We are looking for a Sr R&D Lab Technician – Disposables to work with our expert Cell and Gene Therapy Disposables Kit R&D team based in Marlborough, MA. Do you have a passion for cell therapy? Then we would love to hear from you.

We at Ian Martin envision a world where everyone is connected in meaningful work and if you find great meaning in developing some of the most widely used products in the world, then we have the career path for you.

What will you do?

•        Participate in the design and organization of experiments in conjunction with the Tech Lead and or R&D Team members. Serve as a resource to R&D Team.

•        Perform hands-on tests of new products in development. Prepare samples and execute tests, collaborating with colleagues as necessary to gain access and training. Record test data in accordance with GLP.

•        In addition to executing existing tests, you will also be expected to propose, design, improve, develop and/or implement new tests procedures for evaluating new product’s specifications within the verification and validation activities framework.

•        Contribute to the generation of work instructions, tests protocols, and reports.

•        Follow departmental work instructions, SOP’s, OSHA safety regulations and cGMPs & cGLPs to perform assigned tasks.

•        Monitor and oversee lab supply inventory, generate expense purchase requisitions, if applicable, and maintain documentation in accordance with established procedures.

•        Interface with internal groups to assure laboratory equipment maintenance, calibration and documents conform with established practices.

Knowledge, Skill or Ability:

•        Deep knowledge in medical device disposables (Class II), with relevant experience in developing tests methods, writing test protocols, and verifying product design specifications of new products.

•        Backgrounds in manufacturing process development related to medical device, disposables an asset (IQ, OQ, PQ, Process FMEA)

•        Basic knowledge of mechanical design of fixtures (CAD Design – SolidWorks)

•        Familiarity with the mechanical testing of plastic parts and sub-assemblies (e.g. tensile/shear/compression test, hardness measurement, pressure decay measurement, burst test) and product reliability tests (e.g. any tear/wear/aging test)

•        Ability to work under cGMP/cGLP guidelines

•        Strong communication, interpersonal skills, and the ability to work in a team environment are required.

•        Demonstrate strong ethical behavior

•        Detail-oriented, and able to work independently as well as part of a team

•        Possess good computer skills (Microsoft Office is required. Word, Excel)

Must have:

We are looking more for a candidate with associate degree in Engineering Technology, Mechanical Engineering or Materials Science with exposure to Medical Device Industry and plastics products as disposables and experience with mechanical lab tests as described in the job desk.

Education:

•        Minimum (required): Associates Degree in Technology or Engineering

•        Equivalent combination of education and work experience

Looking for Meaningful Work? We can help.

If you are a Project Manager, you know that it can be difficult to find fulfilling work that advances your career. At the Ian Martin Group, we exist to connect professionals like you with meaningful work at industry-leading companies in your field. And we walk the walk, too: as a Certified B Corporation, we believe in using business as a force for good for people, our communities, and the environment.

We value diversity and inclusion and encourage all qualified people to apply. If we can make this easier through accommodation in the recruitment process, please contact us at recruit@ianmartin.com.

We encourage all qualified candidates to apply; however, only those selected for an interview will be contacted.

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We are looking for a EHS Specialist for our American multinational conglomerate company in Westborough, MA for a contract opportunity.

Our Client is a manufacturer and distributor of diagnostic imaging agents and radiopharmaceuticals for imaging modalities that are used in medical imaging procedures

We at Ian Martin envision a world where everyone is connected in meaningful work and if you find great meaning in developing some of the most widely used products in the world, then we have the career path for you.

On day to day basis:

This position is responsible for conducting Environmental Health and Safety (EHS) activities, under the direction and supervision of the site EHS leader. The primary focus is to conduct site-wide and department area EHS inspections including for hazardous waste storage areas, support site emergency response activities, conduct & follow up on employee injury & other incident investigations, maintain EHS recordkeeping systems, conduct or assist with EHS employee site trainings, and participate in other EHS program activities to ensure employee safety and regulatory compliance in the manufacturing environment. Specifically, workers that directly or indirectly support services that are invoiced to client through one of several contractual arrangements (e.g., time/materials, statement of work, purchase agreement, direct labor).

Education:

A College student who is working toward a 4 year environmental or safety degree would be awesome. I guess to relate that to more traditional terms minimum associates degree. Ideally in an environmental or safety discipline.

Shifts:

There are multiple 2nd and 3rd shift work schedules as each of the 4 major departments have a different schedule. Some start at 2:30 or 3:30 or 4:30 pm, and either end at 12:30 am, 2:30 or 3:30 am. And FYI, one department starts their first shift at 4:30 am.

So, for this EHS Specialist role, we primarily want someone to accommodate most of the evening hours by starting late afternoon. Also, open tomorrow someone starting as early as 3 pm and working thru 12 am (9 hours per day).

In addition, we will start this new person for their first 2 weeks during day shift hours so they can be properly trained before starting their night shift hours.

Looking for Meaningful Work? We can help.

If you are a EHS Specialist, you know that it can be difficult to find fulfilling work that advances your career. At the Ian Martin Group, we exist to connect professionals like you with meaningful work at industry-leading companies in your field. And we walk the walk, too: as a Certified B Corporation, we believe in using business as a force for good for people, our communities, and the environment.

We value diversity and inclusion and encourage all qualified people to apply. If we can make this easier through accommodation in the recruitment process, please contact us at recruit@ianmartin.com.

We encourage all qualified candidates to apply; however, only those selected for an interview will be contacted.

#MON

#EWEMi

Our Global Life Sciences client is currently looking for a Quality Assurance Analyst who will be responsible for providing manufacturing and/or engineering process support in accordance with documented procedures and practices in Marlborough, MA.

We at Ian Martin envision a world where everyone is connected in meaningful work and if you find great meaning in developing some of the most widely used products in the world, then we have the career path for you.

Role Summary/Purpose

This position is responsible for providing manufacturing and/or engineering process support in accordance with documented procedures and practices. This is a key technical role responsible for the development, implementation, improvement, and continuous reinforcement of established Quality Assurance fundamental practices that are utilized in the local business. The role involves hands-on work in the areas of design, design transfer, manufacturing, distribution, and/or service.

Qualifications/Requirements

·        Min of 3-year experience working in a regulated industry

·        Experience in a pharmaceutical industry

·        Experience with CAPA systems, Deviations, Nonconformance

·        Experience applying regulations (including FDA cGMP)

·        Ability to communicate effectively (both written and oral) in English

Desired Characteristics

·        Minimum of 3 years’ experience in a regulated industry is preferred

·        Demonstrated understanding or aptitude to understand Pharmaceutical QMS requirements and regulatory requirements including but not limited to FDA 21CFR 210, 211 and ICH Q10

·        Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies & in-depth understanding of site level products & related processes

·        Demonstrated expertise to effectively communicate within all levels of the organization around concepts of design controls, design verification and validation activities; production & process controls;

·        Corrective & Preventative Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc.

·        Demonstrated collaboration, negotiation & conflict resolution skills

Looking for Meaningful Work? We can help.

If you are a Quality Assurance Analyst, you know that it can be difficult to find fulfilling work that advances your career. At the Ian Martin Group, we exist to connect professionals like you with meaningful work at industry-leading companies in your field. And we walk the walk, too: as a Certified B Corporation, we believe in using business as a force for good for people, our communities, and the environment.

We value diversity and inclusion and encourage all qualified people to apply. If we can make this easier through accommodation in the recruitment process, please contact us at recruit@ianmartin.com.

We encourage all qualified candidates to apply; however, only those selected for an interview will be contacted.

#MON

#EWEMI