Jobs in Mansfield: Warehouse Operator, Medical Device Assemblers, and More!

Warehouse Operator at Medline Industries, Inc.

We are seeking a dynamic, hard-working people.  A desire to work for a fast-paced, large corporate organization is a plus.  In addition you must have a “roll-up your sleeves” attitude.

The challenging responsibilities of the position include:

• Reads production schedule, customer order, work order, shipping order, or requisition to determine items to be moved, gathered, or distributed.
• Conveys materials and items from receiving or production areas to storage or to other designated areas.
• Sorts and places materials or items on racks, shelves, or in bins according to predetermined sequence such as size, type, style, color, or product code.
• Fills requisitions, work orders, or requests for materials, tools, or other stock items and distributes items to production workers or assembly line.
• Assembles customer orders from stock and places orders on pallets or shelves, or conveys orders to packing station or shipping department.
• Marks materials with identifying information.
• Opens bales, crates, and other containers.
• Housekeeping duties including all forms of warehouse cleanup not limited to waste, wood, general refuse disposal, wiping, wet and dry cleaning, sweeping and/or mopping inside and outside.
• Records amounts of materials or items received or distributed.
• Weighs or counts items for distribution within plant to ensure conformance to company standards.
• Arranges stock parts in specified sequence for assembly by other workers.
• Compiles worksheets or tickets from customer specifications.
• Operates hand truck, cart, dollies, forklift, “man-up” order-picker, and walkie to transport stored items from warehouse to plant or to pick up items from several locations for shipment.

In return, Medline offers a business casual, entrepreneurial work environment with strong growth potential; a competitive compensation package; along with a complete benefits package including medical/dental/vision/life insurance; education assistance; 401(k) with company match and much more!

The required skills for this position are:

• High school diploma or general education degree (GED).
• One to three months related experience and/or training.
• Equivalent combination of education and experience.
• Ability to speak, read, and write English with proficiency. 
• Ability to read and comprehend simple instructions, short correspondence, and memos.
• Basic keypunch skills needed.

Medline Industries, Inc. is an Equal Opportunity, Affirmative Action and Drug Free Employer.

Two Medical Device Assemblers Needed at Randstad

Two medical device assemblers for a 4+ month contract that has the opportunity to turn into a permanent position. The position is located in Mansfield. You must have at least two years of experience with small assembly and or detailed soldering. If you have clean room and or medical device experience it is considered a plus.

Requirements:

• At least 2 years of experience of small assembly and or detailed soldering
• preferred experience in clean room environment
• preferred medical device assembly experience
• Reliable transportation

Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.

Host/Hostess at Bertucci’s

Want to join the Bertucci's family? It’s a great place to work! We're always looking for outgoing people who are passionate about what they do. If that sounds like you, we'd love to meet you!

Work in a team-oriented, high-volume, fast-paced, guest-centric environment to treat our guests “The way they want to be treated” by:

• Demonstrating genuine hospitality and setting the stage for an exceptional Dining Experience by making every single guest feel welcome at the door 
• Engaging in friendly conversation as you seat guests in a timely fashion
• Introducing guests to their server
• Managing restaurant waiting list during high volume to accurately set guest expectations
• Always sincerely thanking guests as they leave and inviting them to return

Job Benefits:

• Group Accident Insurance
• Group Critical Illness Insurance
• Medical
• Vision
• Dental
• Term Life
• Short Term Disability
• College Savings-529

Assistant Store Manager at Rite Aid 

The associate may be responsible for all or some of the functions below, in addition to other duties as assigned:

• Assist the Store Manager with the operation of the retail store including lead associates through the execution of company business plans/objectives to drive sales, be profitable and provide a superior customer and associate experience.
• Enforce all policies and procedures to ensure excellent customer service is provided and to maximize the P&L performance of the store.
• Assist with the general maintenance and appearance of the store by ensuring a safe and pleasing environment for both customers and associates; request store maintenance when required.
• Ensure the store opens and closes at the appropriate time and the proper procedures are followed for cash transactions and bank deposits.
• Interact with vendors to order ad, seasonal, and basic merchandise and ice cream (where applicable) for the store.
• Merchandise the seasonal aisle and non-seasonal, basic, and seasonal end-caps; ensure all merchandise is set up according to plan-o-grams received from the corporate office.
• Execute weekly sales ads and price changes; process recalled, damaged, outdated, and transferred merchandise.
• Receive merchandise deliveries from vendors and Rite Aid distribution centers; verify vendor invoice information is accurate and enter vendor invoices into the accounts payable system.
• Prepare the retail store for physical inventory by ensuring merchandise on the sales floor and in the stock room is in order and easy to access.
• Analyze operating reports and make recommendations for improvement.
• Utilize Staffworks® /Workforce Management software to complete the associate work schedule.
• Remain knowledgeable of the One-Hour Photo department and film processing, if applicable.
• Assist the Pharmacy department when there is a high volume of customers.
• Provide leadership and development for associates by communicating career opportunities, providing regular performance feedback, and demonstrating RAPTAR (Recognition, Appreciation, Praise, Treat Associates Respectfully) behaviors.
• Manage the adherence to all regulatory and compliance legislation and policies.
• Ensure that all outdated product and product with less than 30 days until expiration is removed from the sales floor to be processed through the established returns process.

 Supervisory Responsibilities:

This position may involve managing tasks and supervising other store associates in accordance with Rite Aid policies and applicable laws. Responsibilities may include interviewing, hiring, training, directing, rewarding, and disciplining associates; appraising associate performance; and resolving complaints.

Education:

At least two (2) years of experience in retail, food service, restaurant or customer service industry, preferably at a supervisor level, and/or a two (2) year college degree.

Associate Director Regulatory Affairs at Covidien

The Associate Director Regulatory Affairs will lead a team with responsibilities of the support of Product Development, Marketing, Domestic and European product registrations and support of Regulatory activities including but not limited to: 

• Direct team in the management of product development/change projects to set and integrate regulatory submissions strategy into development/change activities
• Direct Regulatory Affairs Managers and Specialists in the management of their teams for the preparation of submissions (i.e. 510k, CE marking applications, technical documentation, product registrations, etc.) to obtain various worldwide approvals to commercially distributed medical products. Produces subsequent submissions (renewals, change notifications, etc.) to facilitate the maintenance of these approvals
• Determine applicable registration requirements for medical devices in all countries in which products are to be registered
• Interpret and/or evaluate proposed registration requirements for medical devices and advise on impact of such regulations on the company
• Coordinate complex logistical details including resource and project timeline planning, liaison with functional group representatives and identification/coordination of source documentation
• Manage and/or oversee communication and submission processes of global registrations including general correspondence, reports and amendments
• Coordinates submission issues interdepartmentally to ensure compliance and quick and complete resolution
• Assist Covidien domestic and international manufacturing facilities with foreign government and regulatory body inspections
• Coordinate international registration and appropriate export application forms for Covidien Vascular Therapies products intended to be exported to foreign countries
• Review device labeling and advertising materials for compliance with regulations
• Maintain proficiency on global regulatory requirements and develop and maintain rapport with regulatory reviewers and project team members
• Plans and implements regulatory policies, procedures, practices, and strategy as required

Essential Functions:

• Effective management and leadership skills, as well as effective oral/written communication skills
• Ability to budget for future expenditures and manage departmental budget
• Ability to work effectively in a team environment
• Ability to prepare and execute effective presentations
• Effective negotiation and team building skills and ability to manage critical decision-making through the use of consensus
• Ability to interface with all levels of management and regulatory body representatives.
• Ability to move from department to department to attend meetings and interact with others.
• Organization and preparation of final regulatory filings (e.g. product submissions and site/establishment registrations)
• Review change control documents and ascertain regulatory impact
• Collaborate with internal Covidien departments to obtain and understand registration documents
• Act as liaison with International Covidien Regulatory Personnel to address questions and issues that arise as part of the registration and/or testing process
• Understand and recommend strategies based on current local registration requirements and applicable industry standards
• Understand competitive technologies
• Understand local country quality requirements (e.g. ISO, QSR)
• Drive process and system changes

• Bachelors Degree in scientific discipline                    
• 7-10 years Regulatory/Quality Experience

Preferred Skills/Qualifications:           

• Skills/Competencies:
•  Strong organizational skills
• Ability to problem solve
•  Ability to work well with others
•  Team Oriented
•  Excellent written and oral communication skills
•  Fluent in local language required

Travel Time required, up to 10%