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<h3>Job Description</h3>
Job Description
Job Title: Material and Production Planner
Department: Supply Chain
Reports to: Sr. Director of Supply Chain &amp; Logistics
FLSA Status: Exempt

Job Summary and Objectives:
The Material and Production Planner is responsible for ensuring the timely and efficient flow of materials and production schedules to meet customer demand and organizational goals. This role involves planning, coordinating, and monitoring material requirements, production activities and inventory levels to optimize supply chain performance and minimize cost.
Essential Duties and Responsibilities:
Develop and maintain material requirement plans for sales forecasts, production schedules and inventory targets. Manage safety stock levels/re-order points and adjust plans to prevent material shortages or excess inventory. Use formal systems, such as DelmiaWorks ERP, to plan the production process from start to finish. 
- Partner with NextPhase customer service, manufacturing, and engineering to provide rough-cut capacity planning for both current demand and future forecast.
- Have full understanding of customer contracts.
- Work closely with NextPhase supply chain to ensure material availability prior to scheduling work orders in manufacturing.
- Create and update production schedules to align with customer orders and capacity constraints. Identify and resolve scheduling conflicts or bottlenecks to maintain on-time delivery.
- Partner with logistics to ensure that products ship on time and arrive on time at customer and sterilization sites.
- Track effectiveness and recommend improvements and solutions.
Optimize execution of internal work orders to achieve schedule adherence, and customer on-time delivery goals. Identify and implement continuous improvement ideas to reinforce reliability of delivery using LEAN and Six Sigma techniques.
- Work with suppliers and NextPhase buyers to identify and optimize reliability of supply and information to support manufacturing and business objectives.
- Contribute to defining and implementing cost reduction opportunities with suppliers and customers.
- Contribute to supplier corrective actions and make supplier recommendations in conjunction with NextPhase buyers.
Required Qualifications and Work Experience:
<ul>
<li>Bachelor’s Degree in appropriate field of study or equivalent work experience required</li>
</ul>
<ul>
<li>Minimum of 5 years’ relevant planning experience in manufacturing industry, with 2 additional years in a medical field, or other highly regulated industry</li>
<li>Demonstrated ability to develop and maintain strong partnerships at all levels of the organization, to further the goals and advancement of the department's objectives</li>
<li>Proficiency with planning and scheduling systems, ERP/MRP systems, and inventory management techniques.</li>
<li>Demonstrated ability using LEAN tools and concepts</li>
<li>Proficiency with Microsoft Office (Word, Excel, PowerPoint, Teams, SharePoint, AI Platforms)</li>
<li>Demonstrated ability to work in a cross-functional team environment.</li>
</ul>
<ul>
<li>Effective collaborative leadership style and experience</li>
<li>Excellent communication skills (written and verbal), problem solving abilities, and creative solution generation</li>
</ul>

Preferred Qualifications and Work Experience:
<ul>
<li>Master’s Degree in related field</li>
<li>10+ years’ experience planning in a MedTech manufacturing environment </li>
<li>5+ years’ experience in medical device contract manufacturing</li>
<li>LEAN training or certification</li>
<li>Six Sigma Black Belt certification</li>
<li>Experience with DelmiaWorks (formerly IQMS) ERP</li>
</ul>

Physical Demands:
<ul>
<li>Ability to sit and work at a computer for extended periods of time (up to 8 hours per day)</li>
<li>Occasional lifting up to 30 lbs.</li>
<li>Ability to enter and work in a cleanroom environment when required</li>
</ul>

Work Environments:
<ul>
<li>Physical Setting: Busy, professional office and manufacturing environment </li>
<li>Culture: A diverse and inclusive culture that respects and values individual contributions </li>
<li>Dress Code: Business casual attire to promote a professional yet comfortable workplace</li>
<li>Core Business Hours: 8:00am to 5:00pm</li>
</ul>

Additional Information:
<ul>
<li>Occasional travel to customer or supplier sites may be required</li>
</ul>

On-Site/Remote Attendance:
<ul>
<li>This position requires 100% on-site attendance in Rochester, New Hampshire</li>
</ul>

Job Description is a Guideline Only
<ul>
<li>This job description is a summary of the main functions and responsibilities of this position as it currently exists. It is not intended to be a complete and exhaustive list or description and may evolve and change over time in accordance with business and market demands. Duties, responsibilities and activities may change at any time with or without notice.</li>
<li>This job description is also not a contract, and ARTEREX may from time-to-time in its discretion revise, amend, and update this job description to better reflect the actual functions and responsibilities the employee performs.</li>
</ul>

Equal Employment Opportunity Statement:
<ul>
<li>ARTEREX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected veteran status.</li>
</ul>

MATERIAL AND PRODUCTION PLANNER

<h3>Job Description</h3>
Job Description
About Divert
Divert is a circular economy company on a mission to prevent food from being wasted through nationwide infrastructure and innovative technologies. Founded in 2007, the company provides an end-to-end solution that leverages data to prevent waste, facilitates edible food recovery to provide to people in need, and transforms unsold food products into renewable energy to power communities. Through this integrated approach to reducing wasted food–Prevent, Provide, Power™–Divert works with customers across the U.S. to reduce wasted food and positively impact people and the environment.
What You'll Do:
The Process Engineer is the key engineering point of contact for Divert’s Operations teams. The role is critical in ensuring transparent, two-way communication between Operations and central Engineering as well as consistent implementation of best practices across all Divert’s facilities. The Process Engineer owns communication and resolution tracking for process performance issues.
Responsibilities
Process Oversight &amp; Issue Identification:
<ul>
<li>Monitor and review the technical performance of key systems, including the anaerobic digesters, RNG production, air scrubbers, centrifuges, and automated equipment.</li>
<li>Detect and report any deviations or malfunctions to the appropriate subject matter experts and Plant Director.</li>
</ul>
Prioritization &amp; Action Planning:
<ul>
<li>Assess the criticality of identified issues based on their potential impact on safety, production, or regulatory compliance.</li>
<li>Develop and maintain a prioritized action item list, ensuring prompt attention to the most urgent matters and tracking and communicating frequently all issues through resolution.</li>
</ul>
Technical Coordination:
<ul>
<li>Serve as the on-site point of contact between Plant Operations and centralized or external SMEs in:</li>
<li>Controls/Automation – reviewing PLC/SCADA data and ensuring system reliability.</li>
<li>Biological Processes – coordinating with microbiologists to maintain optimal digester conditions.</li>
<li>Mechanical/Chemical Systems – working with mechanics and chemical engineers on equipment performance, component integrity, and chemical usage.</li>
<li>Clearly communicate on-site strategies and constraints to specialized teams, enabling rapid and accurate troubleshooting.</li>
</ul>
Incident Response:
<ul>
<li>Lead technical investigations of process failures to determine root causes and ensure corrective actions are implemented.</li>
<li>Issue a written summary of these technical investigations so future failures and incidents can be understood and reported to engineering SME and Plant Operations for other preventative actions.</li>
</ul>
Communication &amp; Collaboration:
<ul>
<li>Provide concise, regular updates to management and cross-functional teams regarding process performance, technical issues, and resolution timelines.</li>
<li>Ensure clear, efficient coordination between on-site personnel, external technical vendors, and subject matter experts.</li>
</ul>
What we're looking for:
<ul>
<li>Bachelor degree in Chemical or Mechanical Engineering.</li>
<li>5+ years experience working in a processing facility.</li>
<li>Exceptionally strong communication skills, written, verbal and relationship building.</li>
<li>Ability to travel up to 10% to facilities across the US</li>
</ul>
What's In It For You?
<ul>
<li>Compensation range: $120-135K annually</li>
<li>Health, Vision and Dental Benefits (effective the first of the month following your date of hire!)</li>
<li>Life Insurance</li>
<li>401K with Safe Harbor company match</li>
<li>Paid Time Off</li>
<li>Opportunities for Advancement with a Rapidly Growing, Mission-Driven Organization</li>
</ul>
Divert Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Divert does not accept unsolicited resumes or candidate referrals from third-party recruiters or staffing agencies. Any resumes submitted in the absence of a signed agreement with our HR team will be considered property of Divert, Inc., and no fees will be paid in the event a candidate is hired. We kindly ask that external recruiters do not contact our hiring managers or employees directly.

Process Engineer (Plant Operations)

<h3>Job Description</h3>
Job Description Job Title: Tech Ops and Quality - Quality Control Analyst II Location: Norton, MA 02766 Duration: 11+ Months Description: The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness. This is an onsite role in Norton, MA, with occasional responsibilities at other Client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training. Key Responsibilities:
<ul>
<li> Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.</li>
<li> Support weekend lab operations and maintain training records.</li>
<li> Assist in lab equipment and inventory maintenance, including reagent and sample prep.</li>
<li> Review data timely and qualify as a data reviewer.</li>
<li> Perform operational assignments (raw material processes, environmental monitoring, in-process testing).</li>
<li> Contribute to updating controlled documents (SOPs, work instructions, test methods).</li>
<li> Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH).</li>
<li> Participate in continuous improvement initiatives and cross-functional collaboration.</li>
<li> Support regulatory submissions, inspection readiness, and audits</li>
</ul>
 Qualifications:
<ul>
<li> B.S. in chemistry, biology, biochemistry, or related field.</li>
<li> 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.</li>
<li> Experience in method transfer/implementation; understanding of method lifecycle management preferred.</li>
<li> Strong technical writing, data analysis, problem-solving, and organizational skills.</li>
<li> Excellent communication and teamwork.</li>
<li> Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred</li>
</ul>
 #TB_PH #ZR #ZR Company DescriptionFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website <a href="http://www.talentburst.com" target="_blank">www.talentburst.com</a> or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX &amp; downtown San Francisco, CA 
<h3>Company Description</h3>
Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website <a href="http://www.talentburst.com" target="_blank">www.talentburst.com</a> or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX &amp; downtown San Francisco, CA

Quality Control Analyst II

<h3>Job Description</h3>
Job Description
If you’re looking for a Manufacturing Production Associate job, then look no further! Adecco is looking for candidates who thrive in a fast-moving environment for this Manufacturing Associate job for a client in Arlington, VT, and we are hiring immediately! These manufacturing production opportunities will allow you to enhance your career while gaining valuable warehouseexperience. 
 Primary responsibilities include: 
<ul>
<li>
Operate different machinery to assemble and manufacture products 
</li>
</ul>
<ul>
<li>
Use small hand tools 
</li>
</ul>
<ul>
<li>
Clean and inspect parts 
</li>
</ul>
<ul>
<li>
Disassemble returned units 
</li>
</ul>
<ul>
<li>
Keep the work area clean 
</li>
</ul>
 What’s in it for you? 
<ul>
<li>
Competitive benefits with options such as medical, dental, vision, and 401(k) 
</li>
</ul>
<ul>
<li>
Weekly pay of $18.00 - $20.00/hr. (depending on shift) 
</li>
</ul>
Available Shifts: 
Please not some overtime may be required
<ul>
<li>
1st Shift: Monday - Friday - 7AM-3PM 
</li>
</ul>
<ul>
<li>
2nd Shift: Monday – Friday - 3PM-11PM 
</li>
</ul>
<ul>
<li>
3rd Shift: Monday – Friday - 11PM-7AM 
</li>
</ul>
For instant consideration on this Manufacturing Production Associate job, click on Apply Now!
 Pay Details: $18.00 to $20.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://uat.adecco.com/en-us/candidate-privacy" target="_blank">https://uat.adecco.com/en-us/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Manufacturing Production Associate

<h3>Job Description</h3>
Job Description
Position: Mechanical Engineer
Location: Nashua, NH
Amphenol High Speed Products Group is the market leader for high speed, high bandwidth electrical connectors for the Telecom/Datacom market (Mobile Networks, Storage, Servers, Routers, Switches, etc.). Our products help to enable the electronics revolution and remain a key enabler for all the major Tier 1 OEMs globally. Our global headquarters are located in Nashua, NH and we have design, sales and manufacturing locations globally. We are currently seeking a Mechanical Engineer to join our High Speed Engineering team. The position will be located in Nashua, NH.
RESPONSIBILITIES:
As a Mechanical Engineer on the HSIO Products team you willsupport to the design, development and selection of basic hardware components utilizing fundamental mechanical engineering principles, theories and techniques. Assigned duties may include:
<ul>
<li>Design and development of specific elements of High-Speed IO Interconnect and Cable devices or components to meet specified design requirements. May receive direction from senior engineering staff and may be responsible to provide direction to drafting.</li>
<li>Perform Mechanical Analyses- Obtain working knowledge of company standard analysis tools. Perform basic static, dynamic and heat transfer analyses of mechanical structures, when required. Compile data for investigation by senior mechanical engineering personnel. Participate in design reviews.</li>
<li>Support Verification/Validation of Design- Support the fabrication and environmental testing of High-Speed IO Interconnect devices. Assist in the design and fabrication of prototype hardware. Support the environmental testing of hardware including vibration, shock, thermal, fatigue and others as required. Document results for review by senior engineering personnel.</li>
<li>Prepare Documentation- Generate and review the technical content of drawings, engineering specifications, reports and other documentation associated with the mechanical design. Generate and present design review packages for internal and external audiences.</li>
<li>Support Continuous Improvement- Conduct failure analysis of product returned from field and qualification failures. Lead customization efforts on assigned product lines when required.</li>
<li>Lead sustainment efforts on assigned product lines- Provide Mechanical Engineering support to products in production. Manage material issues, perform root cause assessments of discovered issues. perform analysis as required to verify validity of proposed solutions.</li>
</ul>
QUALIFICATIONS:
<ul>
<li>BS Degree in Mechanical Engineering (MS preferred)</li>
<li>3-5 years of electromechanical product design/support experience</li>
<li>Strong Mechanical Aptitude</li>
<li>Familiarity with Structural and Thermal FEA software and capability.</li>
<li>Grasp of basic electrical theory.</li>
<li>Ability to support design and development of hardware to ensure requirements compliance</li>
<li>Ability to read mechanical drawings and perform tolerance assessments. Experience with ASME Y-14.5 is a definite plus.</li>
<li>Ability to perform basic mechanical analysis to ensure good design.</li>
<li>Proficiency with Solidworks 2018 or higher</li>
<li>Ability to conduct experimentation and basic testing. Familiarity with basic measurement tools and multimeters.</li>
<li>Good communication skills and organizational skills</li>
</ul>

Mechanical Engineer - HSIO

<h3>Job Description</h3>
Job Description
Position: Mechanical Engineer – Thermal 
Location: Nashua, NH 
Amphenol High Speed Products Group is the market leader for high speed, high bandwidth electrical connectors for the Telecom/Datacom market (Mobile Networks, Storage, Servers, Routers, Switches, etc.). Our products help to enable the electronics revolution and remain a key enabler for all the major Tier 1 OEMs globally. Our global headquarters is located in Nashua, NH and we have design, sales and manufacturing locations globally. We are currently seeking a Mechanical Engineer-Thermal to join our team in Nashua. 
RESPONSIBILITIES: 
<ul>
<li>Perform thermal simulations and analyses (steady-state and transient) using tools such as ANSYS Icepak, FloTHERM.</li>
<li>Design and optimize thermal solutions including heat sinks, fans, liquid cooling systems, and interface materials (PCM) for high speed I/O active cables and optical transceivers and fiber optic cables.</li>
<li>Conduct thermal characterization and validation tests, including temperature measurement, and correlation with simulation results.</li>
<li>Collaborate with mechanical, electrical, and systems engineers to integrate thermal solutions into overall product design.</li>
<li>Define thermal requirements and design constraints for new products and ensure compliance with reliability and performance specifications.</li>
<li>Develop and document thermal models, test reports, and design guidelines for future designs.</li>
<li>Participate in design reviews, providing recommendations for improved thermal performance and manufacturability.</li>
<li>Support failure analysis and root cause investigations of thermal-related field or qualification issues</li>
</ul>
QUALIFICATIONS: 
<ul>
<li>M.S. in Mechanical Engineering, or a related field, and 5 years applicable experience preferred </li>
<li>Solid understanding of mechanical and thermal principles, and material properties </li>
<li>Proficiency with thermal simulation tools like FLOTHERM, ANSYS Icepack.</li>
<li>Knowledge of electronics packaging and reliability requirements (JEDEC, IPC, standards) preferred</li>
<li>Experience in Electronics / Data Center / Telecom: Familiarity with high-power ICs, PCBs, heat spreaders, and airflow management is an added advantage.</li>
</ul>
Amphenol Corporation is proud of our reputation as an excellent employer. Our main focus is to provide the highest level of support and responsiveness to both our employees and our customers, the world's largest technology companies. Amphenol Corporation offers the opportunity for career growth within a global organization. We believe that Amphenol Corporation is unique in that every employee, regardless of his or her position, has the ability to positively impact the business.
Amphenol is an “Equal Opportunity Employer” - Minority/Female/Disabled/Veteran/Sexual Orientation/ Gender Identity or National Origin.
For additional company information please visit our website at <a href="https://www.amphenol-cs.com/" target="_blank">https://www.amphenol-cs.com/</a>

Mechanical Engineer- Thermal

<h3>Job Description</h3>
Job Description
InnoTECH Staffing has an immediate opening for a Sr. Quality Engineer to work in the Quality Department in a dynamic Medical Device Research and Development environment located in Manchester, NH.
This requires being onsite 5 days a week and must be a US Citizen or Greencard holder.
The position reports to the Director of Quality. We are seeking a Sr. Quality Engineer to provide Quality guidance in a dynamic, fast-paced medical device research, design assurance, manufacturing, and distribution environment. How you will make an impact as a Senior Quality Engineer: 
<ul>
<li>Work cooperatively with cross functional design team members and project management to determine the best approach for on-going compliance with applicable SOPs and regulations, such as 21 CFR 820 and ISO 13485.</li>
<li>Use critical thinking to determine the best approach.</li>
<li>Use experience within Design Assurance or production and processing of medical devices to provide guidance and assistance in the development of new products.</li>
<li>Participate and lead in Risk Management activities in accordance with ISO 14971:2019.</li>
<li>The development, implementation, and approval of Hazard Analyses, FMEAs, and other Risk Analysis documentation.</li>
<li>Use experience with engineering and technology to identify and ensure compliance with applicable standards and regulations.</li>
<li>Lead investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem-solving skills.</li>
<li>Coordinate the efforts of individuals and teams performing investigations.</li>
<li>Use experience within manufacturing and monitoring of medical devices, to provide guidance in Root Cause Analysis and CAPA.</li>
<li>Ensure the accurate documentation and recording of information to be used in communication with partners and regulatory bodies.</li>
<li>Prepare detailed work plans such as Master Validation Plans.</li>
<li>Lead system and process improvements using six sigma tools.</li>
<li>Provide reliability and statistical analysis.</li>
<li>Conduct test method validations for formal testing.</li>
<li>Participate in internal and external audits.</li>
<li>Interface with partners on quality topics.</li>
<li>Evaluate and approve proposed design or manufacturing process change.</li>
<li>Drive system and process improvements.</li>
<li>Manage Suppliers and Supplier Qualifications per applicable Millyard supplier quality procedures.</li>
<li>Manage the Supplier Corrective and Preventive Action requests.</li>
<li>Facilitate the review and approval of supplier-initiated changes and communicate the approved changes to the appropriate departments. </li>
</ul>
To be successful in this role, you will need the following skills &amp; experience: 
<ul>
<li>Bachelor’s degree in an engineering or related STEM discipline. Additional training and experience may be considered in lieu of degree.</li>
<li>Minimum 5 years' experience in any suitable occupation related to quality assurance of medical devices.</li>
<li>Experience with medical devices and direct responsibility for Risk Analysis and Design Transfer required.</li>
<li>Experience with compliance, applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 required.</li>
<li>Experience developing and leading quality system procedures required.</li>
<li>Experience supporting regulatory body submissions preferred.</li>
<li>Experience participating in internal and external audits preferred.</li>
<li>Hands-on experience in Supplier Qualification, Supplier Audits, and Supplier Corrective Action.</li>
<li>Ability to:</li>
<ul>
<li>Multitask and carry tasks through to completion.</li>
<li>Manage multiple sources of data and develop reports.</li>
</ul>
</ul>

Senior Quality Engineer - medical device

<h3>Job Description</h3>
Job Description
Position Summary
TheSenior Process Engineer is responsible for designing, developing, optimizing and troubleshooting manufacturing processes in a manner that meets safety, quality and operational performance expectations. This position provides leadership and creativity in the formulation development, process development and optimization, scale up and manufacturing. The key function of this role is to identify and solve problems in the manufacturing process transfer and scale up, and deliver effective, safe and efficient manufacturing processes for parenteral drug products. The Senior Process Engineer is hands-on, able to handle multiple tasks with sound planning and communication and providing training and support to peers. 
Duties and Responsibilities










 
<ul>
<li>Analyze organic or inorganic pharmaceutical excipients to determine chemical or physical compatibilities with active drug molecules for the development of stable pharmaceutical product </li>
<li>Evaluate changes in the composition/stability of pharmaceutical products due to changes in variables such as heat, light, or chemical catalysts for quantitative or qualitative analysis</li>
<li>Propose and prepare formulations with different excipients or solvents to conduct experiments and analytical testing at laboratory scale</li>
<li>Propose and develop lyophilization product and process or other complex formulation process such as liposome, TFF and viscous product</li>
<li>Take an active part in scale-up and technology transfer of newly developed products from R&amp;D to manufacturing</li>
<li>Identify and order materials required to perform development and manufacturing</li>
<li>Identify tooling and equipment required to perform development and manufacturing</li>
<li>Create documents for laboratory/manufacturing operations and quality such as master batch records, study protocols, engineering batch record, process characterization reports, standard operating procedures (SOP), etc. Review these documents for their compliance with cGMP and FDA standards</li>
<li>Due diligence on manufacturing process design and risk analysis to ensure operation safety, efficiency and quality</li>
<li>Propose testing procedures for analyzing CQA and coordinate with quality control testing to ensure the quality of finished drug product</li>
<li>Compile and analyze test information to determine process or equipment operating efficiency or to diagnose malfunctions</li>
<li>Analyze in-process and release testing results to design, analyze, and control pharmaceutical manufacturing processes through the measurement of critical process parameters (CPP) which affect the critical quality attributes (CQA) of the pharmaceutical product</li>
<li>Maintain ownership of assigned laboratory instruments to ensure proper working order and troubleshoot malfunctions when needed</li>
<li>Study effects of various manufacturing techniques or packaging configuration on the composition or stability of pharmaceutical product</li>
<li>Develop, improve or customize equipment, formulas, processes or analytical methods to maintain quality of pharmaceutical product</li>
<li>Write technical papers or reports or prepare standards and specifications for processes, facilities, products, or tests</li>
<li>Carry out all job responsibilities in a safe manner</li>
<li>Develop equipment and processes that meet safety codes, policies and guidelines</li>
<li>Provide for the safety and well-being of operators, maintenance, and other personnel</li>
<li>Confer with scientists or engineers to conduct analyses of research projects, interpret test results or develop procedure and standard tests</li>
<li>Other duties as assigned</li>
</ul>
Regulatory Responsibilities 
<ul>
<li>Conduct business in a responsible manner that complies with all state, FDA, OSHA, EPA, and DEP regulations, or otherwise as applicable</li>
<li>Provide leadership in daily operations, and have employees incorporate these compliance practices into their daily routines</li>
</ul>
Supervisory Responsibilities
<ul>
<li>Lead/support validation activities including equipment validation and process validation</li>
<li>Lead problem solving and investigate quality events related to formulation process or batch records</li>
<li>Propose and lead process improvement initiatives to improve operating performance and laboratory safety procedures to ensure compliance with the cGMP and FDA standards</li>
<li>Lead or participate in root cause analysis and quality event investigation such as OOS and deviations</li>
<li>Supervise, mentor and develop team members or relevant personnel across departments</li>
</ul>
Experience
<ul>
<li>A minimum of three (3) years of experience in pharmaceutical research and manufacturing</li>
</ul>
Education
<ul>
<li>Bachelor’s degree or above in Chemical Engineering, Chemistry, Biology or Pharmaceutical Science </li>
</ul>
Knowledge, Skills &amp; Abilities
<ul>
<li>Experience in sterile manufacturing is preferred</li>
<li>Experience in lyophilization and terminal sterilization techniques are a plus</li>
<li>Knowledge of parenteral drug product manufacturing</li>
<li>Proficient with calculation, data analysis, statistics and applied mathematics</li>
<li>Exceptional computer skills including Microsoft Office, Visio or other related software</li>
<li>Excellent writing skills</li>
<li>Attention to detail</li>
</ul>
Physical Requirements

<ul>
<li>Ability to sit for prolonged periods of time</li>
<li>Ability to stand for prolonged periods of time</li>
<li>Able to lift up to 50lbs</li>
</ul>

Senior Process Engineer

<h3>Job Description</h3>
Job DescriptionRange Commercial Partners, Inc. is hiring a Building Maintenance Engineer in Chelsea, MA! Range Commercial Partners was founded by seasoned experts in sales, leasing, property management, and development, who united around common goals and principles. Independently owned, we operate with open minds, no geographic constraints, and unwavering commitment to success for our clients and our firm. Driven, generous, and mindful of balance, we’re forming teams that are built to make a difference!&nbsp; What you will be doing:
<ul>
<li>Inspect building systems including fire alarms, HVAC, electrical, and plumbing to ensure operation of equipment is within design capabilities and achieves environmental conditions prescribed by client at assigned properties.</li>
<li>Performs day to day repairs, emergency maintenance, and preventive maintenance on all assigned properties or accounts including daily housekeeping chores.</li>
<li>Assists with troubleshooting and repairs of buildings and installed systems to include: plumbing systems, kitchen equipment, roofs, drains, shop, and HVAC.&nbsp;</li>
<li>Receives and completes work orders for corrective repair work on a variety of building physical structures, equipment, and system components in a timely manner as assigned.</li>
<li>Oversees and inspects the work performed by outside contractors.</li>
<li>Maintains lighting systems throughout the facility, cleaning fixtures and replacing bulbs and lamps.</li>
<li>Orders necessary materials in order to complete all required repairs, within limits set by the Property Manager.</li>
<li>Completes all required paperwork within established deadlines to close out work orders.</li>
<li>Maintains and renews any required trade certifications and licenses.</li>
<li>Periodically, meets with the assigned Property Manager to ensure that all aspects of required or requested maintenance work are achieving the goals and objectives established to maintain the property.</li>
<li>Ensures that requests for work that exceed routine day to day repairs or maintenance, is properly referred and routed to the Chief Engineer for review.</li>
<li>Is responsible for 24/7 vehicle readiness as a part of the maintenance position.</li>
<li>Promptly reports unusual events or conditions discovered on assigned properties to the Property Manager and the Maintenance Supervisor.</li>
<li>Performs work in accordance with all Federal and State OSHA guidelines and requirements.</li>
<li>Physical requirements include stooping, standing, walking, climbing stairs/ ladders, and ability to lift/carry heavy loads of 50 lbs. or more.</li>
</ul>
What you will bring along:
<ul>
<li>High school education.</li>
<li>Advanced knowledge of plumbing, electrical, mechanical, roofing, drywall, carpentry, and HVAC troubleshooting.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Strong organizational and analytical skills.</li>
<li>Ability to provide efficient, timely, reliable and courteous service to customers, with the ability to present information.</li>
<li>Requires knowledge of financial terms and principles to understand operating budgets.</li>
<li>Ability to comprehend, analyze and interpret documents.</li>
<li>Ability to solve problems involving several options in situations that require intermediate analytical and quantitative skills.</li>
<li>Uses computer and phone for work order system, email, and training. Basic skills with Microsoft Office Outlook.</li>
<li>Decisions made with thorough knowledge of procedures and company policies to achieve set results and deadlines. Responsible for setting own project deadlines.</li>
<li>Must always use professional judgement and decisions made with thorough understanding of procedures, company policies, and business practices to achieve general results and deadlines.</li>
<li>Ability to work in a fast-paced environment and will need to be able to adapt to shift priorities efficiently and effectively.</li>
<li>Excellent collaboration and written and verbal communication skills required to effectively communicate with diverse populations are essential.</li>
<li>Embrace the Range Commercial Partners values:
<ul>
<li>Service</li>
<li>Excellence</li>
<li>Respect</li>
<li>Versatility</li>
<li>Integrity</li>
<li>Curiosity</li>
<li>Efficiency</li>
</ul>
</li>
</ul>
The Perks:&nbsp;
<ul>
<li>Health coverage for you and your family through medical, dental and vision plans.</li>
<li>Financial protection through disability, life, and accidental death and dismemberment.</li>
<li>A 401(k) plan in which the company matches dollar for dollar on a generous % you contribute.</li>
<li>A generous paid time off program in which the benefits increase along with your tenure with the company.</li>
<li>Bring your dog to work days.</li>
</ul>
Range Commercial Partners, Inc. is proud to be an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
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90fciP84oO

Building Maintenance Engineer

<h3>Job Description</h3>
Job Description
InnoTECH Staffing is looking for an experienced Mechanical Design Engineer to participate in the development of innovative medical devices for a company located in the Manchester, NH area.
This position requires being onsite 5 days a week and must be a US Citizen or Greencard holder.
They Mechanical Engineer will work as part of a team driving products through their lifecycle including concept generation, prototyping, component and assembly development, testing, and associated documentation. The candidate is expected to be very self-sufficient in handling multiple sub-assembly designs simultaneously, requiring a very low level of guidance. The candidate must have excellent problem solving and analytical skills and be able to learn quickly in a dynamic, fast-paced environment. How you will make an impact: 
<ul>
<li>Generate creative solutions to design problems and demonstrate their viability considering factors such as risk, reliability, manufacturability, serviceability, weight and cost</li>
<li>Transition concepts into products using 3D CAD Solid Modeling, defining requirements, selecting materials and processes, interacting with suppliers and manufacturers, and documenting the development process</li>
<li>Troubleshoot design failure modes to root cause and develop quick, effective solutions</li>
<li>Coordinate with others in a multi-disciplinary team environment including electrical, software, industrial design, and controls</li>
<li>Evaluate designs through prototype testing and requirement verification</li>
<li>Technical review and approval for all mechanical component and assembly designs, analysis, and testing</li>
<li>Set an excellent example of mechanical engineering practices and provide a level of mentorship to less knowledgeable engineers. </li>
</ul>
To be successful in this role you will need to following skills and experience: 
<ul>
<li>Bachelor’s Degree in Mechanical or Manufacturing Engineering</li>
<li>Minimum of 5+ years’ experience with mechanical design for manufacturability in a high precision/high volume manufacturing environment (medical preferred)</li>
<li>1+ years’ experience with electro-mechanical devices with embedded software preferred</li>
<li>Familiarity with:</li>
<ul>
<li>Plastic injection molding required</li>
<li>Die casting preferred</li>
<li>Metal injection molding a plus</li>
</ul>
<li>Exposure to process validation and mold qualifications</li>
<li>Organizational and coordination skills with a detail-oriented mindset and ability to juggle multiple activities</li>
<li>High energy, drive, commitment, self-initiative, and perseverance to drive projects forward to completion</li>
<li>Exceptional verbal and written communication skills with the desire to work in a collaborative environment</li>
<li>Ability to communicate technically with a variety of engineering disciplines</li>
</ul>

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