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<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Manager of Microbiology is responsible for the day-to-day and strategic functions of the QC Microbiology and Microbiology- Validation groups in Salem, NH. The Manager is responsible for providing technical support, scheduling and prioritizing work to meet customer expectations, and ensuring all work is performed in compliance with the quality, health, and safety objectives of the company. Provide technical support to Microbiologists and Client Services team members as needed. Responsible for all aspects of staff management including training, hiring, conducting feedback sessions, employee development, retention and engagement, disciplinary actions, and terminations. The Manager has direct responsibility for improving production efficiency and helping to meet the financial goals of the Microbiology department.
The essential duties and responsibilities of this position include the following. Other duties may be assigned as needed.
 
PRIMARY DUTIES AND RESPONISIBITIES
<ul>
<li>Leads the development and implementation of process improvement initiatives that promote increased productivity for the QC Micro and Validation groups.</li>
<li>Coordinates work projects to appropriately prioritize laboratory workload to meet client requirements as related to quality, on-time performance and TAT (Turnaround Time).</li>
<li>Distributes work to staff in order to maximize productivity.</li>
<li>Maintains quality performance metrics, conducts routine metrics review and root cause analysis in collaboration with the microbiologists.</li>
<li>Devises and develops processes and methods for the solution of technical problems.</li>
<li>Trains, mentors and supervises staff on an as needed basis.</li>
<li>Confers with Quality Assurance and Microbiology Director to design and/or improve standard operating procedures and/or training programs.</li>
<li>Responsible for scheduling work in support of maintaining all deadlines.</li>
<li>Ensures that laboratory supplies, consumables, standards are available to perform the analyses within the required project turnaround time.</li>
<li>Communicates project delays, quality and or technical issues to the Microbiology Director, and/or Client Services/Sales Team, as needed.</li>
<li>Reviews lab nonconformance (investigation and deviations) with microbiologists. Conducts root cause analysis and implements solutions in collaboration with the team.</li>
<li>Manages all aspects of office and lab operations as related to operating costs.</li>
<li>Responsible for the interviewing and the hiring of employees.</li>
<li>Provides regular ongoing performance feedback while serving as a coach and mentor.</li>
<li>Responsible for developing and communicating goals to microbiologists.</li>
<li>Ensures all work is performed in compliance with Standard Operating Procedures, Good Manufacturing Practices, Regulations of the Food and Drug Administration, Company, Client and Pharmacopeial Methodologies.</li>
<li>Follows all safety rules and regulations.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Maintain a clean and orderly laboratory environment.</li>
<li>Proper handling of hazardous waste in compliance with the Company and hazardous waste rules.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a Masters and/or Bachelors degree in Microbiology or a related discipline is required. Must have laboratory experience with a minimum of 5 years of related work experience. Knowledge of cGMPs and related compliance regulations and guidances required.
Must have experience with the various products and services the Company offers including LIMS and ELN and Microbiology.
This position requires a self-starting, motivated person who possesses excellent interpersonal skills; who is able to assume a leadership role in the organization; and, who is able to effectively interact with all departments within the company and with client personnel.
 
MINIMUM SKILLS REQUIREMENT
<ul>
<li>Demonstrated skills in laboratory techniques.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Microbiology Manager

<h3>Job Description</h3>
Job Description
Head of Biologics MSAT
<ul>
<li>Can be based in Philadephlia or Boston</li>
</ul>
Position Summary: The head of Biologics MSAT will lead the strategic and operational oversight of the Manufacturing Science and Technology function for biologics DS and/or DP manufacturing. This role is responsible for ensuring robust technology transfer, process validation, lifecycle management, and continuous improvement of biologics manufacturing processes across internal and external manufacturing global sites. The ideal candidate will bring deep technical expertise in biologics (e.g., monoclonal antibodies, ADCs, dAbs, fusion proteins), strong leadership capabilities, and a proven track record of cross-functional collaboration.
Key Responsibilities:
<ul>
<li>Lead and develop a high-performing MSAT team supporting clinical and commercial biologics manufacturing.</li>
<li>Oversee technology transfer of biologics processes from development to manufacturing, ensuring scalability, robustness, and compliance.</li>
<li>Drive global process validation strategies in alignment with regulatory expectations (e.g., FDA, EMA, ICH).</li>
<li>Provide technical leadership for troubleshooting, deviation investigations, and CAPA implementation.</li>
<li>Partner with Quality, Regulatory, Development, and Manufacturing to ensure seamless product lifecycle management.</li>
<li>Lead initiatives for process optimization, cost reduction, and implementation of new technologies (e.g., PAT, automation, single-use systems).</li>
<li>Consistently acting and leading with personal accountability for the quality and compliance of the MSAT team and beyond.</li>
<li>Serve as a subject matter expert during regulatory inspections and audits.</li>
<li>Develop and manage MSAT budgets, resource planning, and strategic initiatives.</li>
<li>Foster a culture of innovation, scientific excellence, and continuous improvement.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. or M.S. in Biochemical Engineering, Biotechnology, or related field; Ph.D. preferred.</li>
<li>15+ years of experience in biologics manufacturing, with at least 7 years in a leadership role within MSAT or Technical Operations.</li>
<li>Deep understanding of scale-up, upstream &amp; downstream biologics processes, tech transfers, and regulatory requirements.</li>
<li>Experience with CMO/CRO management and global manufacturing networks.</li>
<li>Demonstrated success in leading cross-functional teams and managing complex projects.</li>
<li>Consistently acting and leading with personal accountability for the quality and compliance of the MSAT team and beyond.</li>
<li>Extensive experience in structured technical troubleshooting, RCA and CAPA effectiveness</li>
<li>Excellent communication, leadership, and strategic thinking skills.</li>
</ul>
Preferred Experience:
<ul>
<li>Experience with advanced biologics modalities (e.g., bispecifics, fusion proteins, ADCs, monoclonal antibodies).</li>
<li>Familiarity with digital tools for process monitoring and data analytics.</li>
<li>Prior experience in a fast-paced biotech or a global pharmaceutical environment.</li>
</ul>
Company DescriptionA top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints. Job Responsibilities: •\tConducting Post Market Activities and Post Market Surveillance •\tManaging Customer and Product Complaint Investigation programs Education and Experience: •\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry •\tBachelor's degree •\tComputer proficiency 
<h3>Company Description</h3>
A top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints.\r\nJob Responsibilities:\r\n•\tConducting Post Market Activities and Post Market Surveillance\r\n•\tManaging Customer and Product Complaint Investigation programs\r\nEducation and Experience:\r\n•\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry\r\n•\tBachelor's degree\r\n•\tComputer proficiency

Head of Biologics MSAT

<h3>Job Description</h3>
Job Description
Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve. Cleanroom Technician &nbsp;
<ul>
<li>Schedule: M-F, 6:30am-3pm -OR- 7am-3:30pm</li>
</ul>
 Description: Responsibility for performing functions in a cleanroom associated with all microfluidic chip manufacturing operations in a high-volume, fast-paced environment, the ideal candidate must be able to accomplish assignments that are routine in nature. Duties and Responsibilities:
<ul>
<li>Work in a high-volume microfluidic fabrication lab:</li>
<li>Operates workstation activities in a wafer manufacturing or test area devoted to both production and process development. Processes include - lithography, wet benches, pick and place, epoxy dispensing, UV curing, packaging, dicing, drilling, test equipment and substrate bonding</li>
<li>Performs production processes in accordance with documented specifications and production schedules</li>
<li>Adheres to all safety and clean room specifications</li>
<li>Interacts with other team members toward the solution of problems and the fulfillment of manufacturing objectives and participates in natural work group teams for continuous improvement</li>
<li>Performs other duties as assigned</li>
</ul>
 Basic Qualifications:
<ul>
<li>High school diploma or equivalent</li>
<li>2+ years of clean room experience</li>
<li>Must have ability to use a microscope</li>
</ul>
 Preferred Qualifications:
<ul>
<li>Ability to communicate effectively in a group as well as on an individual level.</li>
<li>Ability to work cooperatively as part of a team with people of various educational and technical backgrounds</li>
<li>Ability to read and interpret specifications, procedures, and mathematics</li>
<li>Ability to read and write English</li>
<li>Computer skills and familiarity with Microsoft Windows, Word and Excel</li>
<li>Familiar with basic laboratory safety and cleanroom protocol</li>
</ul>
 Physical Requirements: Must have ability to:
<ul>
<li>work in a Class 100 &amp; 1000 clean room</li>
<li>wear a full clean room suit, covered from head to toe</li>
<li>handle chemicals, including hydrofluoric acid, which requires safety glasses, a face shield, apron and gloves</li>
<li>stand and/or walk for up to 4 hours at a time</li>
<li>lift up to 10lbs and push/pull up to 20 pounds</li>
</ul>
Company DescriptionConnexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve. 
<h3>Company Description</h3>
Connexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve.

Cleanroom Technician

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The QC Microbiology Supervisor will lead, plan, organize, guide, and be responsible for the coordination/performance of the QC Microbiology Laboratory Operations,
This position is located in Lexington, MA and will supervise the 2nd shift which will operate M-F from 1:00-9:30pm. The Supervisor will report to the Manager of Microbiology.
ESSENTIAL JOB FUNCTIONS
<ul>
<li>Oversee the execution of monitoring for controlled environments and utility systems within the Manufacturing Facility. Ensure execution is compliant with appropriate regulatory requirements and guidelines using approved Standard Operating procedures (SOPs). </li>
<li>Serve as an SME and provide guidance and support for critical QC Microbiology assays and methods.</li>
<li>Provide leadership, coaching, mentoring and training of QC Microbiology staff, aiding in employee development and performance. </li>
<li>Ensure QC Microbiology testing is completed, reviewed, and reported in a compliant manner and results are timely delivered to clients.</li>
<li>Maintain all aspects of QC Microbiology day-to-day operations and scheduling to align with all aspects of GXP requirements.</li>
<li>Manage data and trending in support of environmental monitoring and utility monitoring reports.</li>
<li>Represent QC Microbiology at cross-functional meetings and interact with internal customers, clients and external vendors.</li>
<li>Perform QC Microbiology testing as required, including bioburden, endotoxin of in-process, product and utility samples. </li>
<li>Perform EM and utility related monitoring, as necessary. </li>
<li>Identify continuous improvement opportunities. Design, implement and maintain resulting systems.</li>
<li>Ensure a safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies is maintained.</li>
<li>Author and revise SOPs, protocols and technical reports to meet industry standards, as necessary.</li>
<li>Oversee QC sample submission and processing activities, and ensure testing is performed accordingly. </li>
<li>Initiate and collaborate on change controls, deviations, and Out of Specification (OOS), Out of Tolerance (OOT) investigations related to QCM and assist with non-conformance investigations. </li>
<li>Serve a system owner of QC Microbiology controlled temperature units, respond per on-call schedule to CMS alarms, including off-hours and weekends </li>
</ul>
SPECIAL WORK REQUIREMENTS
<ul>
<li>Ability to troubleshoot equipment and microbiological testing methods.</li>
<li>Ability to adapt to schedules and priorities changes based on business needs</li>
<li>Experience creating comprehensive department schedules</li>
<li>Leadership experience within a high functioning team</li>
<li>Other duties, as assigned. </li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
Bachelor's degree in microbiology; other related science will be considered. 
Essential
ON-THE-JOB EXPERIENCE

5-15 years of Microbiology laboratory-based experience in a QC testing capacity within a cGMP setting. 
Required
Prior supervisory experience. 
Desired
SKILLS / ABILITIES

Excellent microbiological skills and technical experience in GXP environment. 
Essential
Thorough understanding of industry and regulatory testing requirements for QC Microbiology.
Essential
Computer literacy (MS Word, Excel, and LIMS)
Essential
Must possess excellent communication and organizational skills.
Essential
Detail-Oriented
Essential
Self-organized
Essential
Work Environment:
<ul>
<li>Regularly sit or stand for long periods of time </li>
<li>Work in a BSL 2 environment</li>
</ul>
Movement:
<ul>
<li>Work in a BSL 2 environment</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 25 pounds </li>
</ul>
Vision
<ul>
<li>Frequently utilize close vision and the ability to adjust focus</li>
</ul>
Communication
<ul>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

QC Supervisor, Microbiology (2nd Shift, 1pm-9:30pm)

<h3>Job Description</h3>
Job Description
Scientific Marketing Manager / Director - in vivo Pharmacology
Location: Remote, USA
Salary: $120,000 - $160,000
 
Combine your passion for science with creativity in scientific marketing.
Join our dynamic marketing team at Pharmaron as a Scientific Marketing Manager. We are seeking an individual who is passionate about drug discovery and preclinical development with experience in drug efficacy testing in disease models. Become part of our team to help us elevate our brand and drive sales.
 
Your Key Responsibilities:
<ul>
<li>Craft compelling narratives: Translate complex scientific concepts into engaging stories that resonate with our audience.</li>
<li>Create new content: Partner with our scientists to create engaging content that showcases our expertise such as brochures, white papers, flyers, webpage content, etc.</li>
<li>Lead marketing campaigns: Develop and execute multi-channel campaigns that increase brand awareness and generate leads.</li>
<li>Analyze and optimize: Track marketing performance, identify trends, and refine our strategies for maximum impact.</li>
<li>Represent our brand: Manage our presence at industry conferences and events.</li>
</ul>
 Your Profile:
<ul>
<li>Location: Remote, the applicant must be located in Europe or North America.</li>
<li>Scientific background: A degree in biology, pharmacology, veterinary medicine or a related field is essential.</li>
<li>Experience: Minimum of 5 years of industry experience related to animal disease models in drug discovery or drug development.</li>
<li>Exceptional communication skills: A passion for writing and the ability to convey complex scientific ideas to diverse audiences.</li>
<li>Passion for learning: A desire to stay updated on industry trends and best practices.</li>
<li>Collaborative spirit: Enjoy working with cross-functional teams and external partners with a willingness to travel as needed.</li>
</ul>
 
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&amp;D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
Insurance including Medical, Dental &amp; Vision with significant employer contributions
Employer-funded Health Reimbursement Account
Healthcare &amp; Dependent Care Flexible Spending Accounts
100% Employer-paid Employee Life and AD&amp;D Insurance, Short and Long Term Disability Insurance
401k plan with generous employer match
Access to an Employee Assistance Program
How to Apply:
 
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
 
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
 
#LI-EH1

Scientific Marketing Manager / Director - in vivo Pharmacology / Toxicology

<h3>Job Description</h3>
Job Description
About Mass Audubon Mass Audubon is the largest nature-based conservation organization in New England. Founded in 1896 by two women who fought for the protection of birds, Mass Audubon carries on their legacy by focusing on the greatest challenges facing the environment today: the loss of biodiversity, inequitable access to nature, and climate change. With the help of our 160,000 members and supporters, we protect wildlife, conserve and restore resilient land, advocate for impactful environmental policies, offer nationally recognized education programs for adults and children, and provide endless opportunities to experience the outdoors at our wildlife sanctuaries. Explore, find inspiration, and take action at massaudubon.org. 
About This Position The Senior Director of Conservation Science (Senior Director) is an exciting, highly-influential role responsible for providing science-based leadership in support of Mass Audubon’s commitment to address our climate and biodiversity crisis across the Commonwealth and serve as a model for the nation. The role will define and lead the organization’s scientific agenda and priorities using an evidence-based approach that relies on data, research, and applied science to guide Mass Audubon’s conservation actions and policies. This position is a member of Mass Audubon’s Conservation Division and reports to the Chief Conservation Officer.
This role oversees all aspects of the organization’s scientific endeavors including identifying conservation issues and priorities, providing authoritative, technical leadership and collaborating with internal and external partners to design and implement solutions. The conservation scope of this role is broad and extends from addressing the ecological health and resilience of Mass Audubon’s wildlife sanctuary network to positioning Mass Audubon to tackle broader conservation challenges such as biodiversity loss, climate change and inequitable access to nature in our region. As such, a successful candidate will have substantive scientific knowledge and will maintain a perspective and professional network at the regional, state, national, and international levels in relevant disciplines.
This Senior Director serves as the organization’s lead scientific ambassador and spokesperson and as such is a vocal champion of Mass Audubon’s ecological assets and science-based strategies. They will develop key partnerships with public and private organizations to identify, resolve, and communicate solutions and best practices. The candidate must possess strong communication skills that support effective interactions with scientists, partners, colleagues, staff, governance, and volunteers. In addition, they will also serve as a scientific resource to conservation partners, foundations, the academic community, and the government agencies of the Commonwealth.
Equally important in an ideal candidate is the ability to lead and manage people and to motivate a diverse community of individuals towards mission-based goals. The Senior Director oversees an experienced, decentralized team of scientific experts in terrestrial and coastal ecology and restoration as well as data analytics and management. In addition, the role collaborates with peer departments to achieve a full range of conservation strategies and holds relationships with academic and NGO partners to support a focused research portfolio that supports Mass Audubon’s conservation agenda. The Senior Director leads this broad team in the design and implementation of adaptive, successful conservation plans that serve as a roadmap for on-the-ground action at multiple scales.
This role provides the opportunity for an experienced, results-driven, conservation professional to provide a leading voice on the critical conservation issues facing Massachusetts and New England. As a senior leader in the organization, this position will contribute to the design of organizational initiatives and strategies, implementation of strategic program plans, and establishment of organizational operating policies and positions. Application Instructions Please submit a resume and cover letter. Only applications with these materials will be reviewed.
Responsibilities Core Responsibilities of this position include: 
Scientific Direction &amp; Leadership Provide overall scientific direction and leadership to the organization by identifying and framing priority, mission-core conservation issues and driving solutions through organizational goals, strategies, and policies. Contribute scientific expertise and perspective to strategy and program design, implementation, and evaluation. 
Program Delivery &amp; Implementation Achieve annual and multi-year strategic goals through management of a conservation project portfolio, the oversight of a suite of conservation science programs and successful internal and external collaborations. Elevate conservation impact by driving conservation projects, supporting organizational strategy and informing policy priorities. Apply a data driven, analytical approach to program evaluation and bring innovation to program design and evolution.
Technical Leadership Serve as – and support a team of – technical experts in applied conservation science that are considered ‘best in class’. Stay current with the evolving body of research and practice by maintaining an internal learning culture and a vibrant external exchange with NGO, public agency, and academic partners. Contribute to the field of practice by promoting outcomes in applied ecological management, coordinating a focused, outcome-driven research agenda and community science framework, and developing new data and information management systems. 
Team Management Manage and develop the conservation science team to support the ecological management priorities of our sanctuaries and to address the greatest conservation issues of our time. Prioritize professional development and team building and support individual and team performance through annual and multi-year work plans framed by measurable goals and outcomes.
The Senior Director has oversight of the Conservation Science Department, which includes the Ecological Management and Restoration Teams, the Climate-Smart Forestry Team, conservation operations and the GIS Team. In addition, the role collaborates closely with Land Conservation, Bird Conservation, Advocacy &amp; Policy, Education, Wildlife Sanctuaries, and is supported by the central administrative departments. 
Resource Development and Management Focus and grow Mass Audubon’s conservation science impact through exceptional budget and grants management as well as resource development, including cultivation of public and private funding opportunities. 
Additional Responsibilities:
<ul>
<li>Serve as a charismatic spokesperson for Mass Audubon’s mission and goals among a wide range of audiences</li>
<li>Support communications and outreach with governance and leadership donors</li>
<li>Build internal awareness and a learning environment around conservation best practice </li>
<li>Maintain and evolve a set of conservation science-related policies and public issue statements and ensure that they are consistently applied across the organization’s operations</li>
</ul>
Qualifications At Mass Audubon, our highest priority is finding the best candidate for the job. Research has shown that people of color and women are less likely to apply for jobs if they don’t believe they meet every one of the qualifications described in a job description. We encourage you to apply, even if you don't believe you meet every one of our described qualifications or you have a less traditional background. We are looking for applicants with the following qualifications:
<ul>
<li>Strong scientific understanding stemming from an advanced degree in natural sciences, ecology, or related field and/or at least 10 years of experience in natural resources management, conservation research, or other natural science-based endeavor</li>
<li>Knowledge of North American ecosystems (specifically the Northeast) is a plus</li>
<li>Strong analytical skills and familiarity with a range of tools, methodologies and systems including GIS, spatial analytics, and data management systems</li>
<li>Demonstrated ability to lead individuals and teams in setting priorities and designing strategies, goals, and implementation plans that address critical conservation issues; experience with leadership in a non-profit organization is a plus</li>
<li>Proven ability to organize, inspire, and support people with diverse backgrounds and different reporting relationships to create a common program or shared result</li>
<li>Proven business acumen including a results-driven perspective and the ability to develop and analyze plans and budgets and to meet deadlines and goals in a fast-paced work environment</li>
<li>Demonstrated experience in the recruitment, effective management, and development of a high-performing team of staff and volunteers</li>
<li>Proven ability to develop and nurture a deep network of relationships in the government, nonprofit and academic sectors and to manage strong relationships with funders</li>
<li>Exceptional communication skills (written and oral) and a proven comfort with sharing scientific concepts with a broad range of audiences</li>
<li>Ability to collaborate as a dominant working style</li>
<li>A valid driver’s license and the physical capacity to travel frequently and extensively within the state and region</li>
</ul>
Compensation, Benefits and Perks This position’s pay range is $140,000-$150,000 per year; actual salary will reflect level of experience and qualifications relative to position requirements. Benefits eligible staff at Mass Audubon may elect to enroll in medical, dental, and vision plans. Mass Audubon also offers disability and life insurance plans, a retirement plan through MetLife, and Flexible Spending Account options. Mass Audubon employment also includes access to an Employee Assistance Program (EAP) and the Reciprocity Agreement through the Consortium of Non-Profit Arts/Cultural/Environmental Organizations of New England. Mass Audubon employees also enjoy 13 paid holidays (holidays may shift annually due to where days fall within calendar).
Work Schedule Full-time schedule of 40 hours per week, Monday through Friday.
Other Requirements Employees must successfully complete a CORI and SORI Background Check and a Motor Vehicle Record (if applicable) is required.
Mass Audubon’s Commitment to Diversity, Equity, Inclusion, &amp; Justice Mass Audubon embraces diversity and equal opportunity in a serious way. We are dedicated to forming a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. People of color are strongly encouraged to apply. 
Mass Audubon’s mission is to “protect the nature of Massachusetts for people and for wildlife” by building a strong coalition of employees, volunteers, and community members. We recognize that the environmental movement and field of conservation have been affected by societal systems that have limited opportunity and access for many people. As a result, Mass Audubon is committed to creating an inclusive environment for all employees and applicants. We are engaged in an ongoing process of organizational assessment and change, designed to remove barriers and create a workplace where all forms of diversity are recognized and valued. 
Equal Employment Opportunity Statement Mass Audubon is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and applicants. Mass Audubon 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. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Senior Director of Conservation Science

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJoin a team where science meets purpose!
We’re looking for a detail-oriented and driven Analytical Chemist to support critical testing operations in a fast-paced pharmaceutical environment. If you're passionate about precision, thrive in a collaborative setting, and are ready to make an immediate impact, we want to hear from you.
What You’ll Do
<ul>
<li>Perform routine and advanced chemical testing using cutting-edge techniques and instruments.</li>
<li>Operate and maintain specialized lab equipment including HPLC, GC, ICP, and more.</li>
<li>Lead and support investigations to troubleshoot and resolve analytical issues.</li>
<li>Ensure strict adherence to cGMP standards, data integrity, and documentation practices.</li>
<li>Collaborate with cross-functional teams to support raw material testing and product release.</li>
</ul>
What You Bring
<ul>
<li>Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.</li>
<li>Hands-on experience in the pharmaceutical or biotechnology industry.</li>
<li>Proficiency with analytical instruments such as HPLC, GC, and ICP.</li>
<li>A strong understanding of regulatory compliance and quality standards.</li>
</ul>
Why Join Us?
<ul>
<li>Be part of a mission-driven organization focused on improving patient outcomes.</li>
<li>Work in a collaborative, innovation-focused environment.</li>
<li>Gain exposure to advanced technologies and industry-leading practices.</li>
</ul>
Pay and Benefits
The pay range for this position is $65000.00 - $80000.00/yr.
Health Vision 401 K Dental Relocation Assistant
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Jun 30, 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.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
esponsibilities:
<ul>
<li>Perform routine and non-routine analytical assays to support raw materials, in-process samples, product release, and stability under supervision, following established SOPs</li>
<li>Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations</li>
<li>Accurately record experimental data and observations in compliance with GxP standards.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in chemistry, Biochemistry, Pharmaceutical Sciences, or a related field. Seeking a recent graduate with Coop/Internship experience.</li>
<li>0 to 2 years of experience in a GMP/GLP regulated laboratory environment, with exposure to pharmaceutical or biotechnology industries preferred</li>
<li>Understanding of analytical techniques and their application in raw materials, in-process testing, release, and stability studies is preferred</li>
<li>Experience in HPLC, GC, MS or wet/analytical chemistry</li>
</ul>
Why Choose R&amp;D Partners?
As an employee, you have access to a comprehensive benefits package including:
<ul>
<li>Medical insurance – PPO, HMO &amp; HSA</li>
<li>Dental &amp; Vision insurance</li>
<li>401k plan</li>
<li>Employee Assistance Program</li>
<li>Long-term disability</li>
<li>Weekly payroll</li>
<li>Expense reimbursement</li>
<li>Online timecard approval</li>
</ul>
Pay Scale:
$62,400/annually
R&amp;D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research &amp; engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&amp;D Partners is an equal-opportunity employer.
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

QC Chemist I

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
We are seeking a motivated and detail-oriented Research Associate – Analytical R&amp;D to join our team. This role supports ongoing research and development efforts by performing routine analytical testing, assisting with data analysis and documentation, and operating advanced laboratory instrumentation. The ideal candidate is eager to learn, technically skilled, and committed to maintaining quality and safety in a collaborative lab environment.
Key Responsibilities:
<ul>
<li>Perform routine analytical tests independently, following established protocols and procedures.</li>
<li>Support activities related to Corrective and Preventive Actions (CAPA), System Suitability Testing (SST), and Analytical Quality Management (AQM).</li>
<li>Prepare samples and mobile phases using techniques such as solid-phase extraction (SPE), liquid–liquid extraction (LLE), and supported liquid extraction (SLE).</li>
<li>Operate and assist in the maintenance and troubleshooting of advanced laboratory instruments, including:
<ul>
<li>Agilent: UPLC, SQ, TOF, QTOF</li>
<li>Thermo: UPLC, Duo LC, Orbitrap</li>
</ul>
</li>
<li>Analyze and interpret data with guidance, applying foundational knowledge of method parameters and system performance.</li>
<li>Assist in method development and sample preparation experiments under the direction of senior scientists.</li>
<li>Document all lab activities accurately and in a timely manner using electronic laboratory notebooks and internal systems.</li>
<li>Contribute to lab operations by helping maintain equipment, supplies, and shared responsibilities for cleanliness, organization, and compliance.</li>
<li>Collaborate effectively with team members to support ongoing projects, safety standards, and data integrity.</li>
<li>Actively participate in training opportunities and expand technical skills through hands-on learning.</li>
</ul>
Qualifications 
Minimum Requirements:
<ul>
<li>B.S. or M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related scientific discipline</li>
<li>3–4 years of industry experience in an analytical or bioanalytical laboratory setting</li>
<li>Hands-on experience operating, troubleshooting, and maintaining LC-MS systems, including HPLC, UPLC, and LCMS platforms</li>
<li>Proficiency with Agilent UPLC instrumentation and OpenLab ChemStation software</li>
<li>Familiarity with mobile phase preparation and common sample preparation techniques</li>
<li>Understanding of Automated Quality Management (AQM) systems and basic statistical analysis</li>
<li>Experience performing System Suitability Testing (SST) and interpreting results</li>
<li>Strong collaboration and communication skills; able to work effectively in cross-functional team environments</li>
<li>Ability to manage multiple tasks and adapt in fast-paced, changing environments</li>
<li>Demonstrated problem-solving skills, willingness to learn, and attention to detail</li>
<li>Commitment to laboratory safety protocols and data integrity</li>
<li>Must be authorized to work in the United States without restriction or sponsorship</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with advanced LC-MS instruments, including:
<ul>
<li>Agilent: SQ, TOF, QTOF</li>
<li>Thermo: UPLC, Duo LC, Orbitrap</li>
</ul>
</li>
<li>Familiarity with software platforms such as MassHunter, Xcalibur, or Chromeleon</li>
<li>Prior experience supporting or executing:
<ul>
<li>CAPA investigations (Corrective and Preventive Actions)</li>
<li>Method development and validation</li>
<li>RNA and oligonucleotide analysis</li>
</ul>
</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Onsite Meeting with Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Research Technician - Analytical R&D

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
This role involves performing routine analytical testing, supporting data analysis and documentation, operating advanced lab instruments, and collaborating with the team to maintain quality and safety standards.
Responsibilities include:&nbsp;
<ul>
<li>Independently perform assigned analytical tasks under minimal supervision, including support for Corrective and Preventive Actions (CAPA), System Suitability Testing (SST), and Analytical Quality Management (AQM) activities.</li>
<li>Conduct routine analytical activities, including but not limited to sample and mobile phase preparation, using a variety of techniques such as solid-phase extraction (SPE), liquid–liquid extraction (LLE), and supported liquid extraction (SLE), in accordance with established protocols.</li>
<li>Operate and perform complex troubleshooting on laboratory instrumentation, such as Agilent UPLC, SQ, TOF, and QTOF systems as well as Thermo UPLC, Duo LC, and Orbitrap platforms.</li>
<li>Execute data analysis and reporting, applying foundational knowledge of parameters needed for accurate data processing and reduction.</li>
<li>Support and execute experiments for method development and sample preparation studies by following protocols and documenting results in collaboration with senior team members.</li>
<li>Contribute to the improvement of standard procedures, including preparation protocols and basic sample quality control techniques.</li>
<li>Maintain accurate and timely documentation of laboratory activities, including experiments, results, and observations, in electronic laboratory notebooks and systems.</li>
<li>Collaborate with team members to support daily lab operations and quality initiatives, including compliance with safety, data integrity, and lab standards.</li>
<li>Proactively identify technical training needs to enhance skills and actively participate in hands-on learning of analytical techniques and laboratory best practices</li>
</ul>
Qualifications 
Minimum Requirements:
<ul>
<li>B.S. or M.S. in Analytical Chemistry, Biochemistry, Chemistry, or a related field with 3-4 years of industry experience&nbsp;</li>
<li>Hands-on expertise in troubleshooting and maintaining LC-MS systems.</li>
<li>Experience troubleshooting and maintaining&nbsp;LC systems: HPLC, UPLC, LCMS</li>
<li>Hands-on experience with&nbsp;Agilent UPLC&nbsp;instruments</li>
<li>Proficiency with&nbsp;OpenLab ChemStation&nbsp;software</li>
<li>Familiarity with&nbsp;mobile phase preparation&nbsp;techniques</li>
<li>Knowledge of&nbsp;Automated Quality Management (AQM)&nbsp;and related statistical analysis</li>
<li>Experience performing&nbsp;System Suitability Testing (SST)&nbsp;and interpreting associated statistics</li>
<li>Strong collaboration skills with cross-functional teams.</li>
<li>Ability to manage multiple priorities and adapt in dynamic environments.</li>
<li>Demonstrated scientific problem-solving, learning agility, and effective communication (written and verbal).</li>
<li>Strong adherence to safety protocols.</li>
<li>Authorized to work in the U.S. without restriction or sponsorship.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with instruments:
<ul>
<li>Agilent: SQ, TOF, QTOF systems</li>
<li>Thermo: UPLC, Duo LC, Orbitrap platforms</li>
</ul>
</li>
<li>Experience with software:
<ul>
<li>MassHunter,&nbsp;Xcalibur,&nbsp;Chromeleon</li>
</ul>
</li>
<li>Experience with methods:
<ul>
<li>CAPA&nbsp;(Corrective and Preventative Actions)</li>
<li>Method development and validation</li>
<li>RNA analysis</li>
<li>Oligonucleotide analysis</li>
</ul>
</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Onsite Meeting with Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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