable working in cold or refrigerated environments.Company DescriptionOur Mission We strive to build lasting partnerships with our customers by delivering the highest quality fruits, vegetables, and specialty products—tailored to meet their unique needs. Our Commitment Service and quality are at the heart of our fourth-generation family business. Through trusted relationships with some of the nation’s most established growers and farmers, we’re able to provide our customers with exceptional, fresh products. We proudly support local agriculture and are dedicated to offering sustainable solutions that benefit both our customers and our communities. As we look to the future, we remain committed to growing our business while honoring the legacy and values that have guided us for over a century.Our Mission\r\n\r\nWe strive to build lasting partnerships with our customers by delivering the highest quality fruits, vegetables, and specialty products—tailored to meet their unique needs.\r\n\r\nOur Commitment\r\nService and quality are at the heart of our fourth-generation family business. Through trusted relationships with some of the nation’s most established growers and farmers, we’re able to provide our customers with exceptional, fresh products. We proudly support local agriculture and are dedicated to offering sustainable solutions that benefit both our customers and our communities.\r\n\r\nAs we look to the future, we remain committed to growing our business while honoring the legacy and values that have guided us for over a century.

Job Description At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care). Position Summary: The Materials Associate I is responsible for shipping and receiving activities that include storage and transport of materials from suppliers, vendors and third-party warehouse to production areas. Schedule: As a company that thrives on teamwork and collaboration, this role will be required to work on-site 5 days a week. There are 2 Materials Associate I positions available. (1) Sunday - Thursday 8:00 - 4:30 and (2) Tuesday - Saturday 8:00 - 4:30. Position Scope: • Performs Manufacturing Support activities in accordance with established SOPs, cGMPs, and safety regulations., • Receives and distributes all Quality Controlled inspected and non-Quality Control inventoried material and general goods received at the Vericel site., • Loads and unloads delivery vehicles and assembles stock onto pallets, warehouse trucks, racks, bins, shelves, refrigerators, and freezers., • Opens cartons, bundles, and other containers and able to convey stock onto pallets, warehouse trucks, racks, bins, shelves refrigerators and freezers., • Stores, transfers, and distributes material in accordance with specific material requirements., • Maintains LN2 and CO2 systems including weekly manual fills of Liquid Nitrogen Cryovials Storage Dewars., • Assists with data entry of In-Transit requests for material from Third Party off-site storage location., • Maintains inventory control in ERP system by performing system transactions at time of material receipt, storage, and distribution., • Performs routine inventory cycle counts., • Participates in scheduled annual physical inventory activities., • Assists with Surgeon Training Kits order requests including preparation and sanitization of reusable material., • Prepares Vericel Biopsy Kit assemblies., • Performs Biopsy Accessioning activities (Receipt and Inspection) processes., • Assists with preparation of inventory sales order fulfillment and end of day closing activities., • Works with Materials Management and Accounting as needed to investigate and resolve receiving issues and coordination of material returns., • Maintenance of material staging areas., • Interacts with various groups (QA, R&D, QC, Materials Management, Sales and Marketing, Facilities & Engineering, Finance, Third Party Logistics, and Customer Care) on material requests and shipping and receiving activates., • GED, High school diploma or equivalent with a minimum of 1 years of experience working in a cGMP environment in the biotech or pharmaceutical industry., • Ability to comply with regulatory compliance within Vericel., • Experience in high volume and fast-paced materials and manufacturing support environment., • Excellent communication skills, written and verbal., • Experience operating motorized and non-motorized material handling equipment., • Organizational planning skills and the ability to collaborate with others in a team environment., • Experience with MS Office., • Knowledge of ERP inventory system Working Conditions & Physical Demands • May be required to work in classified and controlled areas such as clean room environment wearing special garments. Additionally, personal protective equipment must be worn due to safety requirements., • May be required to stand for long periods of time while performing physical duties., • May be required to lift, push or pull up to 40 lbs., • Must operate motorized and non-motorized material handling equipment., • Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care., • Career Growth: Be a part of a growing organization with opportunities to expand your impact The actual salary offered will be determined based on factors such as the candidate’s qualifications, experience, and skills. Bonus, incentive pay, equity and benefits may be provided in addition to the base compensation listed above. In accordance with Massachusetts law, Vericel provides the pay range that it reasonably and in good faith expects to pay for a particular and specific employment position at the time of posting or offer. This range is subject to change based on business needs, market conditions, and individual qualifications. Employees and applicants may request the pay range for their position or for a position to which they are applying. Retaliation for making such a request is strictly prohibited. EEO Statement All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer. Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

Job Description We're seeking a reliable and detail-oriented Warehouse Associate to join our growing distribution team. This role ensures accurate order fulfillment, inventory handling, and efficient warehouse operations. Key Responsibilities: • Receive, verify, and stock incoming shipments, • Pick and pack customer orders accurately, • Operate pallet jacks and hand trucks for material movement, • Maintain cleanliness and organization in the warehouse, • Perform routine inventory counts and report discrepancies, • Ability to lift up to 50 lbs regularly, • High school diploma or equivalent, • 1+ year of experience in a warehouse or distribution center, • Basic computer skills (for inventory tracking), • Strong attention to detail and teamwork By submitting my contact information to this job posting I agree to receive SMS messages from you about this submission and future opportunities. Standard data / text message rates may apply, and I can opt-out at any time by replying "STOP".

Job DescriptionEmerging Growth & Venture Capital Associate Attorney (Professional Track, 5–8 Years) Direct Counsel is seeking an Emerging Growth & Venture Capital Associate Attorney to join the corporate group of a leading global law firm as part of its Professional Track Attorney program. This position is open to candidates in all major U.S. offices, including Atlanta, Austin, Baltimore, Boston, Chicago, Dallas, Houston, Los Angeles, Miami, Minneapolis, New York, Palo Alto, Philadelphia, Phoenix, Raleigh, Reston, San Diego, San Francisco, Seattle, Short Hills, Washington, D.C., Wilmington, and Northfield. Role Focus The attorney will work with emerging growth companies and the institutional investors that support them, handling venture capital financings, M&A transactions, and a range of ongoing corporate governance matters. Experience Requirements Candidates should have 5 to 8 years of experience in emerging growth and venture capital work, including: * Preferred stock financings, bridge financings, and SAFE financings * Venture capital transactions using NVCA, Series Seed, and Y Combinator forms * M&A deal support and due diligence * Day-to-day governance for early-stage and high-growth companies Am Law 100 experience is preferred. Qualifications * JD from an accredited law school * Admission to practice in the relevant jurisdiction * Strong drafting, analytical, and communication skills * Ability to manage transactions and collaborate with teams * Excellent judgment, attention to detail, and client service orientation Compensation & Benefits * Expected salary range: $150,000 – $300,000, based on market, experience, and qualifications * Comprehensive benefits including medical, dental, vision, 401(k), and hybrid work flexibility Work Environment The position offers a hybrid schedule with regular in-office presence and opportunities to work collaboratively while maintaining flexibility. The role also includes opportunities to supervise junior team members and engage in a supportive, growth-oriented environment. This is a strong opportunity for a mid- to senior-level associate attorney seeking to focus on emerging companies, venture capital transactions, and related corporate work within a structured professional track model.

Job Description Job Title: Manufacturing Associate – Cell Therapy Production Job Description We’re seeking a Manufacturing Associate to join our growing team focused on the production of T cell and TCR-engineered therapies. This role is ideal for someone with strong GMP experience, a proactive mindset, and a commitment to quality and safety in a cleanroom environment. Responsibilities • Operate production equipment and perform processing steps in compliance with GMP standards., • Accurately complete production documentation and batch records., • Maintain cleanliness and organization of the production area., • Stock and manage supplies to ensure uninterrupted operations., • Troubleshoot equipment and process issues to maintain operational efficiency., • Support or lead Commissioning and Validation activities., • Assist in the creation and revision of manufacturing documentation., • Identify and implement continuous improvement opportunities., • Ensure compliance with cGMP, safety protocols, and regulatory requirements., • Associate’s or Bachelor’s degree in a scientific or related field., • 5+ years of experience in cleanroom or GMP manufacturing environments., • Hands-on knowledge of T cell therapy and TCR-engineered cell therapies, with a minimum of 2-3 years of experience., • Experience with both upstream and downstream manufacturing., • Strong understanding of GMP, batch record review, and biologics production., • Experience with controlled document creation and review., • Excellent documentation and communication skills., • Proficiency in Microsoft Word, Excel, Outlook, and PowerPoint., • Must be able to read, write and speak English fluently., • Ability to lift and transport packages weighing up to 50 pounds., • Extensive walking throughout the facility will be required. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Waltham,MA. Application Deadline This position is anticipated to close on Feb 6, 2026. 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 Description Full Time Shift: 5:00am-1:30pm with every other weekend rotating holidays Pay Range: $18.00-$20.00 Based on experience with Mileage reimbursement ROLE: The Mobile Phlebotomist, under the general supervision of the Phlebotomy Supervisor, works to provide clinical pre-analytical laboratory services to our clients/patients in a mobile setting. They are responsible for completing their assigned routes in a safe and timely manner. They must follow all policies and procedures. TASKS AND RESPONSIBILITIES: • Drives vehicle to client facilities, typically nursing homes, as directed by company dispatcher., • Unloads phlebotomy tray and takes to patient’s bedside to collect samples ordered by physician., • Accurately identifies patient after collecting specimen(s)., • Accurately collects, labels, processes, and delivers specimens obtained from patients., • Reloads equipment and all necessary specimens to vehicle for prompt delivery., • Regularly communicates with dispatcher to report status and location., • Strict adherence to Universal Precautions in controlling blood-borne pathogens and infectious disease exposures., • Maintain required certifications, health requirements, and operational requirements., • Keeps work area clean., • Follow all required safety precautions ALL the time., • Reports any unsafe conditions in the workplace., • Reports all complaints and problems encountered., • Monitors supplies inventory., • Reports low stock or out-of-stock situations., • Identifies and segregates any expired supplies, • Reports to work promptly, properly groomed and wears the proper identification at all times when visiting a facility., • Accurately maintains time records of hours worked and deliver to company as directed. Manages his/her assigned shift to include meal breaks. • Follows all specimen preservation, patient preparation and specimen management processes and procedures as written without personal deviation, • Drives vehicle to client facilities (mostly nursing homes), as directed by company dispatcher or assigned supervisor or coordinator., • Unloads phlebotomy tray provided by the company and takes to patient’s bedside to collect samples for tests ordered by physician., • Accurately identifies patients after collecting specimens., • Accurately collects, labels, processes and delivers specimens obtained from patients., • Reloads equipment and all necessary specimens to vehicle for prompt delivery., • Regularly communicates with dispatcher to report status and location. Creates all required records per instructions., • Follows all specimen preservation, patient preparation and specimen management processes and procedures as written without personal deviation, • Uses only approved current documents. • Makes changes to records ONLY per approved instructions as needed; • Practices excellent communication and interaction skills specific to the population served, including the pediatric and geriatric communities., • Treats customers and patients with respect, dignity, and discretion; acknowledging residents’ rights and patients’ right to refuse, • Demonstrate regular attendance, • Must have a current, valid State phlebotomy license (if required), • Must have a current, valid State Driver’s license; car insurance; good driving record; a possess a vehicle in good working condition suitable to meet daily driving requirements, • Proficient in venipuncture and skin puncture using both vacutainer and syringe techniques, • Knowledge of laboratory operations, • Maintains sterile, sanitary conditions to prevent contamination PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to walk, stand, handle or feel, talk and hear. The employee is occasionally required to sit, reach with hands and arms, stoop, kneel, crouch, or crawl. The employee may lift and or move up to 35 pounds on occasion. Specific vision abilities required by this job include close vision, depth perception, and the ability to adjust focus. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an Associate may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The standard medical laboratory environment is one in which potential health hazards do exist. Administrative, technical and professional staff is expected to safely operate in accordance with applicable and appropriate health and safety policies and procedures, as prescribed by the Environmental Health and Safety Manual. This includes consistent and proper use of Personal Protective Equipment. Associates work in all weather and driving conditions.

Job DescriptionCompany Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview Reporting to the Associate Director, Cybersecurity, Rhythm is seeking an experienced and highly motivated Senior Cybersecurity Specialist to join the Information Technology team. This role will be responsible for supporting cybersecurity initiatives in governance and compliance, risk management, vulnerability management, and incident response. As a senior member of our cybersecurity team, you will leverage risk-based assessments and industry-specific threat intelligence to strengthen Rhythm’s security posture and participate in routine incident response activities. You will also play a pivotal role in enhancing security awareness and education across all business units. Responsibilities and Duties • Identify and escalate cybersecurity risks related to Rhythm’s systems, data, and third-party relationships and drive timely remediation efforts, • Execute the vulnerability management program, ensuring vulnerabilities are addressed within defined SLAs, • Serve with others as a first responder during security incidents, performing detailed technical analysis and coordinating response activities, • Support threat hunting and digital forensics initiatives to uncover threats and assess overall risk exposure, • Partner with cross-functional teams on projects impacting confidentiality, integrity, or availability of critical assets, • Review and validate security requirements within third-party contracts, including data protection clauses, breach notification obligations, and compliance with relevant regulations, • Conduct thorough third-party data security assessments to evaluate controls, risk posture, and alignment with organizational standards, • Provide and maintain general cybersecurity training and education for all Rhythm employees, • Maintain clear, accurate, and up-to-date documentation for cybersecurity policies, procedures, and standards. Ensure incident response playbooks, vulnerability management workflows, and system hardening guides are well-documented and easily accessible, • Minimum 5 years of experience in cybersecurity disciplines such as governance and compliance, risk management, vulnerability management, cloud security, and incident response, • Hands-on expertise with platforms including Microsoft Defender, CrowdStrike, Azure, and AWS, • Strong knowledge and application of the CIS Controls and NIST Cybersecurity Framework., • Familiarity with regulatory and compliance standards (e.g., NIST, GDPR, ISO, SOC 2)., • Proven ability to manage the full security incident response lifecycle: detection, analysis, containment, eradication and recovery., • Demonstrated success in project management within collaborative environments, • Excellent communication and interpersonal skills (written and verbal) This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs. This role may involve some travel. The expected salary range for this position is $90,000-$135,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units. More about Rhythm We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. At Rhythm our core values are: • We are committed to advancing scientific understanding to improve patients’ lives, • We are inspired to tackle tough challenges and have the courage to ask bold questions, • We are eager to learn and adapt, • We believe collaboration and ownership are foundational for our success Headquartered in Boston, Rhythm is proud to have been named one of the Top Places to Work in Massachusetts. Powered by JazzHR gF6za1n2ls

Job Description Equity Research Associate to help cover the Biotechnology sector. This person will be responsible for following the progress of public/private Biotechnology companies and will support the research team in its efforts to analyze companies and make stock recommendations to institutional investor clients. In addition to a background in the life sciences, the ideal candidate will have a passion for stocks, interest in equity research and financial modeling, specifically in the Biotechnology sectors with a focus on oncology. The position is located in Boston, MA. Essential Job Functions · Provide support to the Senior Analyst through fundamental analysis and investment research in equity markets with an emphasis on original, bottom-up research in the Biotechnology sector · Analyze individual Biotechnology companies to build and update fully integrated financial and valuation models · Write comprehensive research reports and present findings; draft reports/notes on relevant investment themes, events and breaking news · Conduct primary research through industry sources including, but not limited to, financial analysis, due diligence clinical data and industry trends, company management and strategies · Organize physician calls for investors and investor events · Update analyst marketing handout regularly · Interact with Firm’s institutional sales force and investor clients · Respond to client and internal inquiries regarding research findings and directives Preferred Qualifications · MD, PhD., or other advanced life sciences degree · 1-3 years of professional industry experience in industry, consulting, or similar · Exceptional analytical, verbal, and written communication skills · Analytical mindset, intellectual curiosity, aptitude for math/statistics Basic Qualifications · Bachelor’s degree required · Ability to search, understand and interpret scientific and medical publications and presentations Work Location · Currently, this role is expected to be in the Boston office at least 4 days per week. Salary · Annual base salary between $140,000 and $165,000. · The base salary range represents the low and high end of the anticipated base salary range for this position. Actual base salaries may vary depending on factors such as location and experience. The range listed reflects base salary only, and the total compensation package may include other components such as incentive compensation.

Job Description Blufox Mobile is hiring Sales Representatives, and we want you to join our team today! We offer aggressive hourly pay plus a rich commission. Our reps can make $18-35 per hour. Our entrepreneurial and innovative work culture ensures limitless opportunities for growth within the company and our excellent training program positions you well to be a successful contributor to this essential business. Who we are: Blufox is a fast-growing branded partner for Comcast XFINITY services with locations in 15 states and rapidly expanding. Under the XFINITY brand, Comcast is one of the nation's largest High-speed Internet, MOBILE, Home Security, Video and Voice providers to residential and business customers. As a preferred branded partner, Blufox has seen extensive growth and is poised to expand its retail footprint to over 200 locations across the US in the coming years. What we are looking for: The ideal candidate is someone with retail rales experience and eager to be a part of our growing team! Experience selling Mobile and Cable products is a huge plus. As a Sales Rep your primary duties will be promoting the sale of all Xfinity services and products – Internet, Mobile, Video, Home Security and Voice. You will develop a foundational knowledge of Comcast products and services, utilize sales skills, and learn to maximize sales through effective upselling while maintaining a positive customer experience. Benefits include: · Medical, Dental, Vision, 401k · Paid training · Opportunities for promotion- We have several managers who have been promoted from within. · Blufox ESOP- Employee Stock Ownership Program (* for select stores) This provides employees and opportunity to own a part of the company they work for as a reward for loyalty and performance. · Exclusive employee growth and reward programs: Automatic compensation increases through “Blufox Raise Program”. This allows front line employees to earn multiple raises per year. You can influence the increases you get by the work you do. Take charge of your own destiny and never feel like you need to have uncomfortable conversations about pay increases. Blufox “Milestone Program” provides employees rewards and recognition every time they hit required sales objectives. “Level Up” from Sales Associate to Lead Sales Associate to Senior Lead purely on the basis of your performance. Annual “Blufox Winners Circle” trip to Mexico. Top Reps, Managers and DMs get an all-expenses paid trip to Mexico at an upscale resort where you can celebrate your successes with other winners and company leadership. *Ask your interviewer about these unique employee-focused programs. Core responsibilities: Sales Do you use internet, mobile, cable, voice or home security products? Then you are already familiar with what you have to sell. · Present, promote and sell these products/services using effective knowledge to existing and prospective customers. Sell additional services by recognizing opportunities and articulating our competitive advantage to up-sell accounts, explaining new features. · Execute sales closing techniques consistently, repeatedly, and in a timely manner to maximize your Gross Profit. · Create value around all our products and services and tailor a package to fit our customer's needs. · Meet and exceed sales targets consistently and maximize your own commissions. Customer service · Maintain a courteous and friendly attitude when interacting with customers in a constantly changing environment. · Build a positive work relationship with customers to enhance the image and public perception of a company. · Strive to achieve the maximum Net Promoter Scores (NPS) with each customer interaction. Organization goals · Work well with the team, have relationship management skills and openness to feedback. · Stay up to date with current and emerging communications and entertainment technologies for both the Company and its competition. · Achieve overall performance goals of the organization. · Regular, consistent, and punctual attendance. Must be able to work nights and weekends, variable schedule(s), and overtime, as necessary. Job Qualifications · Wireless/Cable/Retail sales experience preferred · High school degree or GED · Ability to stand for long periods of time · Ability to lift objects weighing up to 25lbs · Reliable transportation · Full Time, Open Availability Job Types: Full-time, Commission Pay: $35,000.00 - $65,000 per year

Job Description Pharmacovigilance Operations Associate Director – Solid Biosciences Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care. Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases. We are seeking an Pharmacovigilance Operations Associate Director to support and execute global pharmacovigilance operational activities across Solid’s clinical development programs. This role will focus on day-to-day PV operations execution, vendor oversight, and cross-functional coordination. This position will play a key role in ensuring timely and compliant safety operations in support of Solid’s growing gene therapy pipeline This role will report to Sr. Director, Pharmacovigilance Sciences and will be based in Solid’s Corporate Headquarters located in Hood Park in Charlestown, MA or remote/ hybrid depending on candidate location and business needs. Key Position Responsibilities • Execute global pharmacovigilance operational activities for Solid’s clinical-stage gene therapy programs under the direction of PV leadership., • Oversee day-to-day PV operations, including:, • Case processing oversight for SAEs and AESIs, • Compliance monitoring for expedited safety reporting (SUSARs) to global health authorities, • Operational support for periodic safety reports (DSURs, IND Annual Reports, 6-month line listings), • Serve as the primary operational contact for outsourced PV vendors, supporting:, • Day-to-day vendor oversight and issue resolution, • Oversight of PV-related SOWs, Safety Management Plans, • Monitoring of vendor performance against defined KPIs and SOWs, • Support the migration of safety cases to a new safety database, including coordination with vendors, support of data reconciliation activities, and documentation review under established plans., • Support the development, maintenance, and implementation of PV SOPs, work instructions, and operational processes., • Partner with Clinical Operations, Clinical Development, Regulatory Affairs, Quality, and Biometrics to ensure accurate and timely safety data flow., • Provide operational support for safety governance activities, including:, • Safety Management Committees (SMCs), • DSMB/DMC interactions, as applicable, • Support inspection and audit readiness activities, including document preparation, response drafting, and participation in mock inspections., • Assist in tracking and implementing updates related to evolving global PV regulations and guidance., • Provide day-to-day guidance and oversight to other PV staff or contractors, as applicable Experience Requirements • Bachelor’s degree in a life science or healthcare-related field is required; an advanced degree (PharmD, MPH, RN) is preferred., • Minimum of 3–5 years of pharmacovigilance experience, with hands-on experience managing clinical-stage PV operations, preferably within rare disease and/or gene therapy programs., • Experience supporting Phase 3 clinical trials, including blinded study designs and management of safety operations in compliance with blinding and unblinding procedures, is a plus, • Strong working knowledge of global PV regulations and guidance, including:, • FDA (21 CFR 312, IND safety reporting), • EMA (GVP Modules), • ICH guidelines (E2A–E2F), • Demonstrated experience overseeing PV vendors and outsourced models., • Experience supporting regulatory inspections and audits., • Familiarity with safety databases (e.g., Argus, ArisG) and EDC-to-safety data reconciliation processes. Key Position Attributes • Strategic and operational mindset with the ability to “roll up sleeves” in a fast-paced biotech environment., • Strong attention to detail with a high level of accountability and ownership., • Excellent cross-functional communication and collaboration skills., • Ability to interpret and operationalize regulatory guidance into practical, compliant processes., • Comfort operating in ambiguity and contributing to the build-out of new systems and processes., • Patient-focused perspective with an appreciation for the unique safety considerations of gene therapy and rare diseases., • Proven ability to prioritize, manage competing deadlines, and influence without authority. Compensation The base compensation range for this role is: $200,000 to $230,000 Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid’s long term company performance. Benefits and Solid Advantages At Solid Biosciences we offer a highly competitive total rewards and benefits package, intended to support all aspects of our employees’ lives and well-being. Additionally, for those employees working onsite at our Hood Park Headquarters, we offer a variety of onsite resources to support those working in our offices. • Competitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs, • 401(k) program participation with competitive company matched contributions, • Eligibility to participate in Solid’s Employee Stock Purchase Plan, • Mobile phone subsidy for eligible employees, • Tuition Reimbursement, • Vision Coverage, • Life Insurance, • Voluntary Pet Insurance, • Employee Discount Program on Travel, Entertainment, and Services, • Daily Subsidized Lunch Delivery (onsite @ Hood Park), • Free Onsite Full-Service Gym (onsite @ Hood Park), • Employee Parking (onsite @ Hood Park)

Job DescriptionCompany Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview The Associate Director (AD) of Regulatory Operations is responsible for assisting the Head of Regulatory Operations in maintaining Rhythm’s regulatory submission standards and current electronic submission guidelines/requirements. This role involves managing the preparation of eCTD submission-ready documents, coordinating across functions, and ensuring quality, accuracy, and adherence to regulatory guidelines. Additionally, the Associate Director supports the preparation and submission of Investigational New Drug applications (INDs), New Drug applications (NDAs), annual reports, Development Safety Update Reports (DSURs), and safety reports to regulatory authorities. Responsibilities and Duties • Manage regulatory operations activities, ensuring timely and accurate regulatory submissions, and collaborating with cross-functional teams for our US, EU, UK and Health Canada regions, • Identify/address opportunities to enhance operational effectiveness and drive process improvements within the department, • Manage regulatory operations activities, including preparation of eCTD submission-ready documents, coordination across functions, and adherence to regulatory guidelines and processes, • Support development program projects by collaborating with multi-disciplinary project teams to ensure successful program deliverables, • Assist in the development of Standard Operating Procedures (SOPs) quality assurance, and records management practices related to regulatory operations activities, • Track regulatory department information such as commitments with health authorities and NDA/IND commitments, • Act as an expert resource for eCTD submissions to FDA, ensuring compliance with internal and health authority standards, • Support the development and maintenance of operations resources for submission documents, • Identify new or revised regulatory policies and initiate activities to support compliance, • Bachelor’s degree in life/physical sciences or related field, • 8+ years of highly relevant pharmaceutical/biotechnology experience in Regulatory Affairs Operations, • Knowledge and understanding of the drug development process, • Strong knowledge of FDA and Global EU/UK regulations and guidelines, especially CTD and eCTD structure, • Experience with Veeva RIM EDMS, • Highly proficient in Microsoft Office suite, • Ability to balance both strategic and operational approaches, “think outside the box” and to manage multiple tasks in a fast-paced environment, • Detail-oriented and highly organized The expected salary range for this position is $160,000 - $240,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units. More about Rhythm We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. At Rhythm our core values are: • We are committed to advancing scientific understanding to improve patients’ lives, • We are inspired to tackle tough challenges and have the courage to ask bold questions, • We are eager to learn and adapt, • We believe collaboration and ownership are foundational for our success Headquartered in Boston, Rhythm is proud to have been named one of the Top Places to Work in Massachusetts. Powered by JazzHR jAJdEe3L2U

Job Description Process Sciences Drug Product Associate Director – Solid Biosciences Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care. Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases. We are seeking an experienced and highly motivated candidate to lead Drug Product activities within the newly formed Process Sciences Department within Solid Bio’s Technical Operations team. Through your deep product and process understanding you will shape CMC and program strategy and ensure robust control strategies to the benefit of patients worldwide. In this role, you will be a key subject matter expert across one or more areas of drug product sciences including formulation development, primary container development, fill-finish process development, optimization, and scale-up, and Product Validation studies. This is a highly cross-functional role that will work closely with Drug Substance process sciences, MSAT, analytical sciences & QC, device development, supply chain management, Regulatory, and Quality in CMC teams to drive technical and strategic decision-making This role will report to Director – Process Sciences and will be a remote or hybrid position. Up to 15% travel will be required at times. Key Position Responsibilities • Serve as a liaison to CMC teams to shepherd new pipeline products from development into manufacturing providing technical expertise across formulation, container/closure systems, fill‑finish, scale‑up, and product validation for gene therapy programs., • Partner with Technical Operations and CMC leadership as a Drug Product SME to define integrated strategies that support regulatory alignment, patient needs, and long‑term commercial readiness., • Lead the implementation of phase appropriate drug product process control strategies by following the FDA guidance and QbD to enable effective validation strategies at external CDMOs., • Ensure readiness for clinical and commercial manufacturing through risk‑based process understanding, comparability, and lifecycle management., • Partner with Analytical Development to analyze, and interpret drug product characterization, stability, and release data while defining CQAs for Drug product processes., • Provide technical expertise to pre-validation risk assessments using risk management tools. Work collaboratively and cross functionally to help ensure that process risks are analyzed, appropriately controlled and appropriately documented., • Provide technical expertise for establishing critical process parameters and a process validation strategy that supports product licensure including design and oversight of process characterization activities ensuring robust operational range finding studies and establishment of appropriate NORs and PARs for in process controls., • Design and execute product validation studies, (Ex: Time out of Refrigeration, container closure integrity (CCI), and leachable and extractable studies)., • Lead selection and development of container closure systems that support drug product and delivery requirements while ensuring quality, stability, manufacturability, and scalability across clinical and commercial supply., • Lead or support container closure integrity (CCI) testing across development, validation, and commercial manufacturing in alignment with regulatory expectations., • Drive selection and integration of drug delivery devices in collaboration with clinical and regulatory functions., • Design and execute container closure and delivery system qualification and in‑use compatibility studies, including evaluation of material interactions, adsorption, and extractables/leachables across manufacturing, storage, handling, and administration conditions., • Lead phase‑appropriate drug product formulation development, characterization, and design space definition through risk‑based screening, optimization, and robustness studies., • Characterize and evaluate formulations by assessing critical quality attributes (e.g., potency, purity, stability, particulates, aggregation) under relevant manufacturing, storage, and in‑use conditions., • Assess formulation performance and stability across manufacturing operations and lifecycle stages, including preparation, sterile filtration, filling, freezing/thawing, storage, and stress conditions., • Support lifecycle management activities, including formulation changes, comparability assessments, and continuous improvement initiatives., • Lead or significantly contribute to Drug Product sections of regulatory submissions (INDs, BLAs/MAAs), health authority responses, and inspection readiness activities related to drug product., • Author and review regulatory submissions: IND/IMPD, briefing books and BLA., • Serve as a subject matter expert in regulatory agency interactions, audits, and inspections. Experience Requirements • Bachelor’s degree in science, engineering or equivalent with 12+ years of experience working in a related pharmaceutical environment. Advanced degree (MS/PhD) preferred., • Deep knowledge of drug product process development and pharmaceutical manufacturing for biologics and/or Advanced Therapies including Fill‑finish and aseptic processing knowledge, including formulation preparation, sterile filtration, aseptic filling, frozen storage, and handling considerations., • First-hand experience in successfully scaling up and executing drug product manufacturing processes on pilot plant and/or commercial manufacturing scales across all phases of drug development from initial regulatory filings through registration, validation and launch., • Demonstrated experience with multiple aspects of Drug Product manufacturing including drug product formulation, fill/finish processes, clinical in-use studies and product image (container, volume, etc.) design., • Strong understanding of critical quality attributes (CQAs), critical process parameters (CPPs), and critical material attributes (CMAs) for drug product processes., • Experience supporting regulatory submissions (IND, BLA/MAA) with respect to drug product, formulation, CCS, and validation sections., • Knowledge and experience working in accordance with cGMP, GDP, GCP, and ICH guidelines including Quality by Design (QbD) and risk‑based development principles (ICH Q8(QR), Q9, Q10). Key Position Attributes • Proven ability to work effectively across Technical Operations, Drug Substance, MSAT, Analytical Sciences, Quality, Regulatory, Device Development, and Supply Chain., • Strong interpersonal flexibility with ability to adapt to other personalities in a respectful manner that is conducive to the achievement of personal and team goals., • Excellent communication skills, both oral and written, which may include planning and execution of meetings and presentations., • Ability to multitask and handle multiple competing priorities and projects at once in a changing and fast-paced environment., • Experience engaging with external suppliers and partners including contract manufacturing organizations., • Expertise in comparability assessments, post‑change risk evaluations, and lifecycle management., • High attention to detail with the ability to operate effectively at both strategic and execution levels., • Scientific curiosity paired with pragmatic decision‑making. Compensation The base compensation range for this role is: $180,000 - $220,000 Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid’s long term company performance. Benefits and Solid Advantages At Solid Biosciences we offer a highly competitive total rewards and benefits package, intended to support all aspects of our employees’ lives and well-being. Additionally, for those employees working onsite at our Hood Park Headquarters, we offer a variety of onsite resources to support those working in our offices. • Competitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs, • 401(k) program participation with competitive company matched contributions, • Eligibility to participate in Solid’s Employee Stock Purchase Plan, • Mobile phone subsidy for eligible employees, • Tuition Reimbursement, • Vision Coverage, • Life Insurance, • Voluntary Pet Insurance, • Employee Discount Program on Travel, Entertainment, and Services, • Daily Subsidized Lunch Delivery (onsite @ Hood Park), • Free Onsite Full-Service Gym (onsite @ Hood Park), • Employee Parking (onsite @ Hood Park)

Job DescriptionDescription: Function: Reporting to the Radiology Supervisor, the Radiology/Mammography Technologist will perform all digital x-ray and mammography examinations as assigned. This individual will have the working knowledge of all facets of digital x-ray and mammography. Representative Duties: Performs X-rays and screening mammogram studies as assigned • Greet each client with a smile and welcoming, professional manner, • Calls patients from the lobby into the exam room, • Disinfects exam rooms daily and after contamination of communicable disease exposure with appropriate cleaning agent, or insures that this is done, • Stocks exam rooms with supplies and equipment, • Maintains equipment in good working order, • Alerts Radiology Supervisor of broken equipment, • Confirms demographic information before conducting exam or scan; accurately record and enter any changes received, • Abides by recognized ALARA & HIPAA requirements, • Demonstrates a commitment to customer services, • Assists in training other employees in the medical support department, • Remains familiar with emergency procedures and codes, • Receives and places necessary telephone calls consistent with professional matters and clinic business, • Demonstrates competency in alphabetizing, filing, faxing and other duties to support administrative office needs, • Suggests and participates in continuing quality improvement efforts, • Adheres to all agency and departmental policies and procedures, • Participates in quality assessment and improvement activities as requested, • Adheres to the highest principles of patient and client confidentiality, • Adheres to established safety policies, procedures and precautions; identifies potential or actual unsafe situations in the environment and takes measures to rectify the situation, • Attends all required meetings, in-services and professional trainings, • Attends all regularly scheduled research meetings, trainings, forums and pertinent FCH staff meetings, • Maintains professional competence necessary to perform job responsibilities; maintains and provides agency with records of continuing education activities, • License/Certifications: Massachusetts RT license, Massachusetts Mammography License, current standing with ARRT, BLS certification, • Education: Associate degree in Radiologic Technology with certification in mammography, • Maintains CEU accreditation as needed for licensure, • Demonstrates competency in EMR, Microsoft Outlook, • Ability to work as part of a multidisciplinary team, • Experience working with an ethnically, culturally, and racially diverse environment, • Ability to work harmoniously and effectively with colleagues, patients, clients and vendors across the spectrum of diversity, including but not limited to race, ethnicity, color, gender identity, sexual orientation, age, socio-economic status, national origin and immigrant status, religious or spiritual identity, disability (physical, mental, emotional and developmental), veteran status, and/or limited English proficiency., • Minimum 2 years’ experience, • Experience with patients with HIV and electronic medical records, • OSHA category 1, • Physical Requirements: regularly required – sitting; using hands to manipulate objects/tools/controls; reaching with hands and arms; standing and adjusting patient positioning; talking; hearing; occasional lifting required up to 25 lbs., • Noise level: usually quiet LGBTQIA+ identified persons, Black, Indigenous, and other people of color (BIPOC), and individuals from other historically underrepresented communities are strongly encouraged to apply. This is a union position in a Fenway Health bargaining unit represented by 1199 SEIU United Healthcare Workers East.

Job DescriptionAbout UsDeep Genomics is at the forefront of integrating artificial intelligence and complex biology to transform drug discovery. Our proprietary machine learning platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, bioinformatics, data science, genetics, chemistry and drug development, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how medicines are created. About the RoleWe are seeking a highly motivated Senior Research Associate to join our Platform Technology team and play a critical role in advancing our AI-enabled RNA therapeutics discovery platform. In this position, you will design, implement, and optimize genomics-based assays that power therapeutic discovery, screening, and validation across a wide range of cellular systems. You will support high-throughput evaluation of novel RNA therapeutics—including modalities such as ADAR editing, ASOs, siRNAs, and mRNAs—and generate high-quality molecular data that directly feeds into computational models and therapeutic decision-making. As a key contributor within a dynamic research environment, you will collaborate closely with computational scientists, platform biologists, and therapeutic program teams. You will develop and execute next-generation sequencing assays, functional genomics readouts, and high-throughput molecular screens that drive target validation, lead optimization, and drug profiling. This role is ideal for candidates who thrive in a fast-paced, cross-functional setting and enjoy building and scaling cutting-edge experimental technologies.Key Responsibilities • Design, execute, and optimize high-throughput genomics assays, including NGS workflows, targeted sequencing, RNA-seq, and high-content gene expression readouts, to evaluate RNA therapeutic candidates., • Sequence prepared libraries independently using instruments such as the Illumina NextSeq, including run setup, instrument operation, and routine troubleshooting., • Troubleshoot library prep, QC metrics, and workflow bottlenecks to ensure consistently high-quality datasets for computational analysis., • Implement automated workflows using liquid handlers (e.g., Hamilton STAR, Agilent Bravo, Beckman Echo) to scale discovery and screening activities., • Perform a broad range of molecular biology techniques including PCR, qPCR/ddPCR, and nucleic acid extractions on a variety of cell types and tissues., • Clearly document experimental plans, results, SOPs, troubleshooting steps, and data within an electronic lab notebook (ELN)., • Present experimental findings and assay performance updates to project teams and collaborators.Basic Qualifications, • BS or MS in Molecular Biology, Genetics, Genomics, Biotechnology, Biochemistry, or related discipline with 3–6 years of relevant industry experience., • Strong understanding of molecular and cell biology principles., • Experience with NGS library preparation, including amplicon-seq, bulk RNA-seq, targeted panels, or single-cell sequencing., • Experience extracting RNA/DNA from cells and animal tissues., • Demonstrated proficiency in designing and executing genomics-based or molecular assays., • Excellent communication, organizational, and documentation skills., • Ability to prioritize and drive work independently in a fast-paced research environment.Preferred Qualifications, • Proficiency with specific liquid handling platforms such as Hamilton STAR, Agilent Bravo, or Beckman Echo., • Familiarity with RNA therapeutic modalities (ADAR editing, ASOs, siRNAs, mRNA)., • Hands-on experience growing, maintaining, and transfecting mammalian cells., • Prior experience in a biotechnology, pharmaceutical, or platform-driven discovery environment and demonstrated ability to collaborate within a highly cross-functional and multidisciplinary team.What we offer, • A collaborative and innovative environment at the frontier of computational biology, machine learning, and drug discovery., • Highly competitive compensation, including meaningful stock ownership., • Comprehensive benefits - including health, vision, and dental coverage for employees and families, employee and family assistance program., • Flexible work environment - including flexible hours, extended long weekends, holiday shutdown, unlimited personal days., • Maternity and parental leave top-up coverage, as well as new parent paid time off., • Focus on learning and growth for all employees - learning and development budget & lunch and learns.

Job DescriptionCompany Description Are you ready to trade your job for a journey? Become a FlyMate! Passion, excitement & global collaboration are all core to what it means to be a FlyMate. At Flywire, we’re on a mission to deliver the world’s most important and complex payments. We use our Flywire Advantage - the combination of our next-gen payments platform, proprietary payment network and vertical specific software, to help our clients get paid, and help their customers pay with ease - no matter where they are in the world. What more do we need to truly be unstoppable? Perhaps, that is you! Who we are: Flywire is a global payments enablement and software company, founded more than a decade ago to solve high-stakes, high-value payments in higher education. We’ve since scaled into new regions and industry verticals and expanded our product offerings to deliver meaningful value to our clients around the world. Today we support more than 4,800 clients across the global education, healthcare, travel & B2B industries, with diverse payment methods across 240 countries & territories and more than 140 currencies. With over 1,200 global FlyMates, representing more than 40 nationalities, and in 12 offices world-wide, we’re looking for FlyMates to join the next stage of our journey as we continue to grow. Job Description The Opportunity: As a Client Success Operations Associate, you will be the first line of support for our hospitality and e-commerce customers. This role focuses on solving routine issues, documenting findings, and delivering empathetic, professional communication to customers. • Weekend coverage is required (Saturdays and Sundays), with two weekdays off (preferred days off not Monday or Friday). Please only apply if you are able to provide weekend coverage, • Respond to a high volume of customer tickets, calls, and emails with empathy, professionalism, and efficiency., • Troubleshoot technical issues using logs, developer tools, DataDog, and internal tools., • Provide clear replication steps, screen recordings, or documentation to escalate issues to Engineering., • Translate technical findings into simple, actionable updates for customers and internal stakeholders., • Assist in writing SOPs and contributing to knowledge base articles and internal documentation., • Take ownership of escalated or pattern-based tickets and track them to resolution., • Identify bugs or process inefficiencies and work with the team to improve the support workflow., • Support common use cases such as PDF conversion and basic platform navigation., • Maintain quality responses while averaging ~25 solved tickets per day (≈575–600/month)., • Participate in customer calls, screen shares, or trainings when escalations require higher-level communication.Qualifications Here's What We're Looking For: • 2+ years in a customer-facing technical support role (B2B SaaS or eCommerce preferred)., • Experience using Zendesk (tickets, macros, views, Help Center)., • Ability to rotate into holiday or on-call support schedules as needed., • Familiarity with Jira, DataDog, browser developer tools, and analyzing logs or error messages., • Strong verbal and written communication skills; able to break down complex issues for technical and non-technical audiences., • Ability to self-prioritize in a high-volume support environment (600+ monthly solved tickets expected)., • Demonstrated initiative in bug tracking, internal documentation, or team training support., • Strong organizational and time-management skills; comfortable with ticket queues, call logs, and daily targets., • Background in hospitality or hotel technology (e.g., PMS, eSign/ePay systems) is a plus., • Experience with SOP creation is a plus. Additional Information What We Offer: • Competitive compensation, including Restricted Stock Units, • Employee Stock Purchase Plan (ESPP), • Flying Start - Our immersive Global Induction Program, • Work with brilliant people that will keep you on your toes, learn more about their journeys by checking out #InsideFlywire on social media, • Dynamic & Global Team (we have been collaborating virtually for years!), • Wellbeing Programs (Mental Health, Wellness) with Global FlyMates, • Be a meaningful part in our success - every FlyMate makes an impact, • Competitive time off including FlyBetter Days to volunteer in a cause you believe in and Digital Disconnect Days! We are excited to get to know you! Throughout our process you can expect to meet with different FlyMates including the Hiring Manager, Peers on the team, the VP of the department, and a skills assessment. Your Talent Acquisition Partner will walk you through the steps and be your “go-to” person for any questions. The US base salary range for this full-time position is $55,000-$60,000 plus restricted stock units and benefits. Our salary ranges are determined by role, position level, and location. The range displayed on this job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and several other factors, including job-related skills, experience, relevant education and training. Your Talent Acquisition Partner can share more about the specific salary range for your preferred location during the hiring process. Flywire is an equal opportunity employer. With over 30 nationalities across 12 different offices, and diversity and inclusion at the core of our people agenda, we believe our FlyMates are our greatest asset, and we’re excited to watch our unique culture evolve with each new hire. Flywire is an equal opportunity employer.

Job Description Join JB&B and shape the future of the built environment! Founded in 1915, Jaros, Baum & Bolles has been a pillar of engineering innovation in New York City for over a century. Specializing in mechanical, electrical, plumbing (MEP), JB&B has contributed to some of the most iconic buildings. In October 2025, JB&B joined forces with Trinity Consultants, a global consulting firm focused on the natural and built environments. JB&B now operates within Trinity’s Built Environment division, combining its deep expertise in high-performance building systems with Trinity’s strengths in acoustic design, facility operations, commissioning, and technology strategy. This strategic merger expands JB&B’s capabilities and offers employees: • Access to a broader portfolio of international projects and clients, • Enhanced career mobility across Trinity’s global network As an Associate, you’ll lead project teams, mentor junior staff, and collaborate with firm leadership to deliver high-quality engineering solutions and drive business development. Key Responsibilities • Lead conceptual design efforts, including system criteria, equipment room sizing, and building stack development, • Guide project teams through construction documentation and project completion, • Manage review of shop drawings, RFIs, contractor change orders, and conduct site visits and punch lists, • Establish and manage project schedules, ensuring efficient resource use and timely task completion, • Prepare proposals and additional services; coordinate reviews and approvals with Partners, • Coach and mentor staff, provide performance feedback, and support professional development goalsMinimum Qualifications, • Bachelor’s degree in electrical or mechanical Engineering, • 10–14 years of electrical engineering experience, • Proficient in design calculations and software tools such as Revit and AutoCAD, • Strong project management and leadership skills, • Deep understanding of trade-specific scopes, codes, and coordination with other disciplines, • Knowledge of documentation requirements for all project phases (SD, DD, CD, specifications)Why Work at JB&B?, • Legacy + Innovation: Our company blends a rich history with forward-thinking design, including smart building systems and deep carbon reduction strategies., • Collaborative Culture: With over 400 professionals, our company fosters mentorship, teamwork, and continuous learning., • Global Impact: Now part of Trinity, our company offers opportunities to work on transformative projects across commercial, healthcare, aviation, life sciences, and data center sectors., • Multiple office locations: New York, Boston and Philadelphia. What We Offer, • Hybrid workplace offering the flexibility to work both from home and the office, • Comprehensive benefits package including 401k employer match and stock options, • Paid time off (PTO), volunteer program and employee resource groups Jaros, Baum & Bolles is an equal opportunity employer. All qualified candidates will receive consideration for employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, marital status, military veteran status, unemployment status, or any other status protected by law. Powered by JazzHR VUFLZLsfCd

Job Description The Customer Service Associate provides a best-in-class experience for our customers by offering assistance, providing fast accurate cashiering duties and answering questions while maintaining a friendly and welcoming demeanor. Duties & Responsibilities • Provide the highest level of customer service to each customer, • Greet customers and assist them with product selection and product information, • Replenish, arrange, fold/straighten merchandise on the floor, • Operate the cash register while following cash handling procedures, • Assist with floor moves and inventory counts, • Previous customer service experience preferred, • Previous cash handling experience preferred, • Ability to speak clearly and effectively with customers, co-workers and managers, • Self-motivated outgoing person, • Strong multitasking skills, • Stays calm under pressure and can handle busy rush periods in store, • Ability to stand and walk for long periods of time, • Demonstrated commitment to teamwork and customer satisfaction Looking for up to 40 hours a week during the season. Game day availability is required with this position.

Job DescriptionCompany Description Abercrombie & Fitch Co. is a global, digitally led omnichannel specialty retailer of apparel and accessories catering to kids through millennials with assortments curated for their specific lifestyle needs. The company operates a family of brands, including Abercrombie & Fitch, YPB, abercrombie kids, Hollister and Gilly Hicks, each sharing a commitment to offer products of enduring quality and exceptional comfort that support global customers on their journey to being and becoming who they are. Abercrombie & Fitch Co. operates over 750 stores under these brands across North America, Europe, Asia and the Middle East, as well as the e-commerce sites abercrombie.com, abercrombiekids.com, and hollisterco.com. At Abercrombie & Fitch Co., we lead with purpose and always put our people first. Job Description The Key Lead is responsible for ensuring all customers receive quality in-store experience. They do this by acting as the Floor Supervisor, providing guidance and coaching to Brand Reps and Stock Associates ensuring store operations are running effectively. The Key Lead is part of the store leadership team, responsible for driving store performance on the floor through customer experience and team achievement of daily sales. What You’ll Do Open and Closing Routines Product Knowledge & Brand Awareness Business Understanding Proactive Thinking Attention to Detail Register/Point of Sales use Asset Protection Visual Displays System Skills Work Schedule Requirements -Schedule will vary weekly but should expect to work at least 12-16 hours per week. -Required availability on Saturdays and Sundays as well as certain holidays. -In addition, during peak timeframes, hours will increase to support the needs of the business. Qualifications What it Takes Education- High School Diploma/ G.E.D. equivalent preferred Retail Experience- At least 1 year of retail experience is preferred. Supervisor/ Managerial Experience- No supervisory/ management experience is required. Customer Focus Communication Interpersonal Interaction Fashion Trend Knowledge Outgoing Assertiveness Adaptability/Flexibility & Stress Tolerance Poise & Ambition Multi-Tasking Applied Learning Work Ethic Omni Channel Services Additional Information What You’ll Get As an Abercrombie & Fitch Co. (A&F Co.) associate, you’ll be eligible to participate in a variety of benefit programs designed to fit you and your lifestyle. A&F is committed to providing simple, competitive, and comprehensive benefits that align with our Company’s culture and values, but most importantly – with you! We also provide competitive incentives to reward the commitment our associates have for moving our global business forward: Quarterly Sales Incentive Bonus Merchandise Discount Flexible Schedule Opportunities for Career Advancement Opportunity to Become a Brand Affiliate Training and Development A Global Team of People Who'll Celebrate you for Being YOU The starting rate for this position is $18.85 per hour (i.e., the recruiting pay range for this position is $18.85 - $18.85 per hour). The starting rate and range may be modified in the future. FOLLOW US ON INSTAGRAM @LIFEATANF Abercrombie & Fitch Co. is an Equal Opportunity employer

Job Description We are seeking a detail-oriented and organized Warehouse Supervisor to join our team. This role oversees daily warehouse operations, including staff management, inventory control, and logistics, ensuring efficiency, accuracy, and safety in receiving, storing, and shipping goods, while also training teams and optimizing processes for productivity. The ideal candidate will have experience with inventory management systems, strong analytical skills, and a commitment to accuracy. Key Responsibilities: • Act as No 2. To the WH Manager, supervise, train, motivate, and provide feedback to the warehouse team of five., • Coordinate all inbound/outbound logistics, including loading, unloading, picking, packing, and shipping., • Maintain accurate stock levels, conduct cycle counts, resolve discrepancies, and manage warehouse layout., • Enforce company policies and safety regulations to ensure a secure work environment., • Identify and implement strategies to increase efficiency and reduce costs., • Coordinate with the client success team to ensure OTD of shipments to our customers., • Monitor inventory levels and coordinate with purchasing and warehouse teams to replenish stock as needed., • High school diploma or GED required, associate or bachelor’s degree preferred., • 2+ years of experience in inventory control and warehouse operations., • Forklift certification, • Experience with ERP systems (e.g., Visual, SAP, Oracle, NetSuite)., • Strong leadership, communication, and problem-solving skills., • Familiarity with lean manufacturing or just-in-time inventory principles.

Job Description Apiphani is a technology-enabled managed services company dedicated to redefining what it means to support mission-critical enterprise workloads. We're a small but rapidly growing company, which means there's lots of room for growth and learning opportunities abound! Apiphani is dedicated to creating a diverse and inclusive work environment for all as a fundamental component of our business. Diversity and inclusion are the bedrock of creativity and innovation. Without diversity of experience and thought, we would fail to progress as a company and as a team. Apiphani strives to foster an environment of belonging, where every employee feels respected, valued, and empowered. We embrace the unique experiences, perspective, and cultural background, which only you can bring to the table. We are looking for a highly organized and proactive Office Administrator / Executive Assistant (70% / 30%) based in Boston to ensure smooth daily office operations while providing partial executive support to the leadership team. This role is not a progression into a full-time Executive Assistant position. Instead, it is a combined role where the primary focus (approximately 70%) is on office administration and operations, with around 30% of responsibilities dedicated to Executive Assistant support for senior leaders. The ideal candidate is detail-oriented, reliable, an excellent communicator, and able to manage multiple priorities while serving as a key operational point of contact for the Boston office. Key Responsibilities Office Administration & Operations (70%) • Visit the office twice a week (or more frequently if required) to monitor office needs, including supplies (water, beverages, snacks), and place orders. • Manage procurement of office supplies, stationery, and operational materials., • Check the company mailbox, collect correspondence, scan documents, and distribute them to relevant stakeholders., • Act as the primary local point of contact in Boston for building management, landlords, and office-related vendors., • Manage office access and security processes, including issuing access cards, maintaining access lists, and coordinating access for new hires and visitors., • Own all communication with the new building, including access, safety, and operational matters., • Support office relocation activities, including vendor coordination, meetings related to furniture, AV systems, office security, budget coordination, and redistribution of furniture from the previous office., • Oversee fire drill coordination and compliance with building regulations., • Book meeting rooms and coordinate catering for internal meetings. • Manage calendars for 6+ senior leaders across multiple time zones., • Coordinate travel logistics including flights, hotels, and ground transportation., • Prepare and refine presentations and manage documents in SharePoint., • Act as a liaison between leadership and the Associate Chief of Staff., • Assist in organizing conferences and exhibitions., • Coordinate printed materials and branded giveaways., • Track deadlines and delivery logistics for events. Requirements • Based in Boston with ability to visit the office at least twice a week. • Previous experience as an Office Administrator, Office Manager, or Executive Assistant., • Strong organizational and multitasking skills., • Experience managing executive calendars and travel., • Proficiency in Microsoft Office Suite and SharePoint., • Experience working with vendors and organizing events., • Excellent communication skills and high level of discretion. Base Salary€65.000—€75.000 EURCompany Benefits • Medical/dental/vision - 100% paid for employees, 50% paid for dependents, • Life and disability - 100% paid for employees, • 401K - 3% contribution, no employee contribution necessary, • Education and tuition reimbursement - up to $50K annually, • Employee Stock Options Plan, • Accident, critical illness, hospital indemnity benefits offered through our providers, • Employee Assistance Program, • Legal assistance, • Paid Time Off - up to 6 weeks per year, • Sick Leave - up to 2 weeks per year, • Parental Leave - up to 12 weeks

Job DescriptionDescription: Citrus & Salt in the Seaport is looking to a hire a full time assistant general manager to join their team. Develops, implements and maintains quality standards for restaurant and facility, including supervision and direction of service staff. Ensures excellent customer service standards are maintained. Leads in creating Memorable Guest Moments. Essential Duties: ? Organizes and conducts pre-shift meetings to review specials, menu changes, house counts, etc. ? Ensures that the restaurant and restaurant facilities are kept clean, well-stocked and organized. ? Checks the maintenance of all equipment in the restaurant and schedules needed maintenance and repair. ? Circulates throughout the restaurant facilities and kitchen areas to visually monitor and take action to ensure food quality and service standards are met. ? Greets guests at tables to ensure complete guest satisfaction and attention to guest needs. ? Ensures established cash handling procedures are utilized to accurately charge customers. ? Creates sales and log reports. Monitors restaurant budget and takes action to minimize expenses. Reports on financial performance, inventory, and personnel. ? Tracks stock levels of food, china, glassware, silverware, and other supplies and equipment, forecast needs, and oversees ordering as necessary. ? Conducts regular inventory counts and implements procedures to monitor assets. ? Oversees daily restaurant activities to include serving tables, bussing tables, seating guests, room service and general clerical/cashier duties. ? Responsible for working with GM in interviewing, hiring, training, planning, assigning, and directing work, evaluating performance, rewarding, and disciplining associates; addressing complaints and resolving problems. ? Manages department members that may include, but is not limited to: Hosts, Servers, Bartenders, and Bussers. ? Assures that effective orientation and training are given to each new associate. ? Develops ongoing training programs and tests for comprehension. ? Adheres to and enforces employee compliance with health, safety, and sanitation standards. ? Regular and reliable attendance. ? Incorporates safe work practices in job performance. Requirements:Preferred Requirements: administration, or a related field? Previous Managerial Experience? Experience in restaurant point-of-sale (POS) systems and on-line Reservation Systems, Inventory Controls, Scheduling/Labor Management, Financial Forecasting? Experience in Purchasing, inventory management, sanitation, security, company policies and procedures, personnel management, record keeping, and preparation of reports.

Job DescriptionDescription: Job Overview: We are seeking a hard working and reliable Counter Sales Associate to join our team as part of the Buttermilk & Bourbon Group. The ideal candidate will be customer-oriented, able to work as a team, and thrive in a fast-paced environment. Duties: • Greet customers and place food orders & deliver to tables, • Process sales transactions accurately using Toast Point of Sale (POS) system, • Maintain a clean and organized work environment, • Provide menu knowledge and recommendations to customers, • Upsell items to maximize sales, • Handle guest inquiries and resolve issues promptly, • Re-stock shelves and monitor inventory levels Experience: • Previous experience in food sales or customer service is required, • Strong communication skills with attention to detail, • Experience using Toast POS is preferred but not required, • Ability to upsell and cross-sell items effectively, • Experience cash handling is required This position offers opportunities for growth and development within a fast growing company. If you are passionate about delivering exceptional customer service and have the skills required, we encourage you to apply for this exciting opportunity and look forward to working with you! Job Type: Part-time Pay: $16.00 - $19.00 per hour + tips Benefits: • Employee discount, • Day shift, • Evening shift Experience:

Job Description Job Title: Manufacturing Associate – Cell Therapy Production Job Description We’re seeking a Manufacturing Associate to join our growing team focused on the production of T cell and TCR-engineered therapies. This role is ideal for someone with strong GMP experience, a proactive mindset, and a commitment to quality and safety in a cleanroom environment. Responsibilities • Operate production equipment and perform processing steps in compliance with GMP standards., • Accurately complete production documentation and batch records., • Maintain cleanliness and organization of the production area., • Stock and manage supplies to ensure uninterrupted operations., • Troubleshoot equipment and process issues to maintain operational efficiency., • Support or lead Commissioning and Validation activities., • Assist in the creation and revision of manufacturing documentation., • Identify and implement continuous improvement opportunities., • Ensure compliance with cGMP, safety protocols, and regulatory requirements., • Associate’s or Bachelor’s degree in a scientific or related field., • 5+ years of experience in cleanroom or GMP manufacturing environments., • Hands-on knowledge of T cell therapy and TCR-engineered cell therapies, with a minimum of 2-3 years of experience., • Experience with both upstream and downstream manufacturing., • Strong understanding of GMP, batch record review, and biologics production., • Experience with controlled document creation and review., • Excellent documentation and communication skills., • Proficiency in Microsoft Word, Excel, Outlook, and PowerPoint., • Must be able to read, write and speak English fluently., • Ability to lift and transport packages weighing up to 50 pounds., • Extensive walking throughout the facility will be required. This is a Contract position based out of Waltham, MA. Pay and Benefits The pay range for this position is $40.00 - $46.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Waltham,MA. Application Deadline This position is anticipated to close on Feb 6, 2026. 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.

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/liliProvide feedback to supervisor regarding inventory levels and da

The Stock Associate maintains effectiveness of merchandise flow, filling and presentation standards throughout the store and stock. Abercrombie & Fitch - Stock Associate, Faneuil Hall. Stock Associates typically work three to four shifts per week on average, each shift being about four to five hours

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/liliProvide feedback to supervisor regarding inventory levels and da

Maintain (stock, rotate stock, and clean) the general storeroom, walk-in coolers, and main kitchen freezer in accordance with general stocking practices and serve safe requirements, to ensure wholesome, quality food and beverage. Maintain (stock, rotate stock, and clean) the general storeroom, walk-

Exemplify the highest level of customer service standards to internal and external customers/ppScan shipment as delivered/ppTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/ppProvide feedback to supervisor regarding inventory levels and damages/

You can't buy product if it's not on the floor, right?! As a part-time stock brand ambassador, you're an expert at keeping product moving from the stockroom to the salesfloor through shipment processing, replenishment, markdowns, and merchandising. The stockroom is your home base and you #ownit! You

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/li/ululliProvide feedback to supervisor regarding inventory levels a

Maintain (stock, rotate stock, and clean) the general storeroom, walk-in coolers, and main kitchen freezer in accordance with general stocking practices and serve safe requirements, to ensure wholesome, quality food and beverage. Maintain (stock, rotate stock, and clean) the general storeroom, walk-

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/liliProvide feedback to supervisor regarding inventory levels and da

You can't buy product if it's not on the floor, right?! As a part-time stock brand Ambassador, you're an expert at keeping product moving from the Stockroom to the Salesfloor through shipment processing, replenishment, markdowns and merchandising. The Stockroom is your home base and you own it! You'

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/li/ululliProvide feedback to supervisor regarding inventory levels a

This Stock Associate Job Is For You, If You Enjoy:. Your Team Is Counting On You As A Stock Associate To:. Protects all company assets in the stock area including non-stock merchandise.

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/liliProvide feedback to supervisor regarding inventory levels and da

You can't buy product if it's not on the floor, right?! As a part-time stock brand Ambassador, you're an expert at keeping product moving from the Stockroom to the Salesfloor through shipment processing, replenishment, markdowns and merchandising. The Stockroom is your home base and you own it! You'

Exemplify the highest level of customer service standards to internal and external customers/ppScan shipment as delivered/ppTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/ppProvide feedback to supervisor regarding inventory levels and damages/

Actively participate in all merchandising activities including, but not limited to: daily stock maintenance and order, stock receiving and processing, product transfers, maintaining sales floor standards, and flips. Must be able to pack, unpack and move stock when supporting in receiving / stocking

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/liliProvide feedback to supervisor regarding inventory levels and da

Stock Associate Job Duties: Receives and inspects product.

Protects all company assets in the stock area including non-stock merchandise. This Stock Associate Job Is For You, If You Enjoy:. Your Team is counting on you as a Stock Associate to:.

Stock shelves, racks, cases, bins, and tables with new or transferred merchandise. Ability to be mobile on the sales floor and stock rooms for extended period of time in a fast paced environment.

Ensure accurate and effi Stock Associate, Associate, Operations, Customer Experience. Process and replenish merchandise as needed, receive and monitor floor stock, and handle product movement in and out of the store.

This is an exciting opportunity to join Balenciaga's Boston Copley Place team as a Stock Associate who will drive the business and contribute to the brand philosophy. We are currently seeking a Stock Associate who will report to the Store Director. The Stock Associate is also responsible for process

Exemplify the highest level of customer service standards to internal and external customers/liliScan shipment as delivered/liliTicket and stock merchandise in the stock room or prepare for immediate distribution to the sales floor/liliProvide feedback to supervisor regarding inventory levels and da

Stock Associate Job Duties: Receives and inspects product.