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<h3>Job Description</h3>
Job Description
Job Title: Bench Chemist
Job Description
We are seeking a skilled Bench Chemist to join our dynamic team. The ideal candidate will perform a variety of chemical analyses and support laboratory operations. The role involves working with raw materials, in-process samples, and finished goods using advanced testing methods.
Responsibilities
<ul>
<li>Run LC and GC testing of raw materials, in-process samples, and finished goods.</li>
<li>Prepare samples across matrices, run calibration curves, and conduct system suitability and integration review.</li>
<li>Perform wet chemistry techniques such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument care, including column maintenance, addressing leaks, and replacing pump seals, while adhering to IQ/OQ/PQ guidelines.</li>
<li>Provide basic troubleshooting and maintenance for laboratory instruments.</li>
<li>Support method validation work focusing on accuracy, precision, and limits of detection (LOD) and quantification (LOQ).</li>
<li>Flexibly support laboratory needs, including inventory management, lab clean-up, and peer review of notebooks.</li>
<li>Draft and review standard operating procedures (SOPs).</li>
</ul>
Essential Skills
<ul>
<li>Master's degree in Chemistry or Analytical Chemistry with 3-5 years of experience in a quality control laboratory, preferably in the food or supplement industry.</li>
<li>Proven ability to operate HPLC and GC independently.</li>
<li>Experience with natural product or lipid-rich matrices, focusing on small molecule testing such as vitamins, fats, emulsifiers, and actives.</li>
<li>Working knowledge of USP/AOAC methods and cGMP documentation.</li>
<li>Proficiency with chromatography software such as OpenLab and ChemStation.</li>
<li>Strong laboratory safety mindset and approach to work.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or Analytical Chemistry with 3-5 years of relevant laboratory experience.</li>
<li>wet chemistry, organic chemistry, formulation, and research &amp; development.</li>
</ul>
Work Environment
The position is based in a laboratory environment with a standard work schedule of Monday to Friday, from 8 AM to 5 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, Massachusetts.
Pay and Benefits
The pay range for this position is $40.00 - $40.00/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 &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;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 Hadley,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Bench Chemist - Food

<h3>Job Description</h3>
Job Descriptionjob summary: 
This role as a Quality Control Associate I, Microbiology in Norwood, MA, is a fantastic opportunity for a detail-oriented individual with a STEM degree and 6 months to 2 years of GMP QC microbiology experience.
You will be the key player in Environmental Monitoring (EM) and Critical Utilities sampling (WFI, Compressed Gas), ensuring the cleanroom environment is compliant. The position requires strong hands-on skills with equipment like particle counters and viable air samplers, combined with the ability to manage data using LIMS and other electronic databases. If you are proficient in GMP, microbiology, and aseptic techniques, and are ready to apply your troubleshooting skills to support critical quality systems, this contract role offers vital experience in a regulated setting.
Shifts: 
1 st Shift: Wednesday through Saturday, 7am-5pm
2 nd Shift: Wednesday through Saturday, 10am-8pm
2 nd Shift: Sunday through Wednesday, 10am-8pm
 location: Norwood, Massachusetts job type: Contract salary: $30 - 37 per hour work hours: 11 to 7 education: Bachelors responsibilities: 
<ul>
<li>Conduct Environmental Monitoring (Routine, In-Process, and EMPQ's), WFI Sampling, and Compressed Gas Sampling.</li>
<li>Maintain lab equipment and perform housekeeping tasks.</li>
<li>Write, revise, and follow SOPs, protocols, and reports.</li>
<li>Ensure data entry, review, and trending are performed using LIMS.</li>
<li>Collaborate with internal and external labs for sample coordination and testing.</li>
<li>Troubleshoot equipment and test methods.</li>
<li>Support quality systems records such as deviations, change controls, and CAPAs.</li>
<li>Participate in audits and continuous improvement initiatives.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>STEM degree with 6 months - 2 years of experience in a GMP QC laboratory setting, focusing on microbiology.</li>
<li>Hands-on experience with particle counters, viable air samplers, and gas equipment. </li>
<li>Proficiency with Microsoft Office Programs and electronic databases (LIMS, SAP, eQMS).</li>
<li>Excellent troubleshooting skills and the ability to communicate scientific issues clearly.</li>
<li>Knowledge of GMP, microbiology, aseptic techniques, and general laboratory instrumentation.</li>
<li>Familiarity with relevant FDA, EU, ICH guidelines, and regulations.</li>
</ul>
#LI-KH1
 skills: Quality control, SOP, FDA, MS-WORD, MS-EXCEL, Microbiology, ICH Regulations, GMP (Good Manufacturing Practice), Environmental Sampling, LIMS (Laboratory Information Management System 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. 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.

QC Microbiology Associate I

<h3>Job Description</h3>
Job Description
Nanobiosym is an innovative company in Cambridge, MA that is developing novel technologies to address a broad range of diseases. Nanobiosym was founded by an MIT/Harvard alum to work at the interface of physics, nanotechnology, and biomedicine. This hypergrowth company allows for unique career opportunities with strong long-term incentives. Nanobiosym is currently seeking top notch candidates to help the company scale up its operations.
 
Nanobiosym is looking for a General Supervisor for its High-Complexity Testing CLIA LAB. The role and requirements are below. The purpose of the Laboratory General Supervisor is to serve as a general supervisor under CLIA 42 CFR 493.1449 regulations for a molecular diagnostics lab. You will assist the Clinical Laboratory Director in day-to-day personnel, workflow, quality control, and equipment management. You are responsible for ensuring that the tests meet all regulatory requirements and coordinating with the laboratory staff to review data for accuracy and issue tests reports in a timely manner. 
 
Job Responsibilities:
<ol>
<li>Provide leadership and directs a team of technologists through positive communication and support </li>
<li>Train new personnel with regard to technical and operational procedures </li>
<li>Ensure all laboratory members are proficient in assay processing including biannual (first year and subsequent annual competency training) </li>
<li>Organize specimens required to be run </li>
<li>Review data for concordant analysis, write-up results, and file data with the assay tested under competency runs </li>
<li>Annually evaluate and document the performance of all testing personnel </li>
<li>Create daily/weekly technologist schedule for molecular diagnostic assays </li>
<li>Setting-up equipment and resources for the laboratory </li>
<li>Monitor examinations to ensure that acceptable levels of analytic performance are maintained and meet TATs </li>
<li>Ensure that all remedial actions are taken whenever test systems deviate from the laboratory's established performance specification </li>
<li>Report quality issues directly to the Clinical Laboratory Director </li>
<li>Track proficiency testing for the validated assay in the laboratory that includes calendar tracking, and following through concordance analysis and finalizing all documents in the database for any future inspections </li>
<li>Maintain all Quality Management System on instrument maintenance programs, i.e. preventative maintenance, cleanliness and maintains records of service in compliance CAP </li>
<li>Maintain and manage daily performance and workload distributed throughout the laboratory </li>
<li>Review issues regarding problem cases with Clinical Laboratory Director to get direction for troubleshooting and next step directions </li>
<li>Work with the lab team to monitor and maintain inventory of supplies, place orders of materials </li>
<li>Participate with Clinical Laboratory Director in managing all governmental and regulatory audits </li>
<li>Mange and monitor Quality Control (QC), Quality Assurance (QA), Safety and Inspection practices to assure compliance with CLIA and MA regulations </li>
<li>Develop, implement and maintain SOPs as per CLIA and MA regulation </li>
<li>Maintain a flexible schedule to meet laboratory goals</li>
</ol>
 
Qualifications:
<ol>
<li>Qualified as a Director for high-complexity testing; </li>
<li>OR Qualified as a Technical Supervisor for high complexity testing; </li>
<li>OR Doctoral degree in clinical laboratory science or chemical, physical or biological science with 1 year training and experience in high-complexity testing; </li>
<li>OR Master's degree in clinical laboratory science, medical technology or chemical, physical or biological science and 1 year training and experience in high-complexity testing; </li>
<li>OR Bachelor's degree in clinical laboratory science, medical technology or chemical, physical or biological science and 1 year training and experience in high-complexity testing;</li>
<li>OR Associate degree in medical laboratory technology (or pulmonary function) and 2 years laboratory (or blood gas analysis) training or experience, or both, in high complexity testing Refer to the CLIA regulation 42CFR493.1461 for additional qualifications </li>
</ol>
 Job Posted by ApplicantPro

General Supervisor for High Complexity CLIA LAB

<h3>Job Description</h3>
Job Description
At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands—including Curaleaf, Select, and Grassroots—offer premium products and services in both medical and adult-use markets.
Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our Rooted in Good initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis.
Lab Processing Supervisor- 2nd Shift
Job Type: Full Time, Exempt Shifts: 3:30pm-11:30pm M-F Salary Range: 57k - 69k + bonus Location: Webster, MA
POSITION SUMMARY:
The Processing Lab Supervisor will supervise and optimize all the tasks in the Post Processing Lab and will assist the Lab Manager and Manufacturing team by maintaining quality control measures in the extraction and purification processes and thereby ensuring the delivery of high-quality product. This Supervisor carries out day-to-day tasks including prepping for distillation runs, formulations, and Ethanol extractions, and maintaining paperwork using good documentation practices. The Laboratory Supervisor will be a hands-on working supervisor responsible for extraction team training and schedule coordination between early and late overlapping shifts.  
ESSENTIAL DUTIES AND RESPONSIBILITIES:
<ul>
<li>Directly supervises the Post Processing staff and accomplishes department results by communicating job expectations; weekly and monthly planning; monitoring, and appraising job results; coaching, counseling, and disciplining employees; initiating, coordinating, and enforcing systems, policies, and procedures. </li>
</ul>
<ul>
<li>This position and all output metrics report directly to the Lab Manager. These reports will include all daily production metrics, establishing actual vs. expected production results with explanations of variances, staff absences and all associated production paperwork. </li>
</ul>
<ul>
<li>Shows the capability to effectively communicate with management and co-workers on a professional basis. This will include all team members, leads, supervisors, and upper management. </li>
</ul>
<ul>
<li>Preparing for efficient production by reviewing the manufacturing schedule; studying and clarifying specifications; calculating batch requirements; assembling and weighing plant materials and supplies for extractions, distillations and formulations. </li>
</ul>
<ul>
<li>Ensure proper scheduling of Post Processing team, accounting for PTO and call offs when applicable. </li>
</ul>
<ul>
<li>Performing all training required for Post Processing team, including maintaining all required documentation. </li>
</ul>
<ul>
<li>Operating highly sophisticated extraction and processing equipment; Processing concentrate, extracts and formulated products. </li>
</ul>
<ul>
<li>Cleaning and maintaining lab equipment and laboratory facility following current good manufacturing practices (cGMP), and standard operating procedures; complying with legal regulations. </li>
</ul>
<ul>
<li>Operating, maintaining, adjusting, trouble shooting, and repairing laboratory equipment such as extractors, heaters, chillers, vacuum pumps, balances, centrifuges, distillation units and other laboratory equipment. </li>
</ul>
<ul>
<li>Operating extraction equipment to extract crude oil utilizing Ethanol as a solvent in a C1D2 environment. </li>
</ul>
<ul>
<li>Operating highly sophisticated purification equipment to convert crude oil into decarboxylated oil. </li>
</ul>
<ul>
<li>Following procedures for extract purification, including ethanol addition, winterization, filtration, rotary evaporation, decarboxylation and distillation. </li>
</ul>
<ul>
<li>Assisting with the development of further purification processes and in-process materials, including processes for new products. </li>
</ul>
<ul>
<li>Maintaining inventory records of supplies, materials, equipment PMs as required, and preparing requisitions as needed. </li>
</ul>
<ul>
<li>Maintaining strict inventory within state-issued cannabis inventory software, MJ Freeway, via regular cycle counts of WIP inventory. </li>
</ul>
<ul>
<li>Storing supplies and equipment, disposing of waste according to state guidelines, and keeping laboratory, storerooms and working areas organized. </li>
</ul>
<ul>
<li>Performing clerical work related to laboratory activities such as word processing, record keeping, data logging and filing. </li>
</ul>
<ul>
<li>Maintaining material safety data sheets for all department chemicals and products. </li>
</ul>
<ul>
<li>Performing related duties as assigned </li>
</ul>
<ul>
<li>Perform other duties as assigned. </li>
</ul>
Supervisory Responsibilities: 
This position directly supervises the work activities of others and makes recommendations concerning selection, termination, performance appraisal, and professional development 
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. 
Minimum Qualifications: 
<ul>
<li>BS/BA Degree or greater in Chemistry, Bio-Chemistry or similar. </li>
</ul>
<ul>
<li>Minimum of 2 years' experience in a lab or manufacturing setting. </li>
</ul>
<ul>
<li>Minimum of 2 years' experience leading and managing a team. </li>
</ul>
<ul>
<li>Experience with scientific writing for processes, training, and procedures that require documentation </li>
</ul>
<ul>
<li>Knowledge of and hands-on experience with Ethanol Extraction, Winterization &amp; Filtration, Rotary Evaporation, Distillations and Product Formulations. </li>
</ul>
<ul>
<li>Ability to draft weekly and monthly schedule for department processes, as well as establish daily metrics for each process on a week by week basis. </li>
</ul>
<ul>
<li>Ability to Follow health and safety practices and precautions applicable to an extraction laboratory </li>
</ul>
<ul>
<li>Experience with proper and safe handling and disposal of harmful chemicals, substances, and hazardous wastes </li>
</ul>
<ul>
<li>Experience with computer systems, software, and hardware common to laboratories </li>
</ul>
<ul>
<li>Experience with record keeping procedures, as well as regular audits of team's production sheets to ensure accuracy and completeness. </li>
</ul>
Preferred Qualifications: 
<ul>
<li>1-year experience in the cannabis industry preferred </li>
</ul>
<ul>
<li>QA/QC experience with HPLC and GC analysis preferred but not required. </li>
</ul>
Physical Requirements: 
<ul>
<li>Must be able to stand for prolonged periods of time, along with frequent bending </li>
<li>Close vision (unobstructed vision at 20 inches or less) </li>
<li>Manual dexterity sufficient to reach/handle items, work with fingers </li>
<li>Ability to lift to 50 pounds and push up to 100 pounds with assistance </li>
</ul>
Massachusetts Hiring Range$57,000—$69,000 USD
What We Offer:
<ul>
<li>Career Growth Opportunities</li>
<li>Competitive Pay and Benefits</li>
<li>Generous PTO and Parental Leave</li>
<li>401(K) Retirement Plan</li>
<li>Life/ Disability Insurance</li>
<li>Community Involvement</li>
<li>Referral Bonuses and Product Discounts</li>
</ul>
Benefits vary by state, role type, and eligibility. 
Follow us on Social Media: Instagram: @curaleaf.usa Twitter: @Curaleaf_Inc LinkedIn: Curaleaf LinkedIn
Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence
Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis. 
Our Values:
<ul>
<li>Lead and Inspire. </li>
<li>Commit to Win. </li>
<li>ONE Curaleaf. </li>
<li>Driven to Deliver Excellence. </li>
</ul>
Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Individuals adversely impacted by the war on drugs are encouraged to apply.
Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.

Lab Processing Supervisor

<h3>Job Description</h3>
Job DescriptionDescription:
Hoyle Tanner is seeking a part-time Geotechnical Engineer for our Ground Transportation Services Division. If you have a PE license and 10 years of experience, we would like to offer you a role in design and analysis of infrastructure projects from bridge foundations, retaining walls, treatment plan structures. A perfect opportunity for the retired Engineer who is looking for a part-time project.
We are a welcoming, collaborative, respectful, encouraging, and diverse community where you can achieve your career goals. Our midsize allows you to be visible and heard. Hoyle Tanner offers you a flexible schedule, remote work opportunities and a generous sign-on bonus. See our impressive benefits package for more information.
 
Location: Chelmsford, MA
A short 27 miles from Boston, our office is centrally located just south of the confluence of US Route 3, Route 495, and the Lowell Connector, with a stop along the MBTA’s Lowell bus route 15, and a short drive from the Lowell and Billerica commuter rail stops. This office is located along the developing Route 129 corridor in Chelmsford.
 
Responsibilities include:
<ul>
<li>Develop geotechnical investigation requirements for projects and develop scopes of services and budgets for sub-consultant partners including other geotechnical specialists or subsurface investigation companies</li>
<li>Interface with sub-consultant geotechnical engineering firms or subsurface investigation companies to coordinate services and review submissions</li>
<li>Perform fieldwork, as necessary, to subsurface investigation parameters or to observe investigations</li>
<li>Perform/ review design calculations for project components such as abutments, walls, foundations, retaining walls, and tanks</li>
<li>Assist with design of airfield pavements and present alternative pavement solutions that may provide project sustainability and resilience benefits</li>
<li>Mentor team members on aspects of geotechnical engineering including interpretation of subsurface data and designs of civil infrastructure components</li>
<li>Design and evaluate shallow and deep foundation systems including driven piles, micro-piles, integral abutments, reinforced earth structures, and other geotechnical engineering solutions</li>
<li>Prepare geotechnical reports, design calculations, and construction specifications</li>
<li>Collaborate with project managers and other technical team members to ensure the successful completion of projects by communicating the integration of geotechnical investigations into design projects</li>
<li>Perform site visits and inspections to assess soil conditions, evaluate foundation performance, and provide recommendations for rehabilitation</li>
<li>Stay current with industry standards, codes, and regulations related to geotechnical engineering</li>
<li>Participate in project meetings and communicate effectively with clients, contractors, and regulatory agencies</li>
</ul>
Benefits:
<ul>
<li>Competitive salary aligning with experience</li>
<li>Flexible hours and opportunity for a hybrid work environment</li>
<li>Flexibility to work part or full time</li>
<li>Opportunities for professional development and continuing education</li>
<li>Comprehensive benefits package including health insurance, retirement plans and paid time off</li>
<li>Collaborative and supportive work environment</li>
</ul>
Requirements:
Qualifications:
<ul>
<li>BS in Civil Engineering (MS in Geotechnical Engineering preferred)</li>
<li>Professional Engineer (PE) licensure required</li>
<li>Minimum of 10 years' experience in geotechnical engineering, with a focus on the design of bridge foundations, retaining walls, treatment plant structures, and/ or facility foundations</li>
<li>Proficiency in the design and analysis of shallow and deep foundations including driven piles, micro-piles, integral abutments, and reinforced earth structures</li>
<li>Strong understanding of geotechnical engineering principles, soil mechanics, and foundation design</li>
<li>Experience with related geotechnical software, such as LPile, or other similar tools and industry-related applications</li>
<li>Strong communication and interpersonal skills, with the ability to work effectively in a team environment as well as the ability to work independently</li>
<li>Strong problem-solving skills and attention to detail</li>
<li>Salary is contingent on experience</li>
</ul>
Hoyle Tanner is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Hoyle Tanner does not currently offer sponsorship and participates in E-Verify. All offers are contingent upon a successful criminal background check.

Geotechnical Engineer - Chelmsford, MA

<h3>Job Description</h3>
Job DescriptionToday, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
We are thrilled to announce an outstanding opportunity for a Senior Biotechnologist at Lonza AG, based in New Hampshire, USA. As one of the world's largest healthcare manufacturing organizations, Lonza is committed to encouraging a safe, controlled work environment and promoting continuous growth. The Senior Biotechnologist will play a vital role in ensuring the outstanding implementation of our daring projects within the Cell Gene Therapy network.
Key responsibilities:
<ul>
<li>
Ensure site safety objectives are strictly communicated and understood.
</li>
<li>
Demonstrate flexibility by supporting other sites within the Cell Gene Therapy network, including necessary travel.
</li>
<li>
Act as the Subject Matter Expert in the assigned area (e.g., Cell Growth, Drug Product Filling) during manufacturing operations.
</li>
<li>
Assume a lead role during manufacturing operations such as harvest, vial filling, and visual inspection.
</li>
<li>
Collaborate with customer SMEs to successfully implement and maintain customers' processes in the production facility.
</li>
<li>
Represent manufacturing in technical and project meetings during campaign preparation.
</li>
<li>
Provide and arrange effective training for manufacturing staff on new processes, batch records, or quality systems used in Cell Therapy.
</li>
<li>
Work with the CT Manufacturing project specialist team to incorporate process and operational improvements into new customer processes.
</li>
<li>
Collaborate with the CT Manufacturing team to determine and procure necessary equipment and materials for process execution.
</li>
</ul>
Key requirements:
<ul>
<li>
High School Diploma or equivalent experience is required; a bachelor’s degree or equivalent experience is preferred.
</li>
<li>
5-10 years of proven experience in a related field.
</li>
<li>
Outstanding communication and collaboration skills.
</li>
<li>
Strong ability to compete and thrive in a fast-paced, dynamic environment.
</li>
<li>
Demonstrated ability to successfully coordinate and lead all aspects of complex biotechnological processes.
</li>
<li>
Proven track record of leadership and expertise in relevant manufacturing areas.
</li>
<li>
Willingness to travel and support other manufacturing sites as needed.
</li>
</ul>
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
]]&gt;

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